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P Rustin

Showing results (121-130 of 157) with videos related to

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The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1992
[Enzymatic activities of the mitochondrial respiratory chain in child cardiomyopathies. 34 cases prospectively studied by endomyocardial biopsy]D Sidi, J Le Bidois, J F Piéchaud, et al.
The Journal of Pediatrics|January 1, 1994
Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophyV Cormier-Daire, J P Bonnefont, P Rustin, et al.
American Journal of Medical Genetics|December 30, 1996
Craniofacial anomalies and malformations in respiratory chain deficiencyV Cormier-Daire, P Rustin, A Rötig, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, et al.
American Journal of Human Genetics|July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiencyJ C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
British Journal of Haematology|June 1, 1994
Refractory anaemia and mitochondrial cytopathy in childhoodB Bader-Meunier, A Rötig, F Mielot, et al.
Oncogene|April 5, 2011
BH3 mimetics activate multiple pro-autophagic pathwaysS A Malik, I Orhon, E Morselli, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
Pageof 16

Showing results (121-130 of 157) with videos related to

Sort By:
Pageof 16
The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1992
[Enzymatic activities of the mitochondrial respiratory chain in child cardiomyopathies. 34 cases prospectively studied by endomyocardial biopsy]D Sidi, J Le Bidois, J F Piéchaud, et al.
The Journal of Pediatrics|January 1, 1994
Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophyV Cormier-Daire, J P Bonnefont, P Rustin, et al.
American Journal of Medical Genetics|December 30, 1996
Craniofacial anomalies and malformations in respiratory chain deficiencyV Cormier-Daire, P Rustin, A Rötig, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, et al.
American Journal of Human Genetics|July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiencyJ C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
British Journal of Haematology|June 1, 1994
Refractory anaemia and mitochondrial cytopathy in childhoodB Bader-Meunier, A Rötig, F Mielot, et al.
Oncogene|April 5, 2011
BH3 mimetics activate multiple pro-autophagic pathwaysS A Malik, I Orhon, E Morselli, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
Pageof 16