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S Servidei

Showing results (121-130 of 146) with videos related to

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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.
The American Journal of Medicine|August 15, 2001
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradicationV Cicconi, E Carloni, F Franceschi, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, 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.
Neurology|February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approachH J Tritschler, E Bonilla, A Lombes, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
American Journal of Medical Genetics|February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entityM Sabatelli, T Mignogna, G Lippi, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
The American Journal of Pathology|December 1, 1988
Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophyE Bonilla, B Schmidt, C E Samitt, et al.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
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.
The American Journal of Medicine|August 15, 2001
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradicationV Cicconi, E Carloni, F Franceschi, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, 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.
Neurology|February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approachH J Tritschler, E Bonilla, A Lombes, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
American Journal of Medical Genetics|February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entityM Sabatelli, T Mignogna, G Lippi, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
The American Journal of Pathology|December 1, 1988
Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophyE Bonilla, B Schmidt, C E Samitt, et al.
Pageof 15