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Showing articles 0 to 6 of 6 Filter Applied: muscular dystrophy,congenital (Click to remove) A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes Neurol 102:e209258, Lail,G.,et al, 2024 The Muscular Dystrophies BMJ 317:991-995, Emery,A.E.H., 1998 Diagnosis and Etiology of Congenital Muscular Dystrophy Neurol 71:312-321,308, Peat,R.A.,et al., 2008 Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Night-Time Nasal Ventilation in Neuromuscular Disease Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990 Showing articles 0 to 6 of 6