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Showing articles 0 to 10 of 10 Filter Applied: cultured skin fibroblasts (Click to remove) Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 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 Late Onset Globoid Cell Leukodystrophy JNNP 54:1011-1012, Grewal,R.P.,et al, 1991 Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV Stroke 21:626-632, Schievink,W.I.,et al, 1990 Acute Profound Dystonia in Infants with Glutaric Acidemia Pediatrics 83:228-234, Bergman,I.,et al, 1989 Showing articles 0 to 10 of 10