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Journal of Inherited Metabolic Disease|June 23, 2000
Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegenerationS Di DonatoNeurology|June 1, 1983
Skeletal muscle NAD+(P) and NADP+-dependent malic enzyme in Friedreich's ataxiaE Bottacchi, S Di DonatoNeurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2002
Cerebellar/spinocerebellar syndromesC Mariotti, S Di DonatoThe International Journal of Biochemistry|January 1, 1988
Purification and properties of cytosolic malic enzyme from human skeletal muscleF Taroni, S Di DonatoAnnals of Neurology|December 1, 1984
Muscle fiber degeneration and necrosis in muscular dystrophy and other muscle diseases: cytochemical and immunocytochemical dataF Cornelio, I DonesBiochimica Et Biophysica Acta|December 18, 1987
Evidence for two distinct mitochondrial malic enzymes in human skeletal muscle: purification and properties of the NAD(P)+-dependent enzymeF Taroni, C Gellera, S Di DonatoMuscle & Nerve|July 1, 1988
Carnitine stimulation of pyruvate dehydrogenase complex (PDHC) in isolated human skeletal muscle mitochondriaG Uziel, B Garavaglia, S Di DonatoNeurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 4, 2001
The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxiasS Di Donato, C Gellera, C MariottiBollettino Della Societa Italiana Di Biologia Sperimentale|June 30, 1984
[The ratio of calcium carbonate/organic matrix in the valves of Mytilus galloprovincialis as an indication of marine pollution]M D'Agostino, S Di Donato, P MorricaNeurology|April 1, 1986
Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes, fibroblasts, and muscle mitochondriaG Finocchiaro, F Taroni, S Di DonatoPageof 16