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Showing articles 0 to 13 of 13 Filter Applied: cardiomyopathy (Click to remove) Metabolic Lipid Muscle Disorders: Biomarkers and Treatment Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019 Alcohol and Alcoholism Adams & Victors Principles of Neurology Chp 42, pg 1186, Ropper, A.H.,et al, 2014 Extension of the Clinical Spectrum of Danon Disease Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy NEJM 334:362-366, Fadic,R.,et al, 1996 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency Neurol 42:128-130, Riggs,J.E.,et al, 1992 Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991 Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis Neuropediatrics 19:62-71, Voit,T.,et al, 1988 Mendelian Etiologies of Stroke Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Showing articles 0 to 13 of 13