Title: | Congenital muscular dystrophies |
Journal : | Handbook of Clinical Neurology (Pediatric Neurology), 113, 3rd series, chap. 143 |
Authors: | Kirschner J |
Material Type: | Article |
Publication Date: | 2013 |
Size: | p. 1377-1385 |
Languages: | English |
Keywords : | congenital muscular dystrophy ; congenital muscular dystrophy with primary merosin deficiency ; creatine kinase ; differential diagnosis ; epidemiology ; Fukuyama congenital muscular dystrophy ; hypertrophic progressive congenital muscular dystrophy ; MRI ; muscle histopathology ; muscle-eye-brain disease related to POMGNT1 ; rigid spine syndrome ; syndrome de Walker-Warburg avec déficit de la glycosylation de l'alpha-dystroglycane ; Ullrich congenital muscular dystrophy |
Abstract: |
Accès au résumé Pubmed/to pubmed abstract |
Pubmed / DOI : | DOI : 10.1016/B978-0-444-59565-2.00008-3 |
See also : |