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Showing articles 0 to 12 of 12 Filter Applied: molecular genetics (Click to remove) Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet Neurol 46:1133-1137, Pareyson,D.,et al, 1996 Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities Neurol 44:2250-2252, Gouider,R.,et al, 1994 Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis Neurol 44:2253-2257, Chance,P.F.,et al, 1994 Muscular Dystrophies Lancet 394:2025-2038, Mercuri, E.,et al, 2019 LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 The Muscular Dystrophies BMJ 317:991-995, Emery,A.E.H., 1998 Mutations in the Sarcoglycan Genes in Patients with Myopathy NEJM 336:618-624, Duggan,D.J.,et al, 1997 Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy Lancet 346:741-742, Brahe,C.,et al, 1995 Clinicopath Conf Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992 Showing articles 0 to 12 of 12