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Showing articles 0 to 9 of 9 Filter Applied: cultured skin fibroblasts (Click to remove) 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 Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 Niemann-Pick Disease Type C from Bench to Bedside JAMA 276:561-564, Schiffmann,R., 1996 Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV Stroke 21:626-632, Schievink,W.I.,et al, 1990 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Showing articles 0 to 9 of 9