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Current Opinion in Neurology|December 1, 1996
Fatty acid mitochondrial beta-oxidation and hypoglycaemia in childrenF Taroni, G UzielLife Sciences|July 17, 2003
Effects of the testosterone metabolite dihydrotestosterone and 5 alpha-androstan-3 alpha,17 beta-diol on very long chain fatty acid metabolism in X-adrenoleukodystrophic fibroblastsA Petroni, M Blasevich, G UzielJournal of Inherited Metabolic Disease|January 1, 1996
Neurological presentations of mitochondrial diseasesM Zeviani, B Bertagnolio, G UzielMuscle & Nerve|July 1, 1988
Carnitine stimulation of pyruvate dehydrogenase complex (PDHC) in isolated human skeletal muscle mitochondriaG Uziel, B Garavaglia, S Di DonatoClinica Chimica Acta; International Journal of Clinical Chemistry|May 16, 1984
Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiencyS Di Donato, M Rimoldi, B Garavaglia, et al.Neuroscience Letters|September 1, 2004
New findings on X-linked Adrenoleukodystrophy: 5alpha-reductase isoform 2 relative gene expression is modified in affected fibroblastsA Petroni, M Cappa, M Blasevich, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduriaI Moroni, L D'Incerti, L Farina, et al.Neuroradiology|December 22, 1998
L-2-Hydroxyglutaric aciduria: MRI in seven casesL D'Incerti, L Farina, I Moroni, et al.Developmental Neuroscience|January 1, 1991
Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathyG Uziel, E Bertini, P Bardelli, et al.Pageof 8