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Showing articles 0 to 8 of 8 Filter Applied: cultured skin fibroblasts (Click to remove) Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 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 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 Adult-Onset Metachromatic Leukodystrophy Presenting as Isolated Peripheral Neuropathy Neurol 42:1396-1398, Fressinaud,C.,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 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Showing articles 0 to 8 of 8