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M Zeviani

Showing results (131-140 of 184) with videos related to

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Human Mutation|April 24, 2001
Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiencyM O Péquignot, R Dey, M Zeviani, et al.
Archives of Neurology|November 1, 1986
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiencyM Zeviani, D H Van Dyke, S Servidei, et al.
Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Neurology|April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutationsS Winterthun, G Ferrari, L He, et al.
The New England Journal of Medicine|May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndromeC T Moraes, S DiMauro, M Zeviani, et al.
Cell Death and Differentiation|July 25, 2015
Reduced mitochondrial Ca(2+) transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenaseV Granatiero, V Giorgio, T Calì, et al.
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
Gene|January 1, 1987
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidaseM Zeviani, M Nakagawa, J Herbert, et al.
Pageof 19

Showing results (131-140 of 184) with videos related to

Sort By:
Pageof 19
Human Mutation|April 24, 2001
Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiencyM O Péquignot, R Dey, M Zeviani, et al.
Archives of Neurology|November 1, 1986
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiencyM Zeviani, D H Van Dyke, S Servidei, et al.
Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Neurology|April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutationsS Winterthun, G Ferrari, L He, et al.
The New England Journal of Medicine|May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndromeC T Moraes, S DiMauro, M Zeviani, et al.
Cell Death and Differentiation|July 25, 2015
Reduced mitochondrial Ca(2+) transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenaseV Granatiero, V Giorgio, T Calì, et al.
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
Gene|January 1, 1987
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidaseM Zeviani, M Nakagawa, J Herbert, et al.
Pageof 19