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Showing articles 0 to 8 of 8 Filter Applied: genetic neurologic disorders (Click to remove) Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy NEJM 388:2379-2387, Case 19-2023, 2023 Duchenne Muscular Dystrophy BMJ 368:L7012, Fox, H.,et al, 2020 The Limbic-Girdle Muscular Dystrophies Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014 Diagnosis and New Treatments in Muscular Dystrophies JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009 Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy NEJM 334:362-366, Fadic,R.,et al, 1996 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982 The Spectrum of Mild X-Linked Recessive Muscular Dystrophy Arch Neurol 34:408, Ringer,S.P.,et al, 1977 Showing articles 0 to 8 of 8