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A Lombes

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Journal of Inherited Metabolic Disease|January 1, 1996
Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.
Enzyme|January 1, 1987
Hyperketotic states due to inherited defects of ketolysisJ M Saudubray, N Specola, B Middleton, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology]A Lombes, F Hervé, H Ogier, et al.
Annals of Neurology|June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNAW D Graf, S M Sumi, M K Copass, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1990
Mitochondrial myopathy and myoclonic epilepsyW O Arruda, L F Torres, A Lombes, 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.
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.
Anales Espanoles De Pediatria|February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]M Roig Quilis, J Sánchez Esteban, A Lombes, 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.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.
Enzyme|January 1, 1987
Hyperketotic states due to inherited defects of ketolysisJ M Saudubray, N Specola, B Middleton, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology]A Lombes, F Hervé, H Ogier, et al.
Annals of Neurology|June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNAW D Graf, S M Sumi, M K Copass, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1990
Mitochondrial myopathy and myoclonic epilepsyW O Arruda, L F Torres, A Lombes, 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.
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.
Anales Espanoles De Pediatria|February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]M Roig Quilis, J Sánchez Esteban, A Lombes, 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.
Pageof 4