EurekaMag.com logo
+ Site Statistics
References:
52,654,530
Abstracts:
29,560,856
PMIDs:
28,072,755
+ Search Articles
+ Subscribe to Site Feeds
EurekaMag Most Shared ContentMost Shared
EurekaMag PDF Full Text ContentPDF Full Text
+ PDF Full Text
Request PDF Full TextRequest PDF Full Text
+ Follow Us
Follow on FacebookFollow on Facebook
Follow on TwitterFollow on Twitter
Follow on LinkedInFollow on LinkedIn

+ Translate

Recurrent arterial thrombotic disease on young onset and protein S deficiency



Recurrent arterial thrombotic disease on young onset and protein S deficiency



Blood Coagulation and Fibrinolysis 9(7): 667-668




(PDF emailed within 0-6 h: $19.90)

Accession: 033119295

Download citation: RISBibTeXText

PMID: 9863720

DOI: 10.1097/00001721-199810000-00018



Related references

Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease. Thrombosis and Haemostasis 73(5): 743-745, 1995

Child-onset and adolescent-onset acquired thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency: a cohort study of the French national registry for thrombotic microangiopathy. Lancet. Haematology 3(11): E537-E546, 2016

Adult-onset renal thrombotic microangiopathy and pulmonary arterial hypertension in cobalamin C deficiency. Lancet 386(9997): 1011-1012, 2015

Hereditary protein S deficiency in young adults with arterial occlusive disease. Thrombosis and Haemostasis 64(2): 206-210, 1990

Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy. Lancet. Haematology 3(5): E237-E245, 2018

Inherited heterozygous protein C deficiency and dysfunctional protein S with recurrent venous thrombotic diseases: a study of three generations of a Japanese family. Internal Medicine 31(10): 1197-1200, 1992

Protein-S deficiency in young patients with thrombotic brain infarction. Schweizerische Medizinische Wochenschrift 119(16): 489-492, 1989

Acquired protein S deficiency with primary antiphospholipid syndrome and recurrent thrombotic events: report of a case. Revue du Rhumatisme 62(11): 810-811, 1995

A positive family history for premature cardiovascular disease identifies patients prone to recurrent arterial thrombotic events. European Journal of Preventive Cardiology 19(6): 1465-1473, 2013

Factor V Leiden and increased risk for arterial thrombotic disease in young Brazilian patients. Blood Coagulation and Fibrinolysis 17(4): 271-275, 2006

A new hereditary thrombotic disease--protein C deficiency. Duodecim; Laaketieteellinen Aikakauskirja 100(17): 1089-1095, 1984

Deficiency of protein C in congenital thrombotic disease. Journal of Clinical Investigation 68(5): 1370-1373, 1981

Severe protein C deficiency in congenital thrombotic disease--description of an immunoenzymological assay for protein C determination. Thrombosis and Haemostasis 53(3): 293-296, 1985

Prevalence of protein c and protein s deficiency in patients with thrombotic disease. Thrombosis Research (SUPPL 6): 135, 1986

Familial thrombotic disease due to plasma protein s deficiency. Haemostasis: 84, 1985