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A Lombes

Showing results (11-20 of 38) with videos related to

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Neurology|November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processingR N Van Coster, D C De Vivo, D Blake, et al.
Journal De Genetique Humaine|December 1, 1989
[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset]J M Saudubray, S Lyonnet, A Lombes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Diagnostic approach to metabolic myopathies]J M Cuisset, J C Cuvellier, C De Sèze, et al.
Journal of Medical Genetics|September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutationA Saada, A Shaag, S Arnon, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
Metabolic Brain Disease|March 26, 2009
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhoodE Lagrue, B Abert, L Nadal, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficienciesE A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial encephalomyopathiesS DiMauro, M Zeviani, C T Moraes, et al.
Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.
Journal of Medical Genetics|January 13, 2010
A novel FTL insertion causing neuroferritinopathyS Batey, I Vuillaume, D Devos, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Neurology|November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processingR N Van Coster, D C De Vivo, D Blake, et al.
Journal De Genetique Humaine|December 1, 1989
[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset]J M Saudubray, S Lyonnet, A Lombes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Diagnostic approach to metabolic myopathies]J M Cuisset, J C Cuvellier, C De Sèze, et al.
Journal of Medical Genetics|September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutationA Saada, A Shaag, S Arnon, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
Metabolic Brain Disease|March 26, 2009
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhoodE Lagrue, B Abert, L Nadal, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficienciesE A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial encephalomyopathiesS DiMauro, M Zeviani, C T Moraes, et al.
Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.
Journal of Medical Genetics|January 13, 2010
A novel FTL insertion causing neuroferritinopathyS Batey, I Vuillaume, D Devos, et al.
Pageof 4