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 (91-100 of 157) with videos related to

Pageof 16
Sort By:
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
The investigation of respiratory chain disorders in heart using endomyocardial biopsiesP Rustin, J Lebidois, D Chretien, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2001
Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON miceL Sörensen, M Ekstrand, J P Silva, et al.
Nature Genetics|October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyT Bourgeron, P Rustin, D Chretien, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical presentation of mitochondrial disorders in childhoodA Munnich, A Rötig, D Chretien, et al.
Journal of the Neurological Sciences|April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiencyE Boitier, F Degoul, I Desguerre, et al.
Nature Genetics|March 21, 1998
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in miceN G Larsson, J Wang, H Wilhelmsson, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenoneT Lerman-Sagie, P Rustin, D Lev, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1997
Severe complex I deficiency in a case of neonatal-onset lactic acidosis and fatal liver failureM Mazzella, R Cerone, W Bonacci, et al.
Pageof 16

Showing results (91-100 of 157) with videos related to

Sort By:
Pageof 16
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
The investigation of respiratory chain disorders in heart using endomyocardial biopsiesP Rustin, J Lebidois, D Chretien, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2001
Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON miceL Sörensen, M Ekstrand, J P Silva, et al.
Nature Genetics|October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyT Bourgeron, P Rustin, D Chretien, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical presentation of mitochondrial disorders in childhoodA Munnich, A Rötig, D Chretien, et al.
Journal of the Neurological Sciences|April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiencyE Boitier, F Degoul, I Desguerre, et al.
Nature Genetics|March 21, 1998
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in miceN G Larsson, J Wang, H Wilhelmsson, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenoneT Lerman-Sagie, P Rustin, D Lev, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1997
Severe complex I deficiency in a case of neonatal-onset lactic acidosis and fatal liver failureM Mazzella, R Cerone, W Bonacci, et al.
Pageof 16