Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Rustin

Showing results (61-70 of 157) with videos related to

Pageof 16
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscleD Chretien, M Pourrier, T Bourgeron, et al.
The Journal of Pediatrics|November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndromeT Ferlin, P Landrieu, C Rambaud, et al.
Neuropediatrics|December 19, 2003
Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiencyN Darin, A-R Moslemi, S Lebon, et al.
Free Radical Research|November 8, 2001
Human cultured skin fibroblasts survive profound inherited ubiquinone depletionV Geromel, N Kadhom, I Ceballos-Picot, et al.
Heart (British Cardiac Society)|March 22, 2002
Idebenone and reduced cardiac hypertrophy in Friedreich's ataxiaA O Hausse, Y Aggoun, D Bonnet, et al.
The Journal of Clinical Investigation|March 1, 1993
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)A Rötig, V Cormier, P Chatelain, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Biochemical and molecular investigations in respiratory chain deficienciesP Rustin, D Chretien, T Bourgeron, et al.
Journal of Hepatology|March 9, 2000
Fatal lactic acidosis and liver steatosis associated with didanosine and stavudine treatment: a respiratory chain dysfunction?F G Brivet, I Nion, B Mégarbane, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 22, 1999
[Metabolic and genetic investigations in childhood cardiomyopathies]D Bonnet, P Rustin, A Rötig, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome)A Rötig, V Cormier, P Chatelain, et al.
Pageof 16

Showing results (61-70 of 157) with videos related to

Sort By:
Pageof 16
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscleD Chretien, M Pourrier, T Bourgeron, et al.
The Journal of Pediatrics|November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndromeT Ferlin, P Landrieu, C Rambaud, et al.
Neuropediatrics|December 19, 2003
Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiencyN Darin, A-R Moslemi, S Lebon, et al.
Free Radical Research|November 8, 2001
Human cultured skin fibroblasts survive profound inherited ubiquinone depletionV Geromel, N Kadhom, I Ceballos-Picot, et al.
Heart (British Cardiac Society)|March 22, 2002
Idebenone and reduced cardiac hypertrophy in Friedreich's ataxiaA O Hausse, Y Aggoun, D Bonnet, et al.
The Journal of Clinical Investigation|March 1, 1993
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)A Rötig, V Cormier, P Chatelain, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Biochemical and molecular investigations in respiratory chain deficienciesP Rustin, D Chretien, T Bourgeron, et al.
Journal of Hepatology|March 9, 2000
Fatal lactic acidosis and liver steatosis associated with didanosine and stavudine treatment: a respiratory chain dysfunction?F G Brivet, I Nion, B Mégarbane, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 22, 1999
[Metabolic and genetic investigations in childhood cardiomyopathies]D Bonnet, P Rustin, A Rötig, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome)A Rötig, V Cormier, P Chatelain, et al.
Pageof 16