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A F Miranda

Showing results (91-100 of 104) with videos related to

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Neurology|January 27, 1998
Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogenesesR Carrozzo, M Hirano, B Fromenty, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.
Neurology|January 1, 1990
Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndromeS Shanske, C T Moraes, A Lombes, et al.
Genomics|April 1, 1988
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32M Zeviani, B T Darras, R Rizzuto, et al.
Neurology|August 1, 1990
Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathyE Bonilla, D S Younger, H W Chang, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, 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.
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.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Neurology|January 27, 1998
Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogenesesR Carrozzo, M Hirano, B Fromenty, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.
Neurology|January 1, 1990
Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndromeS Shanske, C T Moraes, A Lombes, et al.
Genomics|April 1, 1988
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32M Zeviani, B T Darras, R Rizzuto, et al.
Neurology|August 1, 1990
Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathyE Bonilla, D S Younger, H W Chang, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, 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.
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.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Pageof 11