+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

A new congenital myopathy



A new congenital myopathy



Acta Paediatrica 91(6): 727-728




Please choose payment method:






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

Accession: 045079694

Download citation: RISBibTeXText

PMID: 12162615

DOI: 10.1111/j.1651-2227.2002.tb03315.x


Related references

Surgery for foot deformity in patients with congenital myopathy (multicore disease, congenital fiber-type disproportion, and centronuclear myopathy). Journal of Pediatric Orthopedics. Part B 18(4): 179-184, 2009

Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation. Acta Neuropathologica 124(4): 575-581, 2012

Congenital Nonprogressive Myopathy. Central Core Disease and Nemaline Myopathy in one Family. Neurology 15: 371-381, 1965

Congenital autophagic vacuolar myopathy is allelic to X-linked myopathy with excessive autophagy. Neurology 84(16): 1714-1716, 2015

Nonspecific congenital myopathy (minimal change myopathy): a case report. Brain and Development 9(1): 61-64, 1987

Monomelic myopathy. Congenital hypertrophic myotonic myopathy limited to one extremity. Archives of Neurology 17(1): 69-77, 1967

Zebra body myopathy: a second case of ultrastructurally distinct congenital myopathy. Journal of Child Neurology 2(4): 307-310, 1987

Severe congenital actin related myopathy with myofibrillar myopathy features. Neuromuscular Disorders 25(6): 488-492, 2015

Congenital myopathy with mosaic fibers and interlacing sarcomeres: A new structural myopathy. Acta Neuropathologica 96(6): 643-650, 1998

Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years. Journal of Neuromuscular Diseases 2(2): 167-174, 2015

Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathy. Neuropediatrics 32(4): 196-205, 2001

Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy). Brain and Development 12(4): 427-430, 1990

Myopathy with hexagonally cross-linked tubular arrays: A new autosomal dominant or sporadic congenital myopathy. Annals of Neurology 45(4): 512-515, 1999