Enter your terms above and click the 'Search' button.

Showing articles 0 to 13 of 13 Filter Applied: gene (Click to remove) Muscular Dystrophies Lancet 394:2025-2038, Mercuri, E.,et al, 2019 Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies Neurol 75:316-323,298, Paradas,C., et al, 2010 New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy JNNP 81:946-953, Klinge,L.,et al, 2010 Diagnosis and New Treatments in Muscular Dystrophies JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009 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 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995 Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy Lancet 346:741-742, Brahe,C.,et al, 1995 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 DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis Hum Genet 82:55-58, Defesche,J.C.,et al, 1989 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Showing articles 0 to 13 of 13