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S Di Donato

Showing results (1-10 of 97) with videos related to

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Italian Journal of Neurological Sciences|August 10, 2000
The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxiasS Di Donato
Journal of Inherited Metabolic Disease|June 23, 2000
Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegenerationS Di Donato
Current Opinion in Neurology|December 1, 1996
Cellular models for pathogenesis in mitochondrial diseasesS Di Donato
The Italian Journal of Biochemistry|July 1, 1984
Primary and secondary carnitine deficiency in manS Di Donato
Progress in Clinical and Biological Research|January 1, 1990
Short-chain and medium-chain acylCoA dehydrogenases are lowered in riboflavin-responsive lipid myopathies with multiple acylCoA dehydrogenase deficiencyS Di Donato, C Gellera
Neurology|June 1, 1983
Skeletal muscle NAD+(P) and NADP+-dependent malic enzyme in Friedreich's ataxiaE Bottacchi, S Di Donato
Rivista Di Patologia Nervosa E Mentale|August 1, 1976
The syndrome of carnitine deficiencyS Di Donato, F Cornelio
Neurological 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 Donato
Journal of Neurology|January 1, 1985
Myopathies due to enzyme deficienciesF Cornelio, S Di Donato
The International Journal of Biochemistry|January 1, 1988
Purification and properties of cytosolic malic enzyme from human skeletal muscleF Taroni, S Di Donato
Pageof 10

Showing results (1-10 of 97) with videos related to

Sort By:
Pageof 10
Italian Journal of Neurological Sciences|August 10, 2000
The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxiasS Di Donato
Journal of Inherited Metabolic Disease|June 23, 2000
Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegenerationS Di Donato
Current Opinion in Neurology|December 1, 1996
Cellular models for pathogenesis in mitochondrial diseasesS Di Donato
The Italian Journal of Biochemistry|July 1, 1984
Primary and secondary carnitine deficiency in manS Di Donato
Progress in Clinical and Biological Research|January 1, 1990
Short-chain and medium-chain acylCoA dehydrogenases are lowered in riboflavin-responsive lipid myopathies with multiple acylCoA dehydrogenase deficiencyS Di Donato, C Gellera
Neurology|June 1, 1983
Skeletal muscle NAD+(P) and NADP+-dependent malic enzyme in Friedreich's ataxiaE Bottacchi, S Di Donato
Rivista Di Patologia Nervosa E Mentale|August 1, 1976
The syndrome of carnitine deficiencyS Di Donato, F Cornelio
Neurological 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 Donato
Journal of Neurology|January 1, 1985
Myopathies due to enzyme deficienciesF Cornelio, S Di Donato
The International Journal of Biochemistry|January 1, 1988
Purification and properties of cytosolic malic enzyme from human skeletal muscleF Taroni, S Di Donato
Pageof 10