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Showing articles 0 to 8 of 8 Filter Applied: cultured skin fibroblasts (Click to remove) 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 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 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 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 8 of 8