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M Zeviani

Showing results (51-60 of 184) with videos related to

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Mitochondrion|August 27, 2005
Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patientsF Carrara, P F Chinnery, P Yu-Wai-Man, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Acta Neurologica Scandinavica|March 1, 1993
Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 casesS Franceschetti, C Antozzi, S Binelli, et al.
Current Molecular Medicine|October 18, 2014
Mitochondrial Diseases in ChildhoodA Ardissone, E Lamantea, F Invernizzi, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Annals of Neurology|February 24, 2001
A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patientsP Corona, C Antozzi, F Carrara, et al.
Human Molecular Genetics|February 22, 2001
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndromeV Petruzzella, R Vergari, I Puzziferri, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathyV Scaioli, C Antozzi, F Villani, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Science (New York, N.Y.)|April 21, 1989
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNAE A Schon, R Rizzuto, C T Moraes, et al.
Pageof 19

Showing results (51-60 of 184) with videos related to

Sort By:
Pageof 19
Mitochondrion|August 27, 2005
Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patientsF Carrara, P F Chinnery, P Yu-Wai-Man, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Acta Neurologica Scandinavica|March 1, 1993
Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 casesS Franceschetti, C Antozzi, S Binelli, et al.
Current Molecular Medicine|October 18, 2014
Mitochondrial Diseases in ChildhoodA Ardissone, E Lamantea, F Invernizzi, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Annals of Neurology|February 24, 2001
A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patientsP Corona, C Antozzi, F Carrara, et al.
Human Molecular Genetics|February 22, 2001
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndromeV Petruzzella, R Vergari, I Puzziferri, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathyV Scaioli, C Antozzi, F Villani, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Science (New York, N.Y.)|April 21, 1989
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNAE A Schon, R Rizzuto, C T Moraes, et al.
Pageof 19