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Investigations on the organic drift in North Swedish streams
Limitations of Using Microsoft Excel Version 2016 (MS Excel 2016) for Statistical Analysis for Medical Research
Phloem necrosis of coffee in Surinam
Anatomy of Mystus seenghala IV Nervous system
Integrated farming system for gardenland conditions of Coimbatore district - an over view
Tetrapleure (Tetrapleura tetraptera), an unknown African medicinal and spice plant
The origin and phylogenetic significance of the trochophoran larvae 2. evolutionary significance of the larvae of coelomate worms and mollusks
Comparison of rice bran and maize bran as feeds for growing and fattening pigs
Enterobacter amnigenus. An unusual human pathogen
Influence of Seriboost foliar application on leaf yield and leaf protein content in mulberry (Morus spp.), in relation to silkworm cocoon production
The identity of the lipstick mold of cultivated mushrooms agaricus bisporus
Advantages and disadvantages of bordeaux mixture and of lime-sulphur used on apples in the growing season
'Pan-sukh' disease of Rice in the Central Provinces
Geological age of the Ptilophyllum flora; a critical reassessment
Study of vitellogenesis in birds; physiological phases & role of folliculin in vitellogenesis
Evaluation of WCT coconut and Komadan coconut
Therapy for acne with saccharomyces boulardii
Evidence for Late Cretaceous N-S dextral shear in the west-central crystalline core, North Cascades, Washington
'Rajeshwari' - a high-yielding white seeded variety of sesame for Andhra Pradesh
Manufacture of Ricotta cheese from whey fortified with skim milk powder using different acidulants
Occurrence of Eutrichophilus mexicanus (Rudow, 1866) and Eutrichophilus lobatus (Ewing, 1936) (Phthiraptera: Trichodectidae) on Sphiggurus villosus (Cuvier, 1825) (Rodentia: Erethizontidae) in Rio de
Factors affecting fruitfulness in durian (Durio zibethinus Murr.). I. Flowering and pollination
Bronchial cuff pressure change caused by left-sided double-lumen endobronchial tube displacement
Some Biological Applications of Organometallic Compounds
The composition of pampas-grass (Cortaderia argentea.)

List of PDF Full Texts available from EurekaMag Chapter 43111

Chapter 43111 contains a list of PDF Full Texts available from EurekaMag.




Familial cervical lung hernia: a report of 4 cases in a family
, Zhonghua Jie he He Hu Xi Za Zhi 17(4): 230 (1994)

Familial changes in L.D.H. isoenzymes associated with a myopathic syndrome in one case and with angina and normal coronary arteries in another
, Revue Neurologique 129(4): 173-184 (1973)

Familial character of Shereshevskiĭ-Turner syndrome with karyotype 45, XO-46, XX
, Problemy Endokrinologii 16(3): 44-45 (1970)

Familial character of pulmolithiasis endoalveolaris diffusa. (Microlithiasis alveolaris pulmonum)
, Zeitschrift für Erkrankungen der Atmungsorgane Mit Folia Bronchologica 132(1): 31-38 (1970)

Familial characteristics of Class II, division 2. Clinical study
, Revue d'Orthopedie Dento-Faciale 8(1): 59-66 (1974)

Familial cheiroarthropathy without juvenile onset diabetes mellitus
, Rheumatology International 2(3): 141-143 (1982)

Familial childhood parathyroid adenoma
, Journal of Pediatric Surgery 29(12): 1530-1531 (1994)

Familial chloride diarrhea-chloride malabsorption
, Bibliotheca Paediatrica 87: 137-149 (1968)

Familial chloride diarrhoea (congenital alkalosis with diarrhoea)
, Australian Paediatric Journal 8(4): 187-190 (1972)

Familial choanal atresia in a rhinoplasty candidate--a case report
, Eye Ear Nose and Throat Monthly 52(6): 222-226 (1973)

Familial choices and procreative behavior of the clientele of familial planning centers
, Gynecologie Pratique 23(2): 77-87 (1972)

Familial cholestasis with gallstone, ataxia and visual disturbance
, Tohoku Journal of Experimental Medicine 137(2): 137-144 (1982)

Familial chondrocalcinosis and HLA system
, Arthritis and Rheumatism 24(12): 1590-1591 (1981)

Familial chondrocalcinosis. Prevalence in Northern Spain and clinical features in five pedigrees
, Arthritis and Rheumatism 23(4): 471-478 (1980)

Familial chorioretinal vascular anastomoses and congenital cataracts
, Journal of Pediatric Ophthalmology and Strabismus 17(6): 384-388 (1980)

Familial choroideremia
, Bulletins et Memoires de la Societe Francaise d'Ophtalmologie 85(0): 321-334 (1972)

Familial chromosomal aberrations. I
, Annales Paediatrici. International Review of Pediatrics 206(5): 317-332 (1966)

Familial chromosomal aberrations. II
, Annales Paediatrici. International Review of Pediatrics 206(6): 381-395 (1966)

Familial chronic biologic false-positive seroreactions for syphilis. Report of two families, one with three generations affected
, JAMA 219(1): 45-48 (1972)

Familial chronic discoid lupus erythematosus and hypergammaglubulinemia
, Revista Clinica Espanola 105(4): 329-330 (1967)

Familial chronic encephalopathy with convulsive seizures, disturbance in gait, postural changes and dementia--a contribution to the study of atypical brain atrophy
, Seishin Shinkeigaku Zasshi 68(9): 1043-1059 (1966)

Familial chronic interstitial nephropathy and retinal dystrophy (Senior-Loken syndrome)
, La Nouvelle Presse Medicale 3(6): 309-312 (1974)

Familial chronic jaundice caused by nonspherocytic hemolytic anemia, with increase of erythrocyte pyruvate kinase
, Revista Clinica Espanola 123(2): 167-172 (1971)

Familial chronic lymphatic leukemia associated with cutaneous epithelioma
, Il Fracastoro 61(3): 269-273 (1968)

Familial chronic lymphocytic leukemia
, Annals of Internal Medicine 71(2): 279-284 (1969)

Familial chronic mucocutaneous candidiasis successfully treated with oral ketoconazole
, South African Medical Journal 59(7): 237-239 (1981)

Familial chronic mucocutaneous candidiasis. Study of 2 families
, Medicina Cutanea Ibero-Latino-Americana 12(1): 33-40 (1984)

Familial chronic myelogenous leukemia. Report of 3 cases in a family
, Sangre 27(5): 953-958 (1982)

Familial chronic myeloid leukaemia
, Lancet 2(8404): 699 (1984)

Familial chronic nephritis
, Proceedings of the Royal Society of Medicine 60(3): 246-247 (1967)

Familial chronic neutropenia with bone marrow maturation arrest
, Harefuah 78(3): 103-106 (1970)

Familial chronic non-hemolytic jaundice (Dubin-Johnson syndrome). Clinical and histological study in a premature twin
, Pathologica 59(869): 35-41 (1967)

Familial chronic pancreatitis associated with pancreatic lithiasis
, American Journal of Surgery 127(5): 511-517 (1974)

Familial chronic thyroiditis and its similarity to myotonic dystrophy
, Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 69(1): 27-32 (1980)

Familial chronic tubulointerstitial nephritis with antibodies to the tubular basement membrane
, Pediatrie 37(5): 371-381 (1982)

Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity
, Journal of Lipid Research 24(1): 12-19 (1983)

Familial cirrhosis with autoimmune features and raised immunoglobulin levels
, Gastroenterology 59(4): 546-552 (1970)

Familial cirsoid aneurysm of the scalp
, Journal of Neurology Neurosurgery and Psychiatry 34(6): 664-667 (1971)

Familial clinical patterns. I. Reported symptoms and signs in the dentist and his wife
, Geriatrics 25(2): 123-126 (1970)

Familial clustering case of hepatitis delta
, Kansenshogaku Zasshi. Journal of the Japanese Association for Infectious Diseases 69(6): 747-751 (1995)

Familial clustering in Paget's disease
, Medicina Clinica 81(16): 736-737 (1983)

Familial clustering in Paget's disease of bone: an epidemiological perspective of interest
, Medicina Clinica 81(2): 60-63 (1983)

Familial clustering in Paget's disease: etiopathogenic implications. Presentation of a family with 12 affected members
, Medicina Clinica 81(2): 43-46 (1983)

Familial clustering of HTLV-I infection in southeastern Italy
, Lancet 346(8968): 179-180 (1995)

Familial clustering of atrioventricular canal defects
, American Heart Journal 108(1): 175-177 (1984)

Familial clustering of hepatitis B antigen: a study in relatives of patients with liver diseases and hepatitis B antigenaemia
, British Medical Journal 3(5929): 495-497 (1974)

Familial clustering of leprosy patients in an Israeli village
, Leprosy Review 53(4): 277-283 (1982)

Familial clustering of nasopharyngeal carcinoma
, Cancer 46(10): 2325-2327 (1980)

Familial clustering of situs inversus totalis, and asplenia and polysplenia syndromes
, American Journal of Medical Genetics 16(1): 43-47 (1983)

Familial clustering of tonsillectomies and adenoidectomies
, Clinical Pediatrics 19(4): 276-283 (1980)

Familial coexistence of Stargardt's disease and pigmented retinal degeneration
, Annali di Ottalmologia E Clinica Oculistica 94(7): 787-792 (1968)

Familial coexistence of chronic inflammatory polyarthropathy with sacro-iliac joint involvement
, Revue du Rhumatisme et des Maladies Osteo-Articulaires 37(3): 213-224 (1970)

Familial coexistence of dyschromatopsia and tapetoretinal degeneration
, Bulletin des Societes d'Ophtalmologie de France 82(5): 645-647 (1982)

Familial cold urticaria. A generalized reaction involving leukocytosis
, Archives of Internal Medicine 124(2): 129-134 (1969)

Familial cold urticaria. Apropos of a case
, Revue du Rhumatisme et des Maladies Osteo-Articulaires 49(2): 131-135 (1982)

Familial cold urticaria: a father and daughter with typical clinical and laboratory features
, Annals of Allergy Asthma and Immunology: Official Publication of the American College of Allergy Asthma and Immunology 74(4): 295-298 (1995)

Familial colon carcinoma
, Nederlands Tijdschrift Voor Geneeskunde 128(17): 796-800 (1984)

Familial colon polyposis
, Nordisk Medicin 86(38): 1111 (1971)

Familial colonic cancer syndromes
, Western Journal of Medicine 139(3): 351-359 (1983)

Familial colonic polyposis. 2 case reports
, Srpski Arhiv Za Celokupno Lekarstvo 108(9): 943-948 (1980)

Familial colorectal cancer and hereditary brachydactyly
, British Medical Journal 282(6274): 1431-1432 (1981)

Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and management
, Current Problems in Pediatrics 24(9): 295-305 (1994)

Familial combined hyperlipoproteinemia. Evidence for a role of growth hormone deficiency in effecting its manifestation
, Journal of Clinical Investigation 65(4): 829-835 (1980)

Familial combined hyperlipoproteinemia: studies in 91 adults and 95 children from 33 kindreds
, Metabolism, Clinical and Experimental 23(2): 1403-1428 (1973)

Familial comedones (a case report)
, Indian Journal of Dermatology 20(1): 6-7 (1974)

Familial communicational patterns of a patient with Gilles-De-La-Tourette syndrome
, Journal of Nervous and Mental Disease 154(1): 60-68 (1972)

Familial concentration of ischaemic heart disease
, British Medical Journal 2(5543): 4-5 (1967)

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy
, Neuromuscular Disorders: Nmd 5(3): 227-231 (1995)

Familial concurrence of myasthenia gravis and rheumatoid arthritis
, Archives of Internal Medicine 125(6): 1056-1058 (1970)

Familial condensing osteopathy with leontiasis ossium
, Archives Francaises de Pediatrie 29(4): 447 (1972)

Familial conditions of xeroderma pigmentosum in Algeria
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 77(6): 837-841 (1970)

Familial conduction disturbance
, American Journal of Cardiology 30(4): 450-451 (1972)

Familial congenital Cushing's syndrome due to bilateral nodular adrenal hyperplasia
, Clinical Endocrinology 14(5): 519-526 (1981)

Familial congenital adrenal hypoplasia
, Helvetica Paediatrica Acta 28(4): 277-282 (1973)

Familial congenital adrenal hypoplasia with failure of the adrenal cortex
, Verhandlungen der Deutschen Gesellschaft für Pathologie 52: 481-485 (1968)

Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings
, Pediatric Radiology 14(5): 323-327 (1984)

Familial congenital coralliform cataract
, American Journal of Optometry and Physiological Optics 51(10): 770-773 (1974)

Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment
, American Journal of Medical Genetics 17(2): 471-483 (1984)

Familial congenital disorder resembling stiff-man syndrome
, American Journal of Diseases of Children 124(5): 730-731 (1972)

Familial congenital duodenal atresia
, Pediatrics 46(4): 629-632 (1970)

Familial congenital dysproteinemia
, Pediatria Panamericana 10(3): 92-94 (1965)

Familial congenital epidermolytic hyperkeratosis confined to the palms and soles
, Southern Medical Journal 67(9): 1126-1128 (1974)

Familial congenital esophageal atresia. Personal case report and review of the literature
, Human Genetics 66(2-3): 260-266 (1984)

Familial congenital factor V deficiency (parahemophilia)
, Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 54(7): 816-820 (1965)

Familial congenital generalized fibromatosis in two half-sisters
, Schweizerische Medizinische Wochenschrift 101(38): 1381-1385 (1971)

Familial congenital glaucoma with dominant heredity
, Acta Ophthalmologica 46(3): 459-462 (1968)

Familial congenital heart block and hydrops fetalis
, Archives of Disease in Childhood 55(6): 479-480 (1980)

Familial congenital heart defects
, Sovetskoe Zdravookhranenie Kirgizii 3: 58-59 (1972)

Familial congenital heart disease. II. Chromosomal studies
, Circulation 34(3): 517-523 (1966)

Familial congenital hypoaldosteronism caused by 18-OH-dehydrogenase deficiency
, Pediatric Research 2(6): 456-463 (1968)

Familial congenital hypoplasia of the thumb--report on a family
, Journal of Hand Surgery 9(2): 145-148 (1984)

Familial congenital hypothyroidism without goiter
, Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 23(3): 199-205 (1971)

Familial congenital occurrence of multiple odontomas
, Deutsche Zahnarztliche Zeitschrift 28(5): 628-632 (1973)

Familial congenital ocular motor apraxia
, Neurology 20(4): 405 (1970)

Familial congenital ocular motor apraxia and immune deficiency
, Archives of Neurology 37(5): 325 (1980)

Familial congenital pseudarthrosis of the ulna
, Journal of Hand Surgery 20(3): 331-332 (1995)

Familial congenital short small bowel with associated defects. A long-term survival
, Clinical Pediatrics 23(8): 453-455 (1984)

Familial congenital spherocytosis
, Revista Chilena de Pediatria 54(5): 340-344 (1983)

Familial congestion of a Zenker diverticulum
, Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 112(3): 411-412 (1970)

Familial congestive cardiomyopathy
, Terapevticheskii Arkhiv 55(10): 75-76 (1983)

Familial congestive cardiomyopathy with positive rheumatoid factor. Report of one family
, Japanese Circulation Journal 46(3): 303-309 (1982)

Familial congestive-dilatative type of cardiomyopathy
, Zhonghua Nei Ke Za Zhi 19(1): 42-44 (1980)

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects
, Seminars in Hematology 4(3): 233-240 (1967)

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia
, Seminars in Hematology 4(3): 241-249 (1967)

Familial continual desquamation
, Annales de Dermatologie et de Venereologie 110(2): 141-143 (1983)

Familial continual skin peeling
, British Journal of Dermatology 81(3): 191-195 (1969)

Familial copper deficiency
, Orvosi Hetilap 123(30): 1855-1857 (1982)

Familial corneal degeneration--type Reis-Bücklers
, Klinika Oczna 83(10-12): 515-518 (1981)

Familial corneal scarring: a new dystrophy?
, Ophthalmology 91(2): 174-178 (1984)

Familial correlates of the 14 and 6 cps EEG positive spike pattern
, Psychiatric Research Reports 20: 121-131 (1966)

Familial correlational analyses, sex differences, and the X-linked gene hypothesis
, Psychological Bulletin 93(3): 427-440 (1983)

Familial cosegregation of manic-depressive illness and a form of hereditary cerebellar ataxia
, American Journal of Medical Genetics 60(3): 206-209 (1995)

Familial cranio-metaphyseal dysplasia
, Revue du Rhumatisme et des Maladies Osteo-Articulaires 33(12): 714-726 (1966)

Familial craniosynostosis with oral anomalies
, Developmental Medicine and Child Neurology 12(3): 315-320 (1970)

Familial cretinism with goiter--an inborn metabolic error
, Ceskoslovenska Pediatrie 23(2): 134-137 (1968)

Familial cryoglobulinemia and C4 deficiency
, Scandinavian Journal of Rheumatology 13(2): 151-154 (1984)

Familial cutaneous amyloidosis with systemic manifestations in males
, American Journal of Medical Genetics 10(1): 65-75 (1981)

Familial cutaneous leiomyoma
, Indian Journal of Pathology and Bacteriology 16(3): 75-77 (1973)

Familial cutaneous leiomyomas and their association with uterine myoma. Study of a 3-generation pedigree
, Medicina Cutanea Ibero-Latino-Americana 11(2): 133-138 (1983)

Familial cutaneous leiomyomatosis
, Journal of the American Academy of Dermatology 4(4): 430-434 (1981)

Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus
, Proceedings of the National Academy of Sciences of the United States of America 80(19): 6071-6075 (1983)

Familial cutaneous mastocytosis
, Anais Brasileiros de Dermatologia 45(4): 317-324 (1970)

Familial cutaneous papillomatosis
, Archives of Dermatology 92(4): 394-395 (1965)

Familial cystinuria in Ioannina District (Greece). Diagnosis and treatment
, Urological Research 11(6): 291-296 (1983)

Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure
, Archives of Disease in Childhood 56(9): 715-721 (1981)

Familial de Lange syndrome with chromosome abnormalities
, Pediatrics 37(1): 92-101 (1966)

Familial de Lange syndrome. Report of three cases in a sibship
, Clinical Genetics 2(3): 170-176 (1971)

Familial deafness with osteo-onycho-dysplasia
, Journal de Genetique Humaine 18(1): 101-108 (1970)

Familial defect dysproteinemia with antibody deficiency syndrome
, Das Deutsche Gesundheitswesen 22(47): 2212-2220 (1967)

Familial defect of platelet adhesion and aggregation
, Medicina 30(4): 330-348 (1970)

Familial deficiency of C5 in humans: intact but deficient alternative complement pathway activity
, Clinical Immunology and Immunopathology 21(1): 62-76 (1981)

Familial deficiency of C7 associated with adrenomyeloneuropathy
, Revue Neurologique 150(1): 78-80 (1994)

Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes
, Klinische Wochenschrift 49(23): 1294-1298 (1971)

Familial deficiency of apolipoproteins A-I and C-III and precocious coronary-artery disease
, New England Journal of Medicine 306(25): 1513-1519 (1982)

Familial deficiency of factor X
, Sangre 18(2): 178-189 (1973)

Familial deficiency of prostacyclin production stimulating factor in the hemolytic uremic syndrome of childhood
, Thrombosis Research 21(3): 311-315 (1981)

Familial deficiency on alpha-1-antitrypsin
, Zeitschrift für Kinderheilkunde 110(2): 115-127 (1971)

Familial deficit of antithrombin III and mitral valve prolapse
, Medicina Clinica 83(1): 43 (1984)

Familial degeneration of the anterior cornea
, Klinika Oczna 44(7): 707-710 (1974)

Familial degeneration of the conduction system
, Giornale Italiano di Cardiologia 3(4): 519-529 (1973)

Familial delayed development of speech
, Otolaryngologia Polska 20(2): 367-371 (1966)

Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity
, Clinical Pediatrics 8(8): 453-458 (1969)

Familial dementia of adult onset with pathological findings of a 'non-specific' nature
, Brain: a Journal of Neurology 104(Pt 1): 61-78 (1981)

Familial depression versus depression identified in a control group: are they the same?
, Psychological Medicine 25(4): 797-806 (1995)

Familial dermal cylindroma with involvement of the parotid gland
, British Journal of Plastic Surgery 35(2): 167-170 (1982)

Familial dermatoglyphic analysis in syndactyly type I
, Journal of Hand Surgery 6(6): 537-542 (1981)

Familial developmental coxa vara
, Clinical Orthopaedics and Related Research 86: 2-5 (1972)

Familial diabetes according to our observations
, Pediatria Polska 42(3): 315-320 (1967)

Familial diabetes insipidus of central origin
, La Nouvelle Presse Medicale 10(11): 897-899 (1981)

Familial diabetes mellitus and optic atrophy
, Irish Medical Journal 73(5): 211-212 (1980)

Familial diabetic xanthomatosis
, Vestnik Dermatologii i Venerologii 1985(9): 45-47 (1985)

Familial differences in schizophrenia with good and poor prognosis
, Psychological Medicine 1(4): 326-332 (1971)

Familial differentiation, individualization, and sexuality in early adolescence: exploratory study
, Contraception Fertilite Sexualite 23(5): 341-347 (1995)

Familial diffuse interstitial pulmonary fibrosis
, Medicina Clinica 80(13): 590-591 (1983)

Familial diffuse polyposis of the colon and rectum: supplementary report on three pedigrees
, Diseases of the Colon and Rectum 16(6): 517-523 (1973)

Familial diffuse polyposis of the large intestine
, Meditsinskaia Sestra 40(6): 21-23 (1981)

Familial dilated (congestive) cardiomyopathy. Occurrence in two brothers and an overview of the literature
, South African Medical Journal 66(1): 26-30 (1984)

Familial dilated cardiomyopathy
, American Journal of Cardiology 54(3): 456-457 (1984)

Familial diphosphoglycerate mutase deficiency: hematological and biochemical study
, Nouvelle Revue Francaise d'Hematologie 12(3): 269-287 (1972)

Familial discoid lupus erythematosus
, Actas Dermo-Sifiliograficas 57(11): 357-364 (1966)

Familial discoid lupus erythematosus associated with heterozygote C2 deficiency
, Arthritis and Rheumatism 23(8): 898-903 (1980)

Familial discoid lupus erythematosus associated with heterozygous C4 deficiency
, Acta Dermato-Venereologica 64(6): 552-554 (1984)

Familial disease characterized by neonatal jaundice, and probable hepatosteatosis and kernicterus: a new syndrome?
, Pediatrics 51(2): 192-198 (1973 )

Familial disease characterized by the association of a nonprogressive ataxic gait, palmar telangiectasis and hypogammaglobulinemia
, Archivos de Neurobiologia 33(2): 233-236 (1970)

Familial disease with ulcero-mutilans acropathia, pyramidal syndrome and debility
, Journal de Medecine de Lyon 51(184): 925-935 (1970)

Familial disorders of defective mental development and amyosthemia with diffuse slow spike and waves in electroencephalography (congenital carbohydrate metabolism disorders?)
, Seishin Shinkeigaku Zasshi 73(7): 572-583 (1971)

Familial disorders of thyroxin-binding globulin as a cause of misleading serum thyroxin values. A study of 6 families
, Schweizerische Medizinische Wochenschrift 104(33): 1141-1147 (1974)

Familial disposition for leftside abomasum displacement in cattle
, DTW, Deutsche Tieraerztliche Wochenschrift 81(18): 430-433 (1974)

Familial dissecting aneurysm complicating Marfan's syndrome
, American Heart Journal 78(4): 577-578 (1969)

Familial dissecting aneurysm of the aorta
, Archiv für Kreislaufforschung 63(3): 288-319 (1970)

Familial disseminated atypical mycobacterial disease
, Immunology Letters 43(1-2): 133-138 (1994)

Familial disseminated atypical mycobacterial infection in childhood
, Lancet 345(8955): 993 (1995)

Familial disseminated lupus erythematosus
, Revista Clinica Espanola 118(2): 179-182 (1970)

Familial disseminated piliform hyperkeratosis
, Annales de Dermatologie et de Syphiligraphie 99(4): 381-390 (1972)

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
, Journal of the Neurological Sciences 51(1): 141-155 (1981)

Familial distribution of Australian antigen in the Chilean population
, Revista Medica de Chile 101(10): 758-762 (1973)

Familial distribution of cholesterolemia, arterial blood pressure and relative weight
, Sozial- und Praventivmedizin 25(4): 162-165 (1980)

Familial distributions of organ specific antibodies in the blood of patients with Addison's disease and hypoparathyroidism and their relatives
, Clinical and Experimental Immunology 5(5): 461-468 (1969)

Familial ductus arteriosus. (Apropos of 3 cases seen in the same family)
, Marseille Medical 103(1): 51-54 (1966)

Familial duodenal atresia
, Archives of Disease in Childhood 45(240): 281-282 (1970)

Familial duodenal diverticulosis
, Revista Espanola de Las Enfermedades del Aparato Digestivo 34(2): 195-198 (1971)

Familial dwarfism with high IR-GH: report of two affected sibs with genetic and epidemiologic considerations
, Human Genetics 59(4): 367-372 (1981)

Familial dynamics and mental retardation
, Archivos de Neurobiologia 37(2): 99-112 (1974)

Familial dynamics in a case of anorexia nervosa
, Rivista Sperimentale di Freniatria E Medicina Legale Delle Alienazioni Mentali 96(1): 143-152 (1972)

Familial dysalbuminemic hyperthyroxinemia (FDH): inadequacy of the "analog" methods for assaying free-T4 levels
, European Journal of Nuclear Medicine 9(6): 284-285 (1984)

Familial dysalbuminemic hyperthyroxinemia: a study of four probands and the kindred of three
, Clinical Chemistry 30(7): 1179-1181 (1984)

Familial dysalbuminemic hyperthyroxinemia: a syndrome that can be confused with thyrotoxicosis
, New England Journal of Medicine 306(11): 635-639 (1982)

Familial dysautonomia
, New England Journal of Medicine 274(4): 207-209 (1966)

Familial dysautonomia
, Birth Defects Original Article Series 7(1): 202-204 (1971)

Familial dysautonomia (Riley-Day syndrome): report of case
, Asdc Journal of Dentistry for Children 51(1): 64-65 (1984)

Familial dysautonomia (Riley-Day): aural histopathology
, Practica Oto-Rhino-Laryngologica 30(3): 194-200 (1968)

Familial dysautonomia associated with recurrent osteomyelitis in a non-Jewish girl
, Journal of Pediatrics 96(1): 75-77 (1980)

Familial dysautonomia differentiated from related disorders. Case reports and discussions of current concepts
, Pediatrics 37(3): 435-446 (1966)

Familial dysautonomia or the Riley-Day syndrome
, Developmental Medicine and Child Neurology 9(2): 234-235 (1967)

Familial dysautonomia. A cineradiographic study of the swallowing mechanism
, Radiology 90(1): 107-112 (1968)

Familial dysautonomia. Apropos of a case
, Pediatrie 21(8): 943-956 (1966)

Familial dysautonomia: a case report
, Asdc Journal of Dentistry for Children 38(6): 409-411 (1971)

Familial dysautonomia: diagnosis, pathogenesis and management
, Advances in Pediatrics 21: 75-96 (1974)

Familial dysautonomia: some aspects of treatment for the paediatric dental practitioner
, Dental Practitioner and Dental Record 20(10): 345-346 (1970)

Familial dysautonomy (Riely-Day's syndrome). A review and report of a characteristic case
, Ugeskrift for Laeger 144(33): 2403-2407 (1982)

Familial dysbetalipoproteinemia
, Harefuah 106(4): 174-175 (1984)

Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cows
, Journal of Clinical Investigation 68(4): 1075-1085 (1981)

Familial dysbetalipoproteinemia. New aspects of pathogenesis and diagnosis
, Medical Clinics of North America 66(2): 441-454 (1982)

Familial dyschondrosteosis. Study of 3 cases (mother and her 2 sons)
, La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 44(41): 2474-2479 (1968)

Familial dysenzymatic goiter caused by failure in he binding of iodothyroxines
, Revista Argentina de Endocrinologia y Metabolismo 12(4): 227-233 (1966)

Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen
, Pathologie-Biologie 22(Suppl): 72-79 (1974)

Familial dysfibrinogenemia--"Detroit fibrinogen"
, Verhandlungen der Deutschen Gesellschaft für Innere Medizin 74: 140-144 (1968)

Familial dysfibrinogenemia; fibrinogen Haarlem I and II
, Nederlands Tijdschrift Voor Geneeskunde 125(19): 734-737 (1981)

Familial dysgammaglobulinemia in a case of lupous erythematovisceritis
, Il Policlinico. Sezione Pratica 75(46): 1515-1521 (1968)

Familial dysgenesis of the vermis: a syndrome of hyperventilation, abnormal eye movements and retardation
, Neurology 18(3): 302-303 (1968)

Familial dyslipoproteinemia
, Rinsho Byori. Japanese Journal of Clinical Pathology 31(2): 117-120 (1983)

Familial dysplasia epiphysealis hemimelica, associated with chondromas and osteochondromas. Report of a kindred with variable presentations
, Journal of Bone and Joint Surgery. American Volume 56(7): 1513-1516 (1974)

Familial dystonia with atrophy of the putamen and caudate nuclei detected by CT scan--biochemical study of catecholamine metabolism
, Rinsho Shinkeigaku 23(7): 585-591 (1983)

Familial dystrophic nanism with Hirschsprung's disease
, Annales de Pediatrie 16(8): 496-502 (1969)

Familial dystrophic periodic shedding of the nails
, Cutis 25(6): 622-623 (1980)

Familial early hypoparathyroidism associated with hypomagnesaemia
, Acta Paediatrica Scandinavica 59(6): 715-719 (1970)

Familial early infantile myasthenia gravis with a 15-year follow-up
, Journal of the Neurological Sciences 8(3): 573-578 (1969)

Familial early profound deafness in an Athabascan kindred
, Alaska Medicine 24(2): 18-19 (1982)

Familial early-onset nephrotic syndrome: diffuse mesangial sclerosis. Clinico-pathological study of a kindred
, Acta Paediatrica Scandinavica 71(5): 753-758 (1982)

Familial ectrodactyly and polydactyly: variable expressivity of one single gene--embryological considerations
, Clinical Genetics 22(4): 206-210 (1982)

Familial effects in schizophrenia and homosexuality
, Australian and New Zealand Journal of Psychiatry 6(2): 116-119 (1972)

Familial effects on plasma sex-steroid content in man: testosterone, estradiol and Sex-hormone-binding globulin
, Metabolism, Clinical and Experimental 31(1): 6-9 (1982)

Familial electrophysiological observation in pigmentary degeneration of the retina with or without consanguinity
, Nippon Ganka Gakkai Zasshi 72(8): 1218-1231 (1968)

Familial elevation of serum thyroxine-binding globulin capacity
, Acta Endocrinologica 60(1): 130-136 (1969)

Familial elevations of total and free thyroxine in healthy, euthyroid subjects without detectable binding protein abnormalities
, Acta Endocrinologica 100(2): 224-230 (1982)

Familial emphysema
, American Review of Respiratory Disease 98(4): 692-696 (1968)

Familial emphysema and alpha-1-antitrypsin deficiency
, New England Journal of Medicine 275(23): 1301-1304 (1966)

Familial emphysema associated with antitrypsin deficiency
, Diseases of the Chest 55(4): 285-289 (1969)

Familial emphysema with reduction of the antitrypsin capacity of the serum
, Lyon Medical 227(10): 911-920 (1972)

Familial encephalo-retinal dysplasia (Krause-Reese-Syndrome) with myoclonic-astatic petit mal seizures
, Zeitschrift für Kinderheilkunde 103(2): 81-89 (1968)

Familial encephalopathy with generalized vascular malformations of the dolicho-artery type
, Pediatrie 21(7): 763-767 (1966)

Familial encephalopathy with hyperuricemia. A study of purine metabolism and therapeutic attempts
, Archives Francaises de Pediatrie 26(2): 139-154 (1969)

Familial encephalopathy with hyperuricemia. Study of purine metabolism. Therapeutic endeavors
, Archives Francaises de Pediatrie 25(8): 968 (1968)

Familial encephalopathy with oligophrenia and congenital indifference to pain and Laurence-Moon-Bardet-Biedl syndrome
, Annales Medico-Psychologiques 2(4): 545-564 (1970)

Familial encephalopathy, imino-glycinuria, hydroxyprolinemia
, Archives Francaises de Pediatrie 29(4): 336-337 (1972)

Familial endemic persistent atrial standstill in a small mountain community: review of eight cases
, European Heart Journal 4(5): 354-361 (1983)

Familial endocrine adenomatosis with associated Zollinger-Ellison syndrome. Wermer's syndrome
, American Journal of Surgery 115(5): 695-701 (1968)

Familial endocrine tumors
, Western Journal of Medicine 132(4): 352-353 (1980)

Familial enteric neurofibromatosis
, Medical Times 94(5): 544-548 (1966)

Familial enteropathic acrodermatitis
, Vestnik Dermatologii i Venerologii 42(12): 53-58 (1968)

Familial enzymologic study in viral hepatitis
, Rivista di Clinica Pediatrica 81(6): 1150-1154 (1968)

Familial eosinophilia
, Wiadomosci Lekarskie 27(2): 153-156 (1974)

Familial epidemic occurrence of tularemia
, Wiadomosci Lekarskie 25(20): 1843-1847 (1972)

Familial epidemic of hepatitis of probable toxoplasmic etiology
, Medicina 32(1): 15-22 (1972)

Familial epidemics of tick-borne encephalitis in central Povazie
, Bratislavske Lekarske Listy 95(11): 523-526 (1994)

Familial epidermodysplasia verruciformis of Lewandowsky and Lutz
, Archives of Dermatology 105(1): 73-78 (1972)

Familial epilepsy and progressive partial lipodystrophy. (Barraquer-Simons disease)
, Epilepsia 10(1): 87-90 (1969)

Familial epilepsy and yellow teeth--a disease of the CNS associated with enamel hypoplasia
, Helvetica Paediatrica Acta 29(4): 283-294 (1974)

Familial epilepsy through four generations. An EEG and clinical study of the parents and the 11 children of a sibship
, Epilepsia 10(1): 77-82 (1969)

Familial episode of Reovirus type I infection of an enteritic nature
, Archivio Italiano di Scienze Mediche Tropicali E di Parassitologia 47(11): 303-314 (1966)

Familial episodic ataxia
, Der Nervenarzt 51(6): 355-358 (1980)

Familial epithelial corneal dystrophy
, Klinische Medizin; Osterreichische Zeitschrift für Wissenschaftliche und Praktische Medizin 21(10): 555-556 (1966)

Familial epithelial dystrophy of the cornea
, Klinische Monatsblatter für Augenheilkunde 148(6): 869-873 (1966)

Familial erythrocyte ATP: pyruvate phosphotransferase deficiency
, Acta Haematologica Polonica 13(3-4): 157-163 (1982)

Familial erythrocytosis among the residents of the Chuvash ASSR
, Problemy Gematologii i Perelivaniia Krovi 19(10): 30-33 (1974)

Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln)
, Mayo Clinic Proceedings 46(11): 721-727 (1971)

Familial erythrocytosis with over-production of erythropoietin
, Clinical and Laboratory Haematology 5(4): 335-342 (1983)

Familial erythrocytosis. A description of three families, one with hemoglobin Ypsilanti
, Annals of Internal Medicine 69(4): 769-776 (1968)

Familial erythroleukemia: four cases of the Diguglielmo syndrome in close relatives
, Johns Hopkins Medical Journal 150(1): 1-9 (1982)

Familial erythrophagic lymphohistiocytosis. Report of a family case
, Sangre 25(3): 380-386 (1980)

Familial erythrophagocytic lymphohistiocytosis in infancy
, European Journal of Pediatrics 136(2): 223-225 (1981)

Familial erythrophagocytic lymphohistiocytosis with neonatal presentation
, Anales Espanoles de Pediatria 17(2): 112-118 (1982)

Familial erythrophagocytic lymphohistiocytosis. Report of five cases with cytophotometric study of nuclear DNA
, Annales de Pathologie 2(2): 127-132 (1982)

Familial erythrophagocytic lymphohistiocytosis: an association with serum lipid abnormalities
, Journal of Pediatrics 102(2): 270-273 (1983)

Familial erythrophagocytic lymphohistiocytosis: treatment with vinblastine-loaded platelets
, Cancer 46(12): 2566-2570 (1980)

Familial erythrophagocytic reticulosis. Complete response to combination chemotherapy
, Archives of Disease in Childhood 59(2): 173-175 (1984)

Familial esophageal carcinoma
, Revista de la Facultad de Ciencias Medicas de Cordoba 26(2): 215-218 (1968)

Familial essential hypercholesterinemia and pregnancy
, Zeitschrift für die Gesamte Innere Medizin und ihre Grenzgebiete 21(5): 156-160 (1966)

Familial essential hyperprolinemia
, La Presse Medicale 79(21): 945-948 (1971)

Familial essential myoclonus
, Brain: a Journal of Neurology 97(1): 131-138 (1974)

Familial essential trigeminal neuralgia
, Rivista di Neurobiologia: Organo Ufficiale Della Societa Dei Neurologi Neuroradiologi e Neurochirurghi Ospedalieri 28(3-4): 299-302 (1982)

Familial etiology of hirsutism
, Folia Endocrinologica 24(5): 406-411 (1971)

Familial etiology of pulp stones
, Acta Stomatologica Belgica 68(1): 133-139 (1971)

Familial etiology of schizophrenia: is a scientific methodology possible?
, Psychological Bulletin 66(3): 214-227 (1966)

Familial euthyroid hyperthyroxinemia resulting from increased thyroxine binding to thyroxine-binding prealbumin
, New England Journal of Medicine 306(16): 966-969 (1982)

Familial euthyroid thyroxine excess: an appropriate response to abnormal thyroxine binding associated with albumin
, Journal of Clinical Endocrinology and Metabolism 53(2): 353-359 (1981)

Familial euthyroid thyroxine excess: characterization of abnormal intermediate affinity thyroxine binding to albumin
, Journal of Clinical Endocrinology and Metabolism 55(2): 244-250 (1982)

Familial evolutive characteristic of hemolytic disease caused by anti-Rh isoimmunization
, La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 42(19): 1183-1193 (1966)

Familial excess of cancer of the ovary and other anatomic sites
, JAMA 245(3): 261-264 (1981)

Familial exfoliative cheilitis
, Vestnik Dermatologii i Venerologii 42(9): 75-78 (1968)

Familial external genital ambiguity due to a transformation defect of androgen-receptor complexes that is expressed with 5 alpha-dihydrotestosterone and the synthetic androgen methyltrienolone
, American Journal of Medical Genetics 18(3): 493-507 (1984)

Familial extra centric bisatellited chromosome
, Cytogenetics 8(3): 177-186 (1969)

Familial extragonadal germ cell tumors
, American Journal of Medical Genetics 15(1): 175-176 (1983)

Familial exudative vitreoretinopathy and hereditary retinal vascular tortuosity
, Journal Francais d'Ophtalmologie 18(3): 231-237 (1995)

Familial exudative vitreoretinopathy associated with familial thrombocytopathy
, British Journal of Ophthalmology 67(11): 755-758 (1983)

Familial exudative vitreoretinopathy. An expanded view
, Archives of Ophthalmology 86(2): 150-155 (1971)

Familial facial asymmetry (autosomal dominant hemihypertrophy?)
, Oral Surgery Oral Medicine and Oral Pathology 50(4): 321-324 (1980)

Familial factor in reno-ureteral malformations
, Journal Belge de Radiologie 53(6): 454-459 (1970)

Familial factors affecting arterial blood gas values and respiratory chemosensitivity in chronic obstructive pulmonary disease
, American Review of Respiratory Disease 125(4): 420-425 (1982)

Familial factors and perinatal problems in idiopathic childhood epilepsy
, Archives of Disease in Childhood 48(4): 324 (1973)

Familial factors in adenocarcinoma of the colon
, Cancer 28(1): 46-50 (1971)

Familial factors in cancer of the genitourinary tract
, Recent Results in Cancer Research. Fortschritte der Krebsforschung. Progres Dans les Recherches sur le Cancer 136: 306-321 (1994)

Familial factors in epilepsy
, Marseille Medical 105(5): 449-451 (1968)

Familial factors in mortality with control of epidemiological covariables. Swedish twins born 1886-1925
, Acta Geneticae Medicae et Gemellologiae 33(3): 403-412 (1984)

Familial factors in peptic ulcer. I. The occurrence of ulcer in relatives
, American Journal of Epidemiology 91(5): 453-459 (1970)

Familial factors in peptic ulcer. II. Family structure in duodenal ulcer
, American Journal of Epidemiology 91(5): 460-466 (1970)

Familial factors in premature coronary heart disease--a preliminary report from the Tecumseh Community Health Study
, American Journal of Epidemiology 91(3): 233-237 (1970)

Familial factors in schizophrenia
, Wiadomosci Lekarskie 36(5): 381-383 (1983)

Familial factors in suicide
, Diseases of the Nervous System 34(2): 90-93 (1973)

Familial factors in the etiology of carcinoma of the large bowel
, Proceedings of the Royal Society of Medicine 67(8): 751-752 (1974)

Familial factors predisposing to benzolic involutive myelopathy
, Il Fracastoro 61(3): 274-278 (1968)

Familial factors, ventilatory control, and sudden infant death
, New England Journal of Medicine 302(9): 517-519 (1980)

Familial false-positive serological reactions in syphilis
, Vestnik Dermatologii i Venerologii 1984(4): 73-74 (1984)

Familial farmer's lung
, Lancet 1(7707): 1022 (1971)

Familial fatal lymphoproliferative disease with histiocytosis and hemophagocytosis
, Verhandlungen der Deutschen Gesellschaft für Pathologie 67: 372-379 (1983)

Familial favus in the district Magdeburg and its therapy with griseofulvin
, Dermatologische Wochenschrift 152(19): 465-470 (1966)

Familial fibrocystic pulmonary dysplasia: a new case in a known affected family
, Canadian Medical Association Journal 94(20): 1059-1061 (1966)

Familial fibrosing alveolitis
, Irish Journal of Medical Science 150(7): 204-209 (1981)

Familial fibrous dysplasia of jaws (cherubism)
, Pediatrie 25(3): 331-334 (1970)

Familial fibula amyotrophies of neurogenic origin
, Les Cahiers de Medecine 12(10): 803-815 (1971)

Familial fistulae of the lacrimal sac
, Klinika Oczna 44(3): 273-276 (1974)

Familial fleck retina with night blindness
, Annals of Ophthalmology 14(9): 836-841 (1982)

Familial florid papillomatosis of the nipple
, Annals of Surgery 175(2): 254-256 (1972)

Familial focal His bundle tachycardia. A new case in the same family
, Annales de Pediatrie 31(4): 343 (1984)

Familial focal His tachycardia
, Annales de Pediatrie 30(2): 107-111 (1983)

Familial focal facial dermal dysplasia
, Archives of Dermatology 107(4): 591-595 (1973)

Familial focal segmental glomerulosclerosis
, International Journal of Pediatric Nephrology 4(4): 231-234 (1983)

Familial foramina parietalia permagna: five cases in a family
, No to Shinkei 32(5): 523-531 (1980)

Familial form of Crohn's disease
, Les Cahiers de Medecine 15(6): 305-310 (1974)

Familial form of De Morsier-Kalmann's syndrome
, La Nouvelle Presse Medicale 10(11): 909-910 (1981)

Familial form of Leber's miliary retinal angiomatosis
, Bulletin des Societes d'Ophtalmologie de France 74(12): 1163-1167 (1974)

Familial form of Rokitansky-Kuster-Hauser syndrome
, Bulletin de la Federation des Societes de Gynecologie et Dobstetrique de Langue Francaise 18(3): 229-234 (1966)

Familial form of atrio-ventricular conduction disorders. Apropos of a case of syncopal atrioventricular block in a 21-month-old child. Pacemaker implantation
, Annales de Cardiologie et d'Angeiologie 22(4): 331-337 (1973)

Familial form of basilar impression
, Schweizer Archiv für Neurologie Neurochirurgie und Psychiatrie 104(1): 30-42 (1969)

Familial form of congenital virilizing adrenal cortex hyperplasia
, Problemy Endokrinologii 27(2): 41-43 (1981)

Familial form of ectodermal dysplasia
, Polski Tygodnik Lekarski 28(7): 256-258 (1973)

Familial form of esophageal achalasia in children
, L'Union Medicale du Canada 94(10): 1293-1300 (1965)

Familial form of hepatic porphyria
, Vrachebnoe Delo 1981(1): 19-20 (1981)

Familial form of incontinentia pigmenti
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 76(6): 791-792 (1969)

Familial form of pyknodysostosis with hematologic manifestations in a child
, Archives de Pediatrie: Organe Officiel de la Societe Francaise de Pediatrie 2(5): 456-459 (1995)

Familial form of retracted and chronic condensation of the middle pulmonary lobe with alpha-1-antitrypsin deficiency: genetic study
, Journal Francais de Medecine et Chirurgie Thoraciques 23(5): 469-487 (1969)

Familial form of subacute spinal amyotrophy. Anatomo-clinical study
, Revue Neurologique 126(1): 70-76 (1972)

Familial form of total digestive aganglionosis with absence of nerve fibers
, Archives Francaises de Pediatrie 40(10): 781-783 (1983)

Familial forms of cancer of the stomach
, Archives Francaises des Maladies de l'Appareil Digestif 56(9): 827-840 (1967)

Familial forms of chromaffinomas
, Problemy Endokrinologii 29(3): 40-43 (1983)

Familial forms of frontotemporal dementia
, Nederlands Tijdschrift Voor Geneeskunde 139(32): 1661-1662 (1995)

Familial forms of intracranial cavernous hemangioma. Apropos of 5 cases in 2 families
, Neuro-Chirurgie 29(4): 263-269 (1983)

Familial forms of megaloblastic anemias
, Schweizerische Medizinische Wochenschrift 100(46): 1961-1963 (1970)

Familial forms of scoliosis (clinical aspects)
, Ortopediia Travmatologiia i Protezirovanie 31(4): 22-26 (1970)

Familial fragility on chromosome 16 (fra 16q22) enhanced by both interferon and Distamycin A
, Human Genetics 63(4): 341-344 (1983)

Familial frequency of congenital aniridia
, Klinische Monatsblatter für Augenheilkunde 150(4): 550-551 (1967)

Familial frontonasal dermoid cysts. Report of four cases
, Journal of Neurosurgery 34(5): 683-686 (1971)

Familial fructose and galactose intolerance
, Lancet 2(7782): 872 (1972)

Familial fructose intolerance
, Pediatria Polska 49(9): 1143-1147 (1974)

Familial fugue--a case report
, Canadian Journal of Psychiatry. Revue Canadienne de Psychiatrie 28(8): 654-656 (1983)

Familial functional antithrombin III deficiency
, Scandinavian Journal of Haematology 24(2): 105-109 (1980)

Familial fundus flavimaculatus
, Bulletins et Memoires de la Societe Francaise d'Ophtalmologie 86(0): 86-89 (1973)

Familial ganglioneuromatous polyposis of the large bowel. Report of a family with associated juvenile polyposis
, American Journal of Surgical Pathology 8(7): 515-520 (1984)

Familial gastric polyposis. A new entity
, Journal de Genetique Humaine 28(3): 293-297 (1980)

Familial gastro-duodenal ulcers
, La Revue du Praticien 23(49): 4395-4400 (1973)

Familial gastroschisis and omphalocele
, American Journal of Human Genetics 34(3): 517-518 (1982)

Familial gastroschisis in siblings is rare
, Journal of Pediatric Surgery 29(12): 1637-1638 (1994)

Familial generalized colonic polyposis
, Journal Belge de Radiologie 54(1): 45-51 (1971)

Familial genetic studies in neuroarthritic diathesis in children
, Pediatriia 1980(2): 47-50 (1980)

Familial genetically determined rickets with aminoaciduria
, Pediatria Polska 43(8): 1007-1012 (1968)

Familial genitocolonic cancer syndrome
, Revue Medicale de Liege 39(22): 805-815 (1984)

Familial giant cell hepatitis. Report of two cases and review of the literature
, Archives of Pathology 95(4): 240-244 (1973)

Familial giardiasis: clinical and epidemiological study beginning with index cases
, Revista Medica de Chile 110(3): 224-227 (1982)

Familial gingival fibromatosis of possible dysgenopathic origine
, Rivista Italiana di Stomatologia 21(12): 1349-1365 (1966)

Familial gingival fibromatosis: an unusual pathology
, Journal of Oral Pathology 1(2): 76-83 (1972)

Familial glaucoma
, L'Union Medicale du Canada 99(6): 1102-1105 (1970)

Familial glaucoma associated with elevated episcleral venous pressure
, Archives of Ophthalmology 80(2): 202-208 (1968)

Familial glaucoma. In nine generations of a South Hampshire family
, British Journal of Ophthalmology 58(5): 536-542 (1974)

Familial glioblastoma
, Arquivos de Neuro-Psiquiatria 53(2): 312-317 (1995)

Familial glioma
, Indian Pediatrics 31(12): 1576-1579 (1994)

Familial gliomas. Report of four cases
, Journal of Neurosurgery 37(1): 110-112 (1972)

Familial gliomas: report of four families, with chromosome studies
, Neurosurgery 10(4): 445-449 (1982)

Familial glomangiomatosis
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 79(1): 41-44 (1972)

Familial glomerulo-tubular nephropathy with the de Toni-Debré-Fanconi syndrome
, Archives Francaises de Pediatrie 25(1): 43-69 (1968)

Familial glomerulonephritis characterized by massive deposits of fibronectin
, American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 25(5): 781-791 (1995)

Familial glomerulonephritis following streptococcal infection
, Polski Tygodnik Lekarski 26(20): 748-751 (1971)

Familial glomus tumors: clinical and genetic aspects
, Acta Oto-Rhino-Laryngologica Belgica 35(1): 50-55 (1981)

Familial glucose-6-phosphate dehydrogenase deficiency
, Pediatrie 27(3): 314-316 (1972)

Familial glutathione reductase deficiency and disorder of glutathione synthesis in the erythrocyte
, Helvetica Paediatrica Acta 25(5): 542-552 (1970)

Familial glycosphingolipoidosis of the dog (Juvenile amaurotic idiocy)
, Ergebnisse der Allgemeinen Pathologie und Pathologischen Anatomie 47: 1-43 (1966)

Familial goiter accompanying amblyacousia and idiocy
, Horumon to Rinsho. Clinical Endocrinology 21(2): 187-191 (1973)

Familial goiter and congenital deafness
, Revista de la Sociedad Peruana de Endocrinologia 2(1): 38-47 (1965)

Familial goiter due to an organification defect in euthyroid siblings
, Journal of Clinical Endocrinology and Metabolism 27(8): 1137-1140 (1967)

Familial goiter with dimished synthesis of thyroglobulin
, Zeitschrift für die Gesamte Experimentelle Medizin Einschliesslich Experimentelle Chirurgie 150(3): 203-212 (1969)

Familial goitre with absence of thyroglobulin and synthesis of thyroid hormones from thyroidal albumin
, Journal of Endocrinology 60(3): 389-397 (1974)

Familial goitrous cretinism
, Indian Pediatrics 9(11): 697-702 (1972)

Familial gonadal neoplasms
, New England Journal of Medicine 309(22): 1389 (1983)

Familial gouty malignant uric acid lithiasis due to mutant phosphoribosylpyrophosphate synthetase
, Der Urologe. Ausg. a 12(4): 153-157 (1973)

Familial granulomatous arteritis with polyarthritis of juvenile onset
, New England Journal of Medicine 306(2): 86-90 (1982)

Familial granulovacuolar lobular myopathy with electrical myotonia
, Journal of the Neurological Sciences 56(2-3): 133-140 (1982)

Familial group diseases caused by Microsporum canis Bodin 1902 in the district of Dresden
, Dermatologische Monatschrift 159(4): 391-397 (1973)

Familial growth retardation with isolated thyroid-stimulating hormone deficiency
, Clinical Pediatrics 23(12): 675-678 (1984)

Familial haemolytic anaemia due to pyruvate kinase deficiency
, Folia Medica Neerlandica 14(2): 72-76 (1971)

Familial haemolytic anaemia with erythrocyte inclusion bodies, bilifuscinuria and abnormal haemoglobin (haemoglobin Galliera Genova)
, British Journal of Haematology 11(5): 511-517 (1965)

Familial haemophagocytic lymphohistiocytosis in two brothers: possible relationship between impaired immune function and clinical picture of graft-versus-host disease
, European Journal of Pediatrics 142(4): 306-307 (1984)

Familial haemophagocytic reticulosis
, Archives of Disease in Childhood 43(231): 601-606 (1968)

Familial haemophagocytic reticulosis in first cousins
, Archives of Disease in Childhood 46(249): 728-729 (1971)

Familial hand abnormality and sensori-neural deafness: a new syndrome
, Journal of Pediatrics 78(1): 102-110 (1971)

Familial hearing disorder with a hearing pattern of low-and-middle-tone losses
, Jibi Inkoka Otolaryngology 40(4): 305-315 (1968)

Familial heart block
, Bollettino Della Societa Italiana di Cardiologia 19(1): 23-28 (1974)

Familial heart block and sinus bradycardia. Classification and natural history
, American Journal of Cardiology 29(4): 451-458 (1972)

Familial heart disease
, Diseases of the Chest 52(2): 153-158 (1967)

Familial hematuria and inner ear deafness (Alport's syndrome)
, Zeitschrift für Kinderheilkunde 94(1): 63-79 (1965)

Familial hematuria; clinico-pathological correlations
, Clinical Nephrology 17(4): 172-182 (1982)

Familial hematuric nephritis
, Pediatrics 38(5): 808-818 (1966)

Familial hematuric nephropathy
, Revista de la Facultad de Ciencias Medicas de Cordoba 28(2): 131-141 (1970)

Familial hematuric nephropathy with deafness (Alport's syndrome)
, Revista Clinica Espanola 125(4): 357-360 (1972)

Familial hematuric nephropathy with deafness (Alport's syndrome). Apropos of 2 series of cases
, Pediatrie 20(6): 649-664 (1965)

Familial hemifacial microsomia
, Cleft Palate Journal 20(1): 47-53 (1983)

Familial hemifacial microsomia due to autosomal dominant inheritance. Case reports
, Australian Dental Journal 39(5): 287-291 (1994)

Familial hemiplegic migraine associated with nystagmus
, Revue Neurologique 124(6): 526-530 (1971)

Familial hemiplegic migraine: EEG and CT scan study of two cases
, Annals of Neurology 10(4): 392-395 (1981)

Familial hemochromatoses
, La Revue de Medecine Interne 2(4): 367-368 (1981)

Familial hemochromatotic cardiomyopathy
, Medicina Clinica 80(11): 499-501 (1983)

Familial hemolytic anemia resulting from an abnormal red blood cell pyruvate kinase
, Journal of Laboratory and Clinical Medicine 72(3): 359-362 (1968)

Familial hemolytic anemia with inclusion bodies in the blood, bilifuscinuria and abnormal hemoglobin
, Revista Clinica Espanola 101(5): 367-368 (1966)

Familial hemolytic jaundice
, Chirurgia 22(11): 1005-1008 (1973)

Familial hemolytic-uremic syndrome associated with Coxsackie B infection
, Anales Espanoles de Pediatria 20(4): 369-374 (1984)

Familial hemophagocytic lymphohistiocytosis (FHLH) in Israel. I. Description of 11 patients of Iranian-Iraqi origin and review of the literature
, Cancer 54(10): 2109-2121 (1984)

Familial hemophagocytic reticulosis
, Verhandlungen der Deutschen Gesellschaft für Pathologie 58: 552 (1974)

Familial hemophagocytic reticulosis. A case report
, Monatsschrift für Kinderheilkunde 122(4): 164-168 (1974)

Familial hemophagocytic reticulosis. Cerebrospinal fluid cytology and neuropathological findings
, Journal of the Neurological Sciences 17(2): 193-207 (1972)

Familial hemorrhagic diathesis due to selective deficiency in platelet adhesiveness
, Sangre 12(3): 299-308 (1967)

Familial hepatic cirrhosis in infants associated with alpha1-antitrypsin SZ phenotype
, Journal of Pediatrics 85(2): 159-164 (1974)

Familial hepatitis B infection
, Zhonghua Yu Fang Yi Xue Za Zhi 14(4): 235-237 (1980)

Familial hepatocellular carcinoma and hepatitis B antigenemia in a New Zealand Chinese family
, Australian and New Zealand Journal of Medicine 13(3): 236-239 (1983)

Familial hepatocellular carcinoma in an endemic area of Thailand
, Cancer Genetics and Cytogenetics 11(1): 11-18 (1984)

Familial hepatoma with hepatitis-associated antigen
, Annals of Internal Medicine 74(3): 391-394 (1971)

Familial hereditary amyloidosis
, Folia Medica Neerlandica 10(1): 10-16 (1967)

Familial hereditary angioedema
, Alergia 30(1): 5-12 (1983)

Familial hereditary spherocytosis. Study in a rural zone of Baja California Sur
, Salud Publica de Mexico 25(3): 279-284 (1983)

Familial hereditary thrombocytopenia and HLA
, American Journal of Hematology 17(2): 113-116 (1984)

Familial herpes encephalitis
, Lancet 346(8989): 1553 (1995)

Familial histiocytic dermatoarthritis. A new syndrome
, American Journal of Medicine 54(6): 793-800 (1973)

Familial histiocytosis
, Lijecnicki Vjesnik 105(1): 22-25 (1983)

Familial histiocytosis in offspring of two pregnancies after artificial insemination
, New England Journal of Medicine 304(13): 757-759 (1981)

Familial history of congenital hydrocephalus
, British Medical Journal 289(6446): 696 (1984)

Familial holoprosencephaly with median cleft lip
, Journal de Genetique Humaine 21(3): 223-228 (1973)

Familial holotopistic striatal necrosis
, Acta Neuropathologica 13(3): 240-249 (1969)

Familial horseshoe kidney: a case report
, Journal of the Iowa Medical Society 63(8): 399-401 (1973)

Familial hyaline membrane disease. Morphologic and histochemical study of a case of bilateral polycystic kidney in a newborn infant
, Archivio "de Vecchi" Per l'Anatomia Patologica E la Medicina Clinica 49(1): 103-148 (1967)

Familial hydatidosis in Cyrenaica
, La Clinica Pediatrica 47(4): 280-287 (1965)

Familial hydrocephalus
, Birth Defects Original Article Series 7(1): 231 (1971)

Familial hydrocephalus, a hereditary disease
, Archives Francaises de Pediatrie 28(7): 787-788 (1971)

Familial hydrocephalus, recessive hereditary gonosomic disease (Bickers and Adams syndrome)
, Archives Francaises de Pediatrie 28(9): 971-974 (1971)

Familial hydronephrosis
, Zeitschrift für Kinderheilkunde 114(4): 313-321 (1973)

Familial hyper- and hypouricemias in random and hyperlipidemic recall cohorts: the Princeton School District Family Study
, Metabolism, Clinical and Experimental 32(3): 230-243 (1983)

Familial hyper-alpha-lipoproteinemia in 26 kindreds
, Clinical Genetics 17(1): 13-25 (1980)

Familial hyper-pre-betalipoproteinemia with observations on the metabolism of endogenous particles
, Journal of Laboratory and Clinical Medicine 76(1): 92-102 (1970)

Familial hyperaldosteronism, not suppressed by dexamethasone
, Journal of Clinical Endocrinology and Metabolism 55(5): 1013-1016 (1982)

Familial hyperargininemia
, Journal de Genetique Humaine 20(1): 69-84 (1972)

Familial hyperbetalipoproteinaemia
, Lancet 1(7761): 1171 (1972)

Familial hypercarotinaemia and hypovitaminosis A
, Proceedings of the Royal Society of Medicine 63(6): 605-606 (1970)

Familial hypercholesteremia and hypertension
, Beitrage Zur Pathologischen Anatomie und Zur Allgemeinen Pathologie 131(4): 450-481 (1965)

Familial hypercholesteremic tendinous xanthomatosis
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 74(6): 792-796 (1967)

Familial hypercholesterolaemia (familial hyper-beta-lipoproteinaemia or type II hyperlipoproteinaemia) in a Chinese family
, Singapore Medical Journal 14(2): 124-129 (1973)

Familial hypercholesterolaemia : effect of low density lipoproteins on cholesterol synthesis in lymphocytes from homozygous and heterozygous subjects
, Archives Internationales de Physiologie et de Biochimie 91(3): 179-185 (1983)

Familial hypercholesterolaemia and church affiliation
, Lancet 2(8255): 1120 (1981)

Familial hypercholesterolaemia and coronary disease in South Africa
, British Medical Journal 281(6244): 872 (1980)

Familial hypercholesterolaemia and primary hypothyroidism: coexistence of both disorders in a young woman with severe hypercholesterolaemia
, Clinical Endocrinology 14(2): 145-152 (1981)

Familial hypercholesterolaemia in an African family in Zimbabwe
, Central African Journal of Medicine 29(4): 75-77 (1983)

Familial hypercholesterolaemia in children
, Nursing Mirror and Midwives Journal 139(4): 74-76 (1974)

Familial hypercholesterolaemia--a common genetic disorder in the Afrikaans population
, South African Medical Journal 57(23): 943-947 (1980)

Familial hypercholesterolaemia: esterification of cholesterol in lymphocytes from homozygous and heterozygous subjects
, Archives Internationales de Physiologie et de Biochimie 92(5): 355-360 (1984)

Familial hypercholesterolaemic xanthomatosis and coronary heart disease in a ten-year-old girl
, Annales Paediatriae Fenniae 13(1): 35-38 (1967)

Familial hypercholesterolemia (one form of familial type II hyperlipoproteinemia). A study of its biochemical, genetic and clinical presentation in childhood
, Journal of Clinical Investigation 53(5): 1237-1249 (1974)

Familial hypercholesterolemia and coronary cardiopathy. Study of 2 families
, Acta Cardiologica 25(1): 69-76 (1970)

Familial hypercholesterolemia in a large indred. Evidence for a monogenic mechanism
, Annals of Internal Medicine 76(5): 711-720 (1972)

Familial hypercholesterolemia in children. A management program. Procedures for diagnosis and treatment in our pediatric departments
, Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 115(28): 3514 (1995)

Familial hypercholesterolemia proven by tissue culture and atherosclerosis in relation to other risk factors
, Agents and Actions. Supplements 16: 205-210 (1984)

Familial hypercholesterolemia with xanthoma tuberosum-multiplex. Discussion and case report
, International Surgery 49(3): 258-261 (1968)

Familial hypercholesterolemia. Evidence for a newly recognized mutation determining increased fibroblast receptor affinity but decreased capacity for low density lipoprotein in two siblings
, Journal of Clinical Investigation 70(4): 823-831 (1982)

Familial hypercholesterolemia. Problems of patients in dealing with their disease
, Mmw Munchener Medizinische Wochenschrift 124(38): 827-828 (1982)

Familial hypercholesterolemia. Screening, prevention and therapeutic possibilities
, Minerva Pediatrica 34(8): 325-336 (1982)

Familial hypercholesterolemia. Study of a family
, Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 36(3): 269-275 (1984)

Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity
, Proceedings of the National Academy of Sciences of the United States of America 71(3): 788-792 (1974)

Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol
, Proceedings of the National Academy of Sciences of the United States of America 70(10): 2804-2808 (1973)

Familial hypercholesterolemia: is causal therapy possible?
, Medizinische Monatsschrift für Pharmazeuten 5(2): 48-50 (1982)

Familial hypercholesterolemia: mechanism of inheritance
, Diabete and Metabolisme 6(3): 181-188 (1980)

Familial hypercholesterolemic cutaneo-tendineous xanthomatosis
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 76(6): 781-784 (1969)

Familial hypercholesterolemic cutaneotendinous xanthomatosis. Anatomo-clinical study. Apropos of 2 cases
, Annales d'Anatomie Pathologique 16(3): 233-250 (1971)

Familial hypercholesterolemic xanthomatosis. Apropos of 9 cases in the same family
, Lyon Medical 215(7): 385-402 (1966)

Familial hypercholesterolemic xanthomatosis: effect of colestipol on the lipoprotein profile
, La Nouvelle Presse Medicale 9(42): 3186 (1980)

Familial hyperchylomicronemia or Type I hyperlipoproteinemia
, Ugeskrift for Laeger 136(3): 125-129 (1974)

Familial hyperchylomicronemia. Enzymatic and physiologic studies
, American Journal of Medicine 50(4): 536-541 (1971)

Familial hypergammaglobulinemia in Waldenström's disease. Clinical case
, Giornale di Clinica Medica 63(4): 237-247 (1982)

Familial hyperglobulinaemic purpura in two young siblings. Clinical and immunobiologic studies
, Helvetica Paediatrica Acta 25(4): 421-427 (1970)

Familial hyperinsulinemia due to a structurally abnormal insulin. Definition of an emerging new clinical syndrome
, New England Journal of Medicine 310(20): 1288-1294 (1984)

Familial hyperkalaemia responsive to benzothiadiazine diuretic
, Lancet 1(8173): 879 (1980)

Familial hyperkalemic periodic paralysis
, Ugeskrift for Laeger 146(36): 2686-2688 (1984)

Familial hyperkeratosis lenticularis perstans associated with tumours of the skin
, British Journal of Dermatology 88(5): 453-458 (1973)

Familial hyperleucine-aminopeptidasemia--degrading ability of patient leucine-aminopeptidase to high molecular weight substrate
, Rinsho Byori. Japanese Journal of Clinical Pathology 33(11): 1301-1305 (1985)

Familial hyperlipemia
, Rinsho Byori. Japanese Journal of Clinical Pathology 18(4): 261-266 (1970)

Familial hyperlipidaemia and sea-blue histiocyte syndrome
, Sangre 27(2): 218-222 (1982)

Familial hyperlipidaemia with multiple xanthomatosis and euthyroid sick syndrome
, Indian Heart Journal 36(2): 124-126 (1984)

Familial hyperlipidaemia with xanthomas. Two case reports with review of literature
, Indian Journal of Dermatology 28(4): 177-181 (1983)

Familial hyperlipidaemias
, Proceedings of the Royal Society of Medicine 60(11 Part 1): 1147-1149 (1967)

Familial hyperlipidemia in coronary atherosclerotic heart disease
, Journal of the Association of Physicians of India 31(1): 15-19 (1983)

Familial hyperlipidemias. Diagnosis and treatment
, Archives of Dermatology 110(1): 43-50 (1974)

Familial hyperlipoproteinaemia and coronary heart disease
, Australian and New Zealand Journal of Medicine 4(1): 91-92 (1974)

Familial hyperlipoproteinaemia and the exocrine pancreas
, Review of Czechoslovak Medicine 19(4): 230-237 (1973)

Familial hyperlipoproteinaemia. A study of 152 members of 26 families
, Danish Medical Bulletin 18(4): 100-104 (1971)

Familial hyperlipoproteinemia
, Saishin Igaku. Modern Medicine 27(3): 498-503 (1972)

Familial hyperlipoproteinemia and exocrine pancreas
, Scandinavian Journal of Gastroenterology 6(2): 139-143 (1971)

Familial hyperlipoproteinemia and its treatment
, Polski Tygodnik Lekarski 28(23): 857-860 (1973)

Familial hyperlipoproteinemia type 3
, Archives of Dermatology 100(4): 401-406 (1969)

Familial hyperlipoproteinemic syndromes
, University of Michigan Medical Center Journal 32(6): 277-282 (1966)

Familial hyperlysinemia with lysine-ketoglutarate reductase insufficiency
, Journal of Clinical Investigation 48(8): 1447-1452 (1969)

Familial hyperostosis of obscure nature
, Metabolism, Clinical and Experimental 20(10): 910-926 (1971)

Familial hyperparathyroidism (report of three cases)
, West Virginia Medical Journal 66(1): 1-4 (1970)

Familial hyperparathyroidism caused by solitary adenomas
, Surgery 92(3): 486-490 (1982)

Familial hyperparathyroidism with malignant gastrin-producing duodenal tumor--MEN type I
, Horumon to Rinsho. Clinical Endocrinology 31(Suppl): 156-158 (1983)

Familial hyperparathyroidism. Mild hypercalcemia in at least nine members of a kindred
, Annals of Internal Medicine 78(3): 371-377 (1973)

Familial hyperphosphatase with mental retardation, seizures, and neurologic deficits
, Journal of Pediatrics 77(1): 74-85 (1970)

Familial hyperphosphatasemia with ateliosis and hypermetabolism of growing membranous bone; review of the clinical, radiographic and chemical features
, Bulletin of the Hospital for Joint Diseases 33(2): 81-110 (1972)

Familial hyperprebetalipoproteinemia
, Polski Tygodnik Lekarski 35(14): 501-502 (1980)

Familial hyperproinsulinemia. Two cohorts secreting indistinguishable type II intermediates of proinsulin conversion
, Journal of Clinical Investigation 73(3): 714-719 (1984)

Familial hyperprolinemia
, Neuropsihijatrija 16(1): 15-23 (1968)

Familial hyperprolinemia with nephropathy
, Revista Clinica Espanola 118(2): 141-150 (1970)

Familial hyperprolinemia without mental retardation and hereditary nephropathy
, Monographs in Human Genetics 6: 144-145 (1972)

Familial hyperprolinemia--a case in a family
, Polskie Archiwum Medycyny Wewnetrznej 51(2): 189-197 (1974)

Familial hypersensitivity pneumonitis induced by Bacillus subtilis
, American Review of Respiratory Disease 122(2): 339-348 (1980)

Familial hypersensitivity to insect stings
, Lancet 2(7722): 496 (1971)

Familial hypertension and horseshoe kidney
, Acta Isotopica 9(2): 247-252 (1968)

Familial hyperthecosis: comparison of endocrinologic and histologic findings with polycystic ovarian disease
, American Journal of Obstetrics and Gynecology 117(7): 976-982 (1973)

Familial hyperthyreosis
, Schweizerische Medizinische Wochenschrift 96(22): 727-728 (1966)

Familial hyperthyroidism and cochlear hearing loss syndrome with manifestation at a young age
, Ceskoslovenska Otolaryngologie 32(1): 34-39 (1983)

Familial hyperthyroidism due to inappropriate thyrotropin secretion successfully treated with triiodothyronine
, Journal of Clinical Endocrinology and Metabolism 54(1): 76-82 (1982)

Familial hyperthyroidism including two siblings with neonatal Graves' disease
, Journal of Pediatrics 78(4): 625-632 (1971)

Familial hyperthyroidism without evidence of autoimmunity
, Acta Endocrinologica 100(4): 512-518 (1982)

Familial hyperthyroxinemia due to abnormal thyroid hormone binding
, Annals of Internal Medicine 96(2): 183-186 (1982)

Familial hypertonic fever during anesthesia
, Surgical Clinics of North America 50(2): 433-437 (1970)

Familial hypertrichosis cubiti: hairy elbows syndrome
, Journal of Medical Genetics 7(2): 158-160 (1970)

Familial hypertriglyceridemia and the regulation of lipid synthesis by insulin and triiodothyronine in human cell cultures
, Agents and Actions. Supplements 16: 211-216 (1984)

Familial hypertriglyceridemia. Genetics and pathogeny
, Revista Clinica Espanola 169(2): 109-112 (1983)

Familial hypertrophic cardiomyopathy and preexcitation
, American Heart Journal 107(1): 176-179 (1984)

Familial hypertrophic cardiomyopathy in Ceylon
, British Heart Journal 35(2): 181-188 (1973)

Familial hypertrophic cardiomyopathy. Nonsense versus missense mutations
, Circulation 91(12): 2865-2867 (1995)

Familial hypertrophic cardiomyopathy: vectorcardiographic findings in echocardiographically unaffected relative
, British Heart Journal 47(6): 588-595 (1982)

Familial hypertrophic osteoarthropathy (pachydermo periostosis) with eunuchoidism
, New Zealand Medical Journal 65(408): 528-532 (1966)

Familial hypertrophic subaortic stenosis
, Bollettino Della Societa Italiana di Cardiologia 11(4): 1322-1333 (1966)

Familial hypertryptophanemia, tryptophanuria and indoleketonuria
, Clinica Chimica Acta; International Journal of Clinical Chemistry 131(3): 247-256 (1983)

Familial hyperuricaemia and hypertriglyceridaemia
, Annals of the Rheumatic Diseases 32(6): 497-500 (1973)

Familial hyperuricemia and renal disease
, Archives of Internal Medicine 140(5): 680-684 (1980)

Familial hyperuricemic nephropathy
, American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 25(2): 235-241 (1995)

Familial hypo- -lipoproteinaemia
, Journal of the Neurological Sciences 16(1): 93-101 (1972)

Familial hypo-alpha-lipoproteinemia
, Clinica Chimica Acta; International Journal of Clinical Chemistry 114(1): 45-52 (1981)

Familial hypo-beta-lipoproteinemia: a genetic disorder of lipid metabolism with nervous system involvement
, American Journal of Medicine 46(6): 886-900 (1969)

Familial hypoalphalipoproteinemia. Vergani's disease
, Minerva Medica 74(44): 2659-2664 (1983)

Familial hypobetalipoproteinaemia
, Archives of Disease in Childhood 47(254): 671 (1972)

Familial hypobetalipoproteinemia: report of a case with psychomotor retardation
, Pediatrics 54(1): 111-113 (1974)

Familial hypocalciuric hypercalcaemia and acute pancreatitis
, British Medical Journal 282(6269): 1023-1025 (1981)

Familial hypocalciuric hypercalcaemia: association with neonatal primary hyperparathyroidism, and possible linkage with HLA haplotype
, Clinical Endocrinology 21(1): 57-64 (1984)

Familial hypocalciuric hypercalcemia involving four members of a kindred including a girl with severe neonatal primary hyperparathyroidism
, Mineral and Electrolyte Metabolism 9(1): 51-54 (1983)

Familial hypocalciuric hypercalcemia syndrome
, La Nouvelle Presse Medicale 11(43): 3205 (1982)

Familial hypocalciuric hypercalcemia with severe neonatal primary hyperparathyroidism
, Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 71(4): 479-484 (1982)

Familial hypocalciuric hypercalcemia. A new family
, Revue du Rhumatisme et des Maladies Osteo-Articulaires 52(11): 609-612 (1985)

Familial hypocalciuric hypercalcemia. Report of a new family
, Journal of Endocrinological Investigation 5(2): 125-127 (1982)

Familial hypocalciuric hypercalcemia: recognition among patients referred after unsuccessful parathyroid exploration
, Annals of Internal Medicine 92(3): 351-356 (1980)

Familial hypocalciuric hypercalcemia: the relation to primary parathyroid hyperplasia
, New England Journal of Medicine 307(7): 416-426 (1982)

Familial hypocalciuric hypercalcemia: two case reports
, Annales de Medecine Interne 133(4): 281-284 (1982)

Familial hypocalciuric hypocalcemia
, New England Journal of Medicine 308(1): 48-49 (1983)

Familial hypochromic hypersideremic (sidero-achrestic) anemia
, Annales Paediatrici. International Review of Pediatrics 206(2): 97-119 (1966)

Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3,B7 haplotype
, JAMA 245(6): 602-604 (1981)

Familial hypodontia in the permanent dentition: a case report
, Journal of Dentistry 9(3): 260-264 (1981)

Familial hypogammaglobulinemia with special reference to hypogammaM-globulinemia
, Praxis 55(27): 759-764 (1966)

Familial hypogammaglobulinemia with variable serum immunoglobulins. Concordance with lymphocyte ecto-5'-nucleotidase deficiency
, American Journal of Diseases of Children 135(9): 795-798 (1981)

Familial hypogammaglobulinemia-A
, Annals of Allergy 27(8): 393-402 (1969)

Familial hypogammaglobulinemia. Diagnosis and specific therapy
, Munchener Medizinische Wochenschrift 113(10): 339-344 (1971)

Familial hypogammaglobulinemia. Genetic linkage with alpha 1-antitrypsin deficiency
, Archives of Internal Medicine 143(3): 575-577 (1983)

Familial hypogonadism
, Vutreshni Bolesti 11(5): 127-129 (1972)

Familial hypogonadism with a balanced reciprocal 1;12 translocation
, Journal of Medical Genetics 20(6): 478 (1983)

Familial hypogonadism with anosmia: Kallmann Syndrome
, Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 131(4): 232-234 (1983)

Familial hypogonadotropic hypogonadism with anosmia
, Archives of Internal Medicine 121(6): 534-538 (1968)

Familial hypokalaemic periodic paralysis
, Lancet 1(8230): 1140-1141 (1981)

Familial hypokalemia associated with renal interstitial fibrosis
, American Journal of Medicine 57(6): 971-977 (1974)

Familial hypokalemia or myopathy?
, Mmw Munchener Medizinische Wochenschrift 122(1): 25 (1980)

Familial hypokalemic paralysis: a case study
, Rivista di Patologia Nervosa E Mentale 105(3): 113-118 (1984)

Familial hypokalemic periodic paralysis with permanent myopathy. A clinical and ultrastructural study
, Journal of Neuropathology and Experimental Neurology 26(1): 98-114 (1967)

Familial hypomagnesemia in a girl
, Pediatria Polska 55(9): 1083-1086 (1980)

Familial hypomagnesemia--a follow-up examination of three patients after 9 to 12 years of treatment
, Pediatric Research 15(8): 1134-1139 (1981)

Familial hypomagnesemia. Biochemical, histological and hereditary aspects studied in two brothers
, Acta Paediatrica Scandinavica 58(5): 433-444 (1969)

Familial hypoparathyroidism
, Medizinische Klinik 69(49): 2029-2032 (1974)

Familial hypoparathyroidism syndrome with hypercalciuria
, Annales de Pediatrie 15(4): 1045-1060 (1968)

Familial hypoparathyroidism. Case reports and a eview of the literature
, Neurology 18(1 Pt 1): 75-80 (1968)

Familial hypophosphatasemia
, Deutsche Medizinische Wochenschrift 120(8): 271 (1995)

Familial hypophosphatemia and vitamin-resistant rickets. Biochemical and genetic aspects
, L'Union Medicale du Canada 99(12): 2209-2214 (1970)

Familial hypophosphatemia in 3 females of 3 consecutive generations
, Minerva Ortopedica 19(1): 59-62 (1968)

Familial hypophosphatemia: the dilemma of treatment
, New England Journal of Medicine 289(10): 531-532 (1973)

Familial hypophosphatemic resistent rachitism
, Revista Chilena de Pediatria 42(7): 483-489 (1971)

Familial hypophosphatemic rickets showing autosomal dominant inheritance
, Birth Defects Original Article Series 7(6): 287-295 (1971)

Familial hypophosphatemic vitamin D resistant rickets. The neonatal period and infancy
, Acta Paediatrica Scandinavica 58(3): 213-219 (1969)

Familial hypophosphoremic rickets: pathogenic considerations based on two cases
, Medicina Clinica 74(7): 271-274 (1980)

Familial hypophyseal dwarfism
, Schweizerische Medizinische Wochenschrift 98(19): 705-709 (1968)

Familial hypopituitarism
, Monatsschrift für Kinderheilkunde 118(8): 470-473 (1970)

Familial hypoplasia of both internal carotid arteries
, Archives of Neurology 24(1): 1-10 (1971)

Familial hypoplasia of the iris stroma associated with glaucoma
, British Journal of Ophthalmology 53(7): 433-438 (1969)

Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome)--report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings
, Rhode Island Medical Journal 49(2): 103-110 (1966)

Familial hypoplastic glomerulocystic kidney. A new entity?
, Clinical Nephrology 18(5): 263-268 (1982)

Familial hypoplastic leukemia in brothers
, Japanese Journal of Clinical Hematology 24(7): 874-880 (1983)

Familial hypospadias in three generations
, International Urology and Nephrology 12(3): 217-220 (1980)

Familial hypothyreodism with increased butanol-inextractable plasma iodine
, Srpski Arhiv Za Celokupno Lekarstvo 95(6): 603-609 (1967)

Familial hypothyroidism
, Voprosy Okhrany Materinstva i Detstva 13(6): 81-83 (1968)

Familial hypothyroidism with deafness (Pendred's syndrome)
, Endokrynologia Polska 24(3): 257-264 (1973)

Familial idiopathic basal ganglia calcification exhibiting "dystonia musculorum deformans" features
, European Neurology 12(5-6): 351-359 (1974)

Familial idiopathic cardiomyopathy
, Vutreshni Bolesti 21(4): 96-99 (1982)

Familial idiopathic generalized root resorption
, Tandlaegebladet 88(14): 475-479 (1984)

Familial idiopathic gingival hyperplasia with keloid formation and ectodermal dysplasia
, Dental Student 45(8): 683-685 (1967)

Familial idiopathic gonadotropin deficiency: a hypothalamic form of hypogonadism
, American Journal of Medical Genetics 15(3): 405-416 (1983)

Familial idiopathic hyperlipemis: diagnostic and therapeutic considerations
, Pediatria 23(1): 73-78 (1974)

Familial idiopathic hypertrophic osteoarthropathy and cranial suture defects in children
, Skeletal Radiology 8(2): 105-109 (1982)

Familial idiopathic hypertrophic osteoarthropathy in a 2-year-old girl
, Wiadomosci Lekarskie 34(2): 149-152 (1981)

Familial idiopathic hypoparathyroidism associated with progressive sensorineural deafness(1)
, Nihon Naibunpi Gakkai Zasshi 59(3): 241-247 (1983)

Familial idiopathic membranous glomerulonephritis
, International Journal of Pediatric Nephrology 5(4): 193-196 (1984)

Familial idiopathic osteoarthropathy of children: a case report and progress
, British Journal of Radiology 43(512): 568-570 (1970)

Familial idiopathic priapism: a case report
, Journal of Urology 131(3): 542-543 (1984)

Familial idiopathic thrombocytopenic purpura
, Annales de Pediatrie 28(3): 215-220 (1981)

Familial idiopathic thrombocytopenic purpura. Raynaud's phenomenon
, Proceedings of the Royal Society of Medicine 62(12): 1277-1278 (1969)

Familial immunoglobulin anomalies in paraproteinemic diseases
, Minerva Medica 63(22): 1257-1273 (1972)

Familial imperforate anus: Report of a family
, Diseases of the Colon and Rectum 17(4): 562-564 (1974)

Familial inappropriate TSH secretion: evidence suggesting a dissociated pituitary resistance to T3 and T4
, Journal of Endocrinological Investigation 4(4): 413-422 (1981)

Familial incidence and degenerative vascular cerebral lesions of advanced age. (Comparative anatomical and histologic study of 64 brains from 30 family groups)
, L'Encephale 54(3): 204-239 (1965)

Familial incidence and modes of inheritance of hypertrophic cardiomyopathy. Genetic analysis of several families
, Cardiologia 28(4): 337-342 (1983)

Familial incidence in two cases of aneurysmal bone cyst
, Italian Journal of Orthopaedics and Traumatology 7(2): 251-253 (1981)

Familial incidence of Alzheimer's cortical neurofibrillar changes
, Psychiatria et Neurologia 150(4): 235-247 (1965)

Familial incidence of Crohn disease
, Fortschritte der Medizin 99(10): 340-341 (1981)

Familial incidence of Down's disease
, Ceskoslovenska Pediatrie 28(2): 81-83 (1973)

Familial incidence of Gilles de la Tourette's disease, with observations on aetiology and treatment
, British Journal of Psychiatry: the Journal of Mental Science 122(571): 655-658 (1973)

Familial incidence of Hodgkin's disease
, Archivio "e. Maragliano" di Patologia E Clinica 23(3): 391-394 (1967)

Familial incidence of Leptospira canicola infections and Weil's disease and diagnostic difficulties in differentiation from Heine-Medina disease
, Wiadomosci Lekarskie 20(8): 737-739 (1967)

Familial incidence of Pasteurella pseudotuberculosis infection
, Orvosi Hetilap 114(21): 1248-1250 (1973)

Familial incidence of atrial septal defect. A report of four siblings and review of the literature
, Chest 65(1): 56-58 (1974)

Familial incidence of benign recurrent intrahepatic cholestasis
, Orvosi Hetilap 121(45): 2771-2774 (1980)

Familial incidence of bifid and double ureters
, Archives of Disease in Childhood 49(5): 390-393 (1974)

Familial incidence of bilateral anorchia. Study of three siblings
, Medicina Clinica 75(7): 292-295 (1980)

Familial incidence of bird-breeder's lung and HLA
, Medicina Clinica 76(5): 221-222 (1981)

Familial incidence of bronchiectasis and alpha-1 antitrypsin deficiency
, Schweizerische Medizinische Wochenschrift 104(48): 1705-1711 (1974)

Familial incidence of carcinoma of the kidney in patients with von Hippel-Lindau disease
, Bratislavske Lekarske Listy 81(4): 465-471 (1984)

Familial incidence of cerebral aneurysms
, British Medical Journal 1(5480): 147-148 (1966)

Familial incidence of cerebral palsy
, Developmental Medicine and Child Neurology 10(2): 250 (1968)

Familial incidence of cerebrovascular disease
, Journal of Medical Genetics 8(1): 84-89 (1971)

Familial incidence of certain congenital urinary anomalies
, Revista Venezolana de Urologia 17(3): 321-326 (1965)

Familial incidence of congenital alopecia and hypotrichosis
, Ceskoslovenska Dermatologie 55(3): 196-201 (1980)

Familial incidence of congenital anorectal anomalies
, Journal of Pediatric Surgery 19(2): 179-182 (1984)

Familial incidence of congenital choanal atresia
, Zeitschrift für Laryngologie Rhinologie Otologie und ihre Grenzgebiete 45(2): 67-73 (1966)

Familial incidence of congenital heart defects
, Munchener Medizinische Wochenschrift 109(2): 86-90 (1967)

Familial incidence of congenital hepatic fibrosis
, Casopis Lekaru Ceskych 120(41): 1258-1261 (1981)

Familial incidence of double malignancies
, Schweizerische Medizinische Wochenschrift 96(7): 218-219 (1966)

Familial incidence of favus in 3 generations
, Ceskoslovenska Dermatologie 48(2): 103-107 (1973)

Familial incidence of fructose intolerance
, Orvosi Hetilap 107(40): 1893-1895 (1966 )

Familial incidence of granular corneal dystrophy
, Ceskoslovenska Oftalmologie 39(4): 240-243 (1983)

Familial incidence of infantile arterial calcification
, Ceskoslovenska Pediatrie 38(11): 658-661 (1983)

Familial incidence of intestinal carcinoma
, Schweizerische Medizinische Wochenschrift 102(46): 1687-1692 (1972)

Familial incidence of intracranial aneurysms
, Arquivos de Neuro-Psiquiatria 31(3): 171-179 (1973)

Familial incidence of isolated TSH deficiency
, Nihon Rinsho. Japanese Journal of Clinical Medicine 32(7): 2411-2413 (1974)

Familial incidence of juvenile diabets mellitus, progressive optic atrophy, and neurogenic deafness
, British Journal of Ophthalmology 56(6): 496-500 (1972)

Familial incidence of juvenile polyposis coli
, Surgery Gynecology and Obstetrics 138(2): 185-188 (1974)

Familial incidence of kidney cysts with liver cirrhosis, portal hypertension and hypersplenism (including chromosome analysis)
, Zeitschrift für Urologie und Nephrologie 65(9): 679-682 (1972)

Familial incidence of malignant melanoma
, Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 89(24): 1900-1902 (1969)

Familial incidence of osseous lesions in neurofibromatosis
, Journal of the Indian Medical Association 74(5): 93-94 (1980)

Familial incidence of osteogenesis imperfecta: seven cases in two families
, Indian Pediatrics 2(12): 442-445 (1965)

Familial incidence of ovarian dermoid cysts
, Canadian Medical Association Journal 108(7): 892-893 (1973)

Familial incidence of peptic ulcer
, Polski Tygodnik Lekarski 20(21): 769-770 (1965)

Familial incidence of pericentric inversion of X chromosome
, Ceskoslovenska Pediatrie 29(5): 245-247 (1974)

Familial incidence of post-streptococcal glomerulonephritis
, Boletin Medico del Hospital Infantil de Mexico 38(1): 119-129 (1981)

Familial incidence of psoriasis
, Giornale Italiano di Dermatolotia. Minerva Dermatologica 46(12): 543-544 (1971)

Familial incidence of renal malformations
, Wiadomosci Lekarskie 24(22): 2087-2090 (1971)

Familial incidence of reticular corneal dystrophy
, Ceskoslovenska Oftalmologie 39(4): 235-239 (1983)

Familial incidence of sarcoidosis
, Ugeskrift for Laeger 131(10): 413-416 (1969)

Familial incidence of the Bloch-Sulzberger syndrome (Incontinentia pigmenti) with ocular involvement
, Klinische Monatsblatter für Augenheilkunde 157(5): 652-663 (1970)

Familial incidence of the Morris syndrome
, Attualita di Ostetricia E Ginecologia 15(2): 109-119 (1969)

Familial incidence of thyroid functional changes in patients with gonadal dysgenesis
, Studii Si Cercetari de Endocrinologie 22(3): 203-214 (1971)

Familial incidence of "ecto-mesodermal dysplasia" (Ellis-van Creveld syndrome). Study of the syndrome in 3 brothers
, Minerva Pediatrica 17(25): 1322-1330 (1965)

Familial incidences of adult T-cell leukemia-lymphoma--with special reference to recent observations on 2 families
, Japanese Journal of Clinical Hematology 23(4): 464-471 (1982)

Familial incidences of hemangioblastoma of the cerebellum
, No Shinkei Geka. Neurological Surgery 11(5): 549-555 (1983)

Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias
, New England Journal of Medicine 291(18): 944-949 (1974)

Familial inducible torsade de pointes with normal QT interval
, European Heart Journal 4(6): 383-390 (1983)

Familial infantile amaurotic idiocy with visceral involvement
, Annales de Pediatrie 14(6): 457-465 (1967)

Familial infantile cortical hyperostosis with prenatal beginning
, Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 105(2): 154-163 (1966)

Familial infantile cortical hyperostosis: an update
, Ajr. American Journal of Roentgenology 137(1): 93-96 (1981)

Familial infantile dementia: clinical study of 4 young siblings
, L'Ospedale Psichiatrico 38(4): 508-523 (1970)

Familial infantile olivopontocerebellar atrophy
, Pediatric Neurology 13(1): 14-18 (1995)

Familial infantile osteochondrosis deformans tibiae. Idiopathic tibia vara. A case report
, Acta Orthopaedica Scandinavica 38(1): 81-87 (1967)

Familial infantile pigmentary cirrhosis. Apropos of a case
, La Presse Medicale 75(9): 451-456 (1967)

Familial infantile splenomegalic hepatic cirrhosis. Study of 2 cases
, Archivio Italiano Delle Malattie Dell'apparato Digerente 33(1): 73-104 (1966)

Familial infection by Yersinia enterocolitica
, Acta Clinica Belgica 21(3): 206-215 (1966)

Familial infection routes of fungi in the fields of obstetrics and gynecology
, Nihon Sanka Fujinka Gakkai Zasshi 23(6): 501-508 (1971)

Familial infection with T. vaginalis
, Wiadomosci Parazytologiczne 19(3): 335-336 (1973)

Familial infections with candida
, Dermatologische Monatschrift 159(4): 410-411 (1973)

Familial influences in childhood depression
, Pediatric Annals 13(1): 32-36 (1984)

Familial infra-diaphragmatic total abnormal pulmonary venous return
, Archives Francaises de Pediatrie 25(10): 1141-1149 (1968)

Familial infradiaphragmatic total anomalous pulmonary venous return
, Pediatrie 36(6): 463-468 (1981)

Familial insensitivity of the pituitary and periphery to thyroid hormone: a case report in two generations and a review of the literature
, Metabolism, Clinical and Experimental 31(5): 510-513 (1982)

Familial insertional translocation
, Lancet 2(7770): 231 (1972)

Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1 leads to q24 in different offspring
, American Journal of Medical Genetics 9(2): 105-111 (1981)

Familial insulin-resistant diabetes secondary to an affinity defect of the insulin receptor
, Human Genetics 64(4): 407-411 (1983)

Familial intention tremor, ataxia, and lipofuscinosis. Liver biopsy studies
, Neurology 19(5): 503-509 (1969)

Familial interactions of male rhesus monkeys in a semi-free-ranging troop
, American Journal of Physical Anthropology 38(2): 605-611 (1973)

Familial interatrial communication and long PR
, Medicina Clinica 80(19): 862-863 (1983)

Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and a response to acetazolamide
, Journal of the Neurological Sciences 64(1): 89-97 (1984)

Familial intermittent diplopia: a report of two cases
, Aviation Space and Environmental Medicine 53(7): 704-707 (1982)

Familial interrelational approach in psychiatry: a "philosophy" rather than a technic
, Acta Psychiatrica Belgica 74(4): 389-404 (1974)

Familial interstitial calcinosis (a 20-year follow-up study)
, Zeitschrift für Orthopadie und ihre Grenzgebiete 120(6): 774-779 (1982)

Familial interstitial pulmonary fibrosis
, Prensa Medica Argentina 58(10): 495-500 (1971)

Familial intra-areolar polythelia with mammary hypoplasia
, Scandinavian Journal of Plastic and Reconstructive Surgery 16(3): 287-291 (1982)

Familial intracranial aneurysm
, International Surgery 58(7): 508 (1973)

Familial intracranial aneurysm and infundibular widening
, Neuroradiology 25(5): 329-334 (1983)

Familial intracranial aneurysms and otosclerosis
, Rivista di Neurologia 43(3): 229-235 (1973)

Familial intracranial aneurysms, with two occurring at the distal anterior cerebral artery
, Neurosurgery 12(2): 214-216 (1983)

Familial intracranial aneurysms. Case report
, Journal of Neurosurgery 57(3): 416-417 (1982)

Familial intracranial aneurysms. Review of literature and presentation of six new cases
, Acta Neurochirurgica 30(1-2): 129-137 (1974)

Familial intracranial aneurysms. Six cases among 13 siblings
, Journal of Neurosurgery 52(4): 501-503 (1980)

Familial intracranial aneurysms: report of four families
, Surgical Neurology 19(3): 260-262 (1983)

Familial intracranial gliomas
, Surgical Neurology 22(1): 76-78 (1984)

Familial intrahepatic cholestasis with mental and growth retardation
, Pediatrics 38(5): 819-836 (1966)

Familial intrahepatic cholestatic jaundice in infancy
, Archives of Disease in Childhood 41(217): 320-328 (1966)

Familial intrahepatic obstructive jaundice--a case of jaundice as a new independent entity
, Nihon Shonika Gakkai Zasshi. Acta Paediatrica Japonica 71(12): 1469-1477 (1967)

Familial intraocular melanoma
, Transactions - American Academy of Ophthalmology and Otolaryngology. American Academy of Ophthalmology and Otolaryngology 74(5): 955-958 (1970)

Familial intraventricular papilloma. Angiographic characteristics
, Neuro-Chirurgie 11(3): 267-272 (1965)

Familial intrinsic hypothyroidism (2 brothers) and induced gout crisis caused by opotherapy
, Revista Clinica Espanola 119(5): 451-454 (1970)

Familial inv(1) (p3500q21.3) associated with azoospermia
, Human Genetics 66(2-3): 165-167 (1984)

Familial inversion translocation (8;13) with partial trisomy 13 in several family members
, European Journal of Pediatrics 140(2): 105-108 (1983)

Familial investigation of the 4-5 c-sec variation of the basic rhythm
, Electroencephalography and Clinical Neurophysiology 26(4): 445 (1969)

Familial investigations in persons with obesity
, Folia Medica 24(3): 36-39 (1982)

Familial irido-crystalline abnormalities
, Annales d'Oculistique 205(3): 291-294 (1972)

Familial iridoschisis complicated with cornea guttata
, Ophthalmologica. Journal International d'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift für Augenheilkunde 169(6): 411-415 (1974)

Familial isolated growth hormone deficiency
, Naika. Internal Medicine 23(3): 580-584 (1969)

Familial isolated primary hyperparathyroidism
, Clinical Endocrinology 42(4): 441-443 (1995)

Familial jaundice caused by intrahepatic cholestasis
, Deutsche Zeitschrift für Verdauungs- und Stoffwechselkrankheiten 26(1): 23-31 (1966)

Familial jaw cysts in Charcot-Marie-Tooth disease
, Journal of Medical Genetics 6(2): 193-195 (1969)

Familial jejunal atresia with 'apple-peel' variant
, Journal of the Royal Society of Medicine 74(7): 499-501 (1981)

Familial jejunal atresia: three cases in one family
, Journal of Pediatrics 73(5): 753-755 (1968)

Familial joint chondrocalcinosis (pseudogout syndrome)
, Folia Medica Neerlandica 9(2): 48-53 (1966)

Familial joint instability syndrome
, American Journal of Medical Genetics 6(3): 221-228 (1980)

Familial juvenile acromegalic syndrome accompanied by abnormal somatotropin metabolism
, Folia Endocrinologica 23(3): 241-251 (1970)

Familial juvenile amyotropic lateral sclerosis
, Indian Pediatrics 5(3): 119-121 (1968)

Familial juvenile cirrhosis
, Prensa Medica Argentina 53(37): 2005-2009 (1966)

Familial juvenile elastoma
, Australasian Journal of Dermatology 35(2): 87-90 (1994)

Familial juvenile elastoma: osteopoikilosis (2 cases)
, Proceedings of the Royal Society of Medicine 60(12): 1267 (1967)

Familial juvenile glaucoma
, Oftalmologicheskii Zhurnal 29(7): 552 (1974)

Familial juvenile glio-neural dystrophy. Acutely beginning progressive encephalopathy with right-side occipitol-parietal focal symptoms and status epilepticus
, Archiv für Psychiatrie und Nervenkrankheiten 212(4): 400-422 (1969)

Familial juvenile gout caused by partial HGPRT deficiency with neurologic manifestations; a variant of the Lesch-Nyhan syndrome?
, Bulletin et Memoires de l'Academie Royale de Medecine de Belgique 135(3): 219-231 (1980)

Familial juvenile hyperuricaemic nephropathy in adolescents
, Advances in Experimental Medicine and Biology 370: 73-76 (1994)

Familial juvenile liver cirrhosis in 3 sisters. Clinical, biopsy and autopsy studies
, Acta Hepato-Splenologica 15(4): 209-218 (1968)

Familial juvenile nephronophthisis (report of 5 cases)
, Rivista di Clinica Pediatrica 81(5): 779-791 (1968)

Familial juvenile nephronophthisis and medullary cystic disease
, Journal of Pediatrics 73(1): 77-83 (1968)

Familial juvenile nephronophthisis with hepatic fibrosis and neurocutaneous dysplasia
, Helvetica Paediatrica Acta 35(3): 261-267 (1980)

Familial juvenile nephronophthisis--report of cases in two siblings
, Acta Paediatrica Japonica: Overseas Edition 9(17): 1-6 (1967)

Familial juvenile nephronophthisis. Experience with eleven cases
, Birth Defects Original Article Series 10(4): 32-34 (1974)

Familial juvenile nephronophthisis. Report of cases in two siblings
, Klinische Padiatrie 184(3): 213-219 (1972)

Familial juvenile periodontosis associated with keratodermia palmaris et plantaris (Papillon-Lefévre syndrome)
, Rassegna Internazionale di Stomatologia Pratica 23(4): 111-124 (1972)

Familial juvenile polyposis coli; increased risk of colorectal cancer
, Gut 25(7): 792-800 (1984)

Familial juvenile polyposis of the stomach and large intestine
, Rinsho Hoshasen. Clinical Radiography 25(13): 1389-1395 (1980)

Familial juvenile polyposis: patterns of recurrence and implications for surgical management
, Journal of the American College of Surgeons 181(5): 407-413 (1995)

Familial juvenile type III spinal cord arteriovenous malformation: urodynamic findings
, Journal of Urology 130(5): 946-947 (1983)

Familial keratosis punctata palmaris et plantaris associated with multiple lipomas
, Medicina Clinica 83(16): 692 (1984)

Familial kidney cancer and the HLA system. 4 cases of cancer of the left kidney in a sibship
, La Nouvelle Presse Medicale 3(24): 1539-1542 (1974)

Familial laryngeal abductor paralysis and psychomotor retardation
, Clinical Genetics 4(5): 429-433 (1973)

Familial laryngeal abductor paralysis with presumed autosomal dominant inheritance
, Annals of Otology Rhinology and Laryngology 91(3 Pt 1): 323-324 (1982)

Familial late complement component (C6, C7) deficiency with chronic meningococcemia
, Archives of Internal Medicine 140(7): 929-933 (1980)

Familial late onset oculopharyngeal muscular dystrophy
, Postgraduate Medical Journal 57(663): 41-43 (1981)

Familial lead poisoning from contaminated wine
, Italian Journal of Neurological Sciences 2(3): 283-290 (1981)

Familial lecithin cholesterol acyltransferase deficiencies
, Nihon Rinsho. Japanese Journal of Clinical Medicine 41(8): 1832-1837 (1983)

Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: evidence for functionally defective enzyme in homozygotes and obligate heterozygotes
, Human Genetics 62(1): 82-85 (1982)

Familial lecithin-cholesterol acyltransferase: identification of heterozygotes with half-normal enzyme activity and mass
, Human Genetics 58(3): 306-309 (1981)

Familial lecithin-cholesterol-acyltransferase-deficiency
, Ugeskrift for Laeger 136(4): 206 (1974)

Familial lecithin: cholesterol acyltransferase deficiency. Study of two new patients and their close relatives
, Acta Medica Scandinavica 188(4): 323-326 (1970)

Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement
, Advances in Nephrology from the Necker Hospital 10: 167-185 (1981)

Familial lecithin:cholesterol acyltransferase deficiency--a clinical survey
, Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum 137: 73-82 (1974)

Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members
, Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum 137: 101-105 (1974)

Familial lecithin:cholesterol acyltransferase deficiency. Studies on lipid composition and morphology of tissues
, Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum 137: 93-100 (1974)

Familial lecithin:cholesterol acyltransferase deficiency. Ultrastructural studies on lipid deposition and tissue reactions
, Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum 137: 135-146 (1974)

Familial left anterior hemiblock
, Bollettino Della Societa Italiana di Cardiologia 19(1): 29-38 (1974)

Familial leukaemia
, Acta Haematologica 48(2): 98-103 (1972)

Familial leukaemia with coincident malignant disease
, Ceylon Medical Journal 26(3): 125-128 (1981)

Familial leukemia (chronic and acute) in 2 successive generations
, Sangre 12(3): 331-332 (1967)

Familial leukemia or a new syndrome?
, Pediatria Polska 46(4): 495-502 (1971)

Familial leukemia. Report of two cases in siblings
, Indian Journal of Pediatrics 37(267): 158-159 (1970)

Familial leukemia: Ph1 positive acute lymphoid leukemia of a mother and her infant
, Blut 43(4): 265-272 (1981)

Familial leukemia: description of two kindreds and a review of the genetic aspects of the disease
, Acta Haematologica 92(4): 208-211 (1994)

Familial leukemia: uncommon type of chronic lymphocytic leukemia in two sisters
, Haematologica 67(3): 406-410 (1982)

Familial levodopa-responsive parkinsonian-pyramidal syndrome
, Movement Disorders: Official Journal of the Movement Disorder Society 9(6): 673-675 (1994)

Familial lichen amyloidosis
, International Journal of Dermatology 23(3): 190-193 (1984 )

Familial lichen nitidus. The simultaneous occurrence of lichen nitidus in brothers
, Transactions of the St. John's Hospital Dermatological Society 56(2): 165-167 (1970)

Familial lichen planus. A report of nine cases from four families with a brief review of the literature
, Archives of Dermatology 119(4): 292-294 (1983)

Familial lichen ruber planus. Considerations on the infectious etiology
, Giornale Italiano di Dermatolotia. Minerva Dermatologica 45(1): 11-16 (1970)

Familial life-long persistent fever of unknown origin responding to dexamethasone and uronic acids
, American Journal of Medicine 46(1): 142-153 (1969)

Familial limb-girdle myasthenia
, Brain: a Journal of Neurology 89(1): 121-132 (1966)

Familial lipoatrophic diabetes with dominant transmission. A new syndrome
, Quarterly Journal of Medicine 43(169): 33-48 (1974)

Familial lipoprotein deficiencies
, Nihon Rinsho. Japanese Journal of Clinical Medicine 41(8): 1824-1831 (1983)

Familial lipoprotein disorders and premature coronary artery disease
, Atherosclerosis 108(Suppl): S41-S54 (1994)

Familial lipoprotein lipase and apolipoprotein C-II deficiency. Lipoprotein and apoprotein analysis, adipose tissue and hepatic lipoprotein lipase levels in seven patients and their first degree relatives
, Atherosclerosis 49(1): 55-68 (1983)

Familial lissencephaly with extreme neopallial hypoplasia
, Brain and Development 4(2): 145-151 (1982)

Familial longevity and prognosis in Hodgkin's disease
, Cancer 54(6): 1088-1092 (1984)

Familial low frequency hearing loss
, Laryngoscope 81(5): 759-771 (1971)

Familial lower esophageal rings
, New England Journal of Medicine 307(7): 443 (1982)

Familial lung disease and alpha1 antitrypsin deficiency
, Clinical Notes on Respiratory Diseases 9(4): 3-10 (1971)

Familial lupus erythematosus. 12 cases in 6 families
, La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 41(18): 1104-1110 (1965)

Familial lymphedema praecox: Meige's disease
, Plastic and Reconstructive Surgery 67(3): 362-364 (1981)

Familial lympho-histiocytosis: apropos of a 3rd case in the same family
, Marseille Medical 106(12): 1045-1053 (1969)

Familial lymphocytic thyroiditis: analysis of linkage with histocompatibility and blood groups
, Journal of Clinical Endocrinology and Metabolism 37(5): 692-697 (1973)

Familial lymphohistiocytosis
, Archives Francaises de Pediatrie 27(1): 51-61 (1970)

Familial lymphohistiocytosis apropos of 2 new cases diagnosed during life
, Pediatrie 36(4): 291-295 (1981)

Familial lymphohistiocytosis associated with lymphocytic meningitis
, Archives Francaises de Pediatrie 28(7): 757-762 (1971)

Familial lymphohistiocytosis of the nervous system
, Archives of Neurology 24(3): 270-283 (1971)

Familial lymphohistiocytosis. Anatomopathological study of 2 cases detected neonatally
, Archives Francaises de Pediatrie 39(8): 613-614 (1982)

Familial lymphohistiocytosis: a report of three cases with general review. Possible links with secondary syndromes
, Nouvelle Revue Francaise d'Hematologie 13(3): 319-337 (1973)

Familial lymphohistocytosis
, Archives Francaises de Pediatrie 22(4): 385-408 (1965)

Familial lymphoid interstitial pneumonia: a long-term follow-up
, Pediatrics 65(3): 523-528 (1980)

Familial lymphopenia with T lymphocyte defect
, Journal of Pediatrics 84(2): 178-182 (1974)

Familial macrocytosis
, Lancet 2(7686): 1319-1320 (1970)

Familial male hermaphroditism
, Birth Defects Original Article Series 10(4): 243-247 (1974)

Familial male hypogonadism in spinal and bulbar muscular atrophy of late onset (Kennedy's disease). A new cause of hypogonadism
, Archivos Espanoles de Urologia 37(1): 49-55 (1984)

Familial male precocious puberty
, Current Therapy in Endocrinology and Metabolism 5: 296-299 (1994)

Familial male pseudo-hermaphrodism of karyotype XY and ambiguous morphology
, Gynecologie et Obstetrique 67(1): 15-28 (1968)

Familial male pseudohermaphrodism caused by testicular 17-ketosteroid-reductase deficiency
, Annales d'Endocrinologie 34(5): 461-475 (1973)

Familial male pseudohermaphroditism
, Human Heredity 22(3): 225-238 (1972)

Familial male pseudohermaphroditism due to 17-20-desmolase deficiency. I. In vivo endocrine studies
, Journal of Clinical Endocrinology and Metabolism 50(5): 826-833 (1980)

Familial male pseudohermaphroditism due to a testicular 17 ketosteroid reductase defect
, Annales D'endocrinologie 34(4): 440-442 (1973)

Familial male pseudohermaphroditism due to deficiency of 5 alpha-reductase
, Clinical Endocrinology 12(4): 397-406 (1980)

Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo
, Journal of Clinical Endocrinology and Metabolism 32(5): 604-610 (1971)

Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity
, New England Journal of Medicine 291(18): 938-944 (1974)

Familial malignant carotid body chemodectoma with lymph node metastases. Light and electron microscopy study
, Annales de Pathologie 2(2): 163-167 (1982)

Familial malignant lymphoma
, New York State Journal of Medicine 80(7 Pt 1): 1111-1115 (1980)

Familial malignant melanoma and atypical disseminated moles (BK-mole syndrome)
, Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 31(1): 42-46 (1980)

Familial malignant melanomas
, Nederlands Tijdschrift Voor Geneeskunde 125(30): 1194-1198 (1981)

Familial mandibuloacral dysplasia
, British Journal of Dermatology 105(6): 719-723 (1981)

Familial manic depression, phenylketonuria and acromegaly
, Canadian Journal of Psychiatry. Revue Canadienne de Psychiatrie 27(3): 258-260 (1982)

Familial manic-depressive illness and familial Parkinson's disease: a case report
, Johns Hopkins Medical Journal 151(2): 65-70 (1982)

Familial manifestations of grouped pigmentation in macular region
, Ophthalmologica. Journal International d'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift für Augenheilkunde 152(5): 364-368 (1966)

Familial mastocytosis. Presentation of 2 cases. General review. Nosologic importance
, Annales de Dermatologie et de Syphiligraphie 98(3): 241-260 (1971)

Familial meconium ileus not associated with cystic fibrosis
, Journal of Pediatric Surgery 9(6): 821-824 (1974)

Familial mediastinal fibrosis associated with seronegative spondylarthropathy
, Arthritis and Rheumatism 26(2): 221-225 (1983)

Familial mediterranean fever
, Proceedings of the Royal Society of Medicine 65(11): 977-979 (1972)

Familial mediterranean fever in Pondicherry (India)
, Tropical and Geographical Medicine 34(2): 189-191 (1982)

Familial mediterranean fever in South India
, Journal of the Association of Physicians of India 32(4): 380-381 (1984)

Familial mediterranean fever in Yugoslavia. Case history of 2 patients with autopsy findings in one and a review of 5 patients earlier reported
, Srpski Arhiv Za Celokupno Lekarstvo 98(5): 691-709 (1970)

Familial mediterranean fever in a brother and sister treated with colchicine
, Srpski Arhiv Za Celokupno Lekarstvo 109(10): 1383-1391 (1981)

Familial mediterranean fever, amyloidosis and pregnancy
, Australian and New Zealand Journal of Obstetrics and Gynaecology 13(1): 51-53 (1973)

Familial medullary cancer of the thyroid and familial pheochromocytoma
, Actualites Endocrinologiques 13(0): 107-116 (1973)

Familial medullary carcinoma and parathyroid adenoma without pheochromocytoma. Report of two cases
, Annals of Internal Medicine 78(6): 898-901 (1973)

Familial medullary carcinoma of the thyroid
, Gp 36(3): 105-107 (1969)

Familial medullary carcinoma of the thyroid, adrenal pheochromocytoma and parathyroid hyperplasia. A syndrome of multiple endocrine neoplasia
, Radiology 107(2): 249-256 (1973)

Familial medullary carcinoma of the thyroid: clinical studies in northern New England
, Henry Ford Hospital Medical Journal 32(4): 244-245 (1984)

Familial medullary thyroid carcinoma and pheochromocytoma: epidemiologic investigations
, Journal of the National Cancer Institute 52(1): 285-287 (1974)

Familial medullary thyroid carcinoma in multiple endocrine neoplasia (MEN) IIa: diagnosis and problems in treatment
, European Journal of Cancer and Clinical Oncology 18(7): 645-650 (1982)

Familial medullary thyroid carcinoma, pheochromocytoma, and parathyroid adenoma (Sipple's syndrome). Study of a kindred
, Cancer 28(5): 1245-1254 (1971)

Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings
, Acta Neuropathologica 59(1): 70-74 (1983)

Familial megalencephaly
, Birth Defects Original Article Series 7(1): 228-230 (1971)

Familial megalencephaly or hydrocephalus?
, Neurology 24(3): 232-236 (1974)

Familial melanoma associated with dominant ultraviolet radiation sensitivity
, Cancer Research 42(7): 2909-2912 (1982)

Familial melanomas
, JAMA 220(2): 277 (1972)

Familial melanopathy with gigantic melanocytes
, American Journal of Dermatopathology 6(Suppl): 31-34 (1984)

Familial mental retardation and progressive spasticity
, Clinical Genetics 47(2): 107 (1995)

Familial mental retardation and the fragile X syndrome
, Tijdschrift Voor Kindergeneeskunde 52(1): 9-15 (1984)

Familial mental retardation with an incidental balanced t(12;16) translocation
, Southern Medical Journal 74(8): 1021-1022 (1981)

Familial mesenteric hypertension
, Revue Medico-Chirurgicale des Maladies du Foie 42(6): 237-246 (1967)

Familial metachromatic leucodystrophy--arylsulfatase A activity of leukocytes and probable carrier state
, Nihon Shonika Gakkai Zasshi. Acta Paediatrica Japonica 74(6): 590-595 (1970)

Familial metaphyseal dysplasia or Pyle's disease. Description of 2 cases
, La Chirurgia Degli Organi di Movimento 68(1): 113-119 (1982)

Familial metaphyseal dysplasia. Review of the clinical and radiologic feature of Pyle's disease
, Clinical Pediatrics 6(3): 143-149 (1967)

Familial methemoglobinemia due to diaphorase deficiency: a 3d Swiss line
, Schweizerische Medizinische Wochenschrift 96(11): 355-357 (1966)

Familial microcephalies due to cerebral malformation. Anatomical and clinical study
, Acta Neuropathologica 20(2): 96-109 (1972)

Familial microcephaly: three cases in the same sibship
, Journal de Medecine de Bordeaux et du Sud-Ouest 144(10): 1553-1555 (1967)

Familial microspherocytosis. Treatment of jaundice with phenobarbital
, Revista Clinica Espanola 124(4): 399-404 (1972)

Familial microtia with meatal atresia in father and son
, Turkish Journal of Pediatrics 16(3): 140-143 (1974)

Familial microtia with meatal atresia in two sibships
, Journal of Medical Genetics 5(4): 289-291 (1968)

Familial midgut anomalies--a spectrum of defects due to the same cause?
, American Journal of Medical Genetics 8(4): 443-446 (1981)

Familial midgut volvulus
, Surgery 72(3): 420-426 (1972)

Familial migration. Pathology of the migrant woman and newborn infant, study of risk factors and research on preventive measures
, La Revue du Praticien 34(57): 3231-3239 (1984)

Familial minor neurodevelopmental disorders
, Clinical Genetics 25(2): 148-154 (1984)

Familial misrotation-a very rare form of kidney abnormalities
, Zeitschrift für Urologie und Nephrologie 65(10): 749-755 (1972)

Familial mitochondrial myopathy with cataract
, Journal of the Neurological Sciences 45(2-3): 191-203 (1980)

Familial mitochondrial myopathy with eczema and mental retardation
, Pediatrie 35(5): 419-424 (1980)

Familial mongolism caused by transmission of a D-G 21 translocation among members of 3 generations
, Folia Hereditaria et Pathologica 16(4): 165-176 (1967)

Familial mongolism with G-G translocation in the karyotype
, Polski Tygodnik Lekarski 24(40): 1539-1541 (1969)

Familial moniliasis, defective delayed hypersensitivity, and ACTH deficiency
, Journal of Pediatrics 81(1): 198 (1972)

Familial monosaccharide malabsorption
, Bibliotheca Paediatrica 87: 101-112 (1968)

Familial morbidity in hemorrhagic fever with renal syndrome
, Pediatriia 1980(2): 61 (1980)

Familial mosaicism with G ring
, Humangenetik 7(4): 275-286 (1969)

Familial motor neuron disease with cases of amyotrophic lateral sclerosis and spinal muscular atrophy
, Rinsho Shinkeigaku 25(10): 1119-1125 (1985)

Familial motor neuron disease, non-Chamorro type: report of kinship
, Acta Neurologica Scandinavica 47(3): 341-349 (1971)

Familial motor neurone disease associated with non-specific organic dementia. A clinico-pathological study of a family
, Medical Journal of Australia 141(7): 430-433 (1984)

Familial mucosal neuromatosis: a minor form of the MEN-2b syndrome
, Journal Francais d'Ophtalmologie 7(6-7): 479-484 (1984)

Familial multicentric angiofollicular lymphoid hyperplasia
, Southern Medical Journal 76(9): 1183-1184 (1983)

Familial multicentric fibromatosis--desmoids. A report of three cases in a Jordanian family
, Cancer 24(4): 786-795 (1969)

Familial multicentric non-chromaffin paragangliomas: a case report on a patient with glomus jugulare and bilateral carotid body tumours
, Clinical Oncology 6(3): 273-275 (1980)

Familial multicentric osteolysis with recessive transmission. Four cases in a family
, Annales de Pediatrie 29(6): 441-445 (1982)

Familial multicore disease with focal loss of cross-striations and ophthalmoplegia
, Journal of the Neurological Sciences 52(1): 1-10 (1981)

Familial multifocal fibrosclerosis. Findings suggesting that retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and pseudotumor of the orbit may be different manifestations of a single disease
, Annals of Internal Medicine 66(5): 884-892 (1967)

Familial multinuclear erythroblasts with macrocytic anemia caused by ineffective erythropoiesis and increased hemolysis
, Die Medizinische Welt 42: 2280-2283 (1968)

Familial multiple (asymmetrical) lipomatosis associated with small intestinal leiomyoma
, Journal of the Association of Physicians of India 42(2): 178 (1994)

Familial multiple endocrine adenomatosis type I (MEAS I)
, Revista Medica de Chile 108(3): 221-232 (1980)

Familial multiple endocrine adenomatosis. Multiple endocrine neoplasia, type I
, Archives of Internal Medicine 129(4): 567-569 (1972)

Familial multiple endocrine adenopathy (primary hyperparathyroidism and Zollinger-Ellison syndrome) in two siblings
, Proceedings of the Royal Society of Medicine 61(7): 658-660 (1968)

Familial multiple endocrine neoplasia, type 2
, La Vie Medicale au Canada Francais 1(6): 581-582 (1972)

Familial multiple glomangiomatosis. Phlebographic record
, Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 79(1): 94-97 (1972)

Familial multiple glomus tumors and pheochromocytomas
, Annals of Otology Rhinology and Laryngology 90(1 Pt 1): 60-63 (1981)

Familial multiple melanocytic naevi--the B-K mole syndrome
, Clinical and Experimental Dermatology 6(5): 549-553 (1981)

Familial multiple myeloma. A review of thirty-seven families
, Postgraduate Medical Journal 58(675): 12-16 (1982)

Familial multiple myeloma. II. Final pathological findings in two brothers and a sister
, Journal of the National Medical Association 59(4): 278-281 (1967)

Familial multiple myeloma. Report of a case in a father and daughter. Review of the literature
, Revue du Rhumatisme 62(6): 439-445 (1995)

Familial multiple myeloma: beta myeloma in 2 sisters
, Haematologica 58(9): 565-566 (1972)

Familial multiple myeloma: the tenth reported occurrence
, American Journal of the Medical Sciences 254(6): 848-850 (1967)

Familial multiple naevogene melanomas. Electronmicroscopical findings in pigmented moles of the B-K-mole syndrome
, Zeitschrift für Hautkrankheiten 56(14): 931-941 (1981)

Familial multiple peripheral nerve entrapments--an unusual manifestation of a peripheral neuropathy
, Transactions of the American Neurological Association 98: 267-269 (1973)

Familial multiple polyposis with adenocarcinoma in situ of the colon: report of a case
, Journal of the American Osteopathic Association 68(4): 366-371 (1968)

Familial multiple polyposis. Surgery core 1972
, Journal of the South Carolina Medical Association 69(10): 367-369 (1973)

Familial multiple polyposis: a "curable" disease
, Wisconsin Medical Journal 70(11): 230-231 (1971)

Familial multiple polyposis: research tool for investigating the etiology of carcinoma of the colon?
, Diseases of the Colon and Rectum 11(1): 17-31 (1968)