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Showing articles 0 to 10 of 10 Filter Applied: cultured skin fibroblasts (Click to remove) Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Niemann-Pick Disease Type C: Two Cases and an Update Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000 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 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 Niemann-Pick Disease Type C from Bench to Bedside JAMA 276:561-564, Schiffmann,R., 1996 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Infantile CNS Spongy Degeneration-14 Cases:Clinical Update Neurol 40:1876-1882, Gascon,G.G.,et al, 1990 Showing articles 0 to 10 of 10