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P Rustin

Showing results (111-120 of 157) with videos related to

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Irish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.
Nature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
European Heart Journal|August 26, 1998
Efficiency of metabolic screening in childhood cardiomyopathiesD Bonnet, P de Lonlay, I Gautier, et al.
Antisense & Nucleic Acid Drug Development|July 12, 2001
Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomesV Geromel, A Cao, D Briane, et al.
Neuropediatrics|August 25, 2001
Respiratory chain deficiency in Alpers syndromeM Gauthier-Villars, P Landrieu, V Cormier-Daire, et al.
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
The Journal of Clinical Investigation|November 1, 1990
Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancyA Rötig, V Cormier, S Blanche, et al.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
American Journal of Human Genetics|October 3, 2000
Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathyI Valnot, S Osmond, N Gigarel, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
Irish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.
Nature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
European Heart Journal|August 26, 1998
Efficiency of metabolic screening in childhood cardiomyopathiesD Bonnet, P de Lonlay, I Gautier, et al.
Antisense & Nucleic Acid Drug Development|July 12, 2001
Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomesV Geromel, A Cao, D Briane, et al.
Neuropediatrics|August 25, 2001
Respiratory chain deficiency in Alpers syndromeM Gauthier-Villars, P Landrieu, V Cormier-Daire, et al.
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
The Journal of Clinical Investigation|November 1, 1990
Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancyA Rötig, V Cormier, S Blanche, et al.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
American Journal of Human Genetics|October 3, 2000
Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathyI Valnot, S Osmond, N Gigarel, et al.
Pageof 16