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A Rotig

Showing results (1-10 of 11) with videos related to

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Pediatrie|January 1, 1991
[Metabolic, enzymological and molecular assessment of mitochondrial cytopathies]A Munnich, A Rotig
Mechanisms of Ageing and Development|May 10, 2000
For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?P Rustin, J C von Kleist-Retzow, Z Vajo, et al.
American Journal of Human Genetics|April 1, 1991
Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathyV Cormier, A Rotig, M Tardieu, et al.
The Biochemical Journal|January 15, 1995
Perinatal maturation of rat kidney mitochondriaB Prieur, L Cordeau-Lossouarn, A Rotig, et al.
Nephron|January 1, 1997
Renal failure from mitochondrial cytopathiesM Buemi, A Allegra, A Rotig, et al.
European Journal of Medical Genetics|October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.
Human Genetics|January 1, 1990
Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiencyA Pelet, A Rotig, C Bonaïti-Pellié, 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.
The Journal of Pediatrics|December 1, 1992
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatrie|January 1, 1991
[Metabolic, enzymological and molecular assessment of mitochondrial cytopathies]A Munnich, A Rotig
Mechanisms of Ageing and Development|May 10, 2000
For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?P Rustin, J C von Kleist-Retzow, Z Vajo, et al.
American Journal of Human Genetics|April 1, 1991
Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathyV Cormier, A Rotig, M Tardieu, et al.
The Biochemical Journal|January 15, 1995
Perinatal maturation of rat kidney mitochondriaB Prieur, L Cordeau-Lossouarn, A Rotig, et al.
Nephron|January 1, 1997
Renal failure from mitochondrial cytopathiesM Buemi, A Allegra, A Rotig, et al.
European Journal of Medical Genetics|October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.
Human Genetics|January 1, 1990
Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiencyA Pelet, A Rotig, C Bonaïti-Pellié, 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.
The Journal of Pediatrics|December 1, 1992
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
Pageof 2