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B Mousson

Showing results (11-20 of 48) with videos related to

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Molecular & General Genetics : MGG|November 27, 1996
Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathiesJ M Collombet, G Mandon, R Dumoulin, et al.
Molecular and Cellular Probes|October 1, 1996
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intoleranceR Dumoulin, I Sagnol, T Ferlin, et al.
La Revue De Medecine Interne|May 1, 1991
[Mitochondrial cytopathies]B Mousson, I Maire, H Carrier, et al.
Revue Neurologique|July 31, 1998
[MNGIE syndrome in 2 siblings]M Debouverie, M Wagner, X Ducrocq, et al.
Journal of Hepatology|February 2, 1999
Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosisP H Ducluzeau, A Lachaux, R Bouvier, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reactionT Ferlin, G Guironnet, M C Barnoux, et al.
Presse Medicale (Paris, France : 1983)|November 19, 1988
[Recurrent rhabdomyolysis and deficiency of carnitine palmityl transferase. Evidence of the responsibility of a mutant in 2 brothers]J L Dupond, B Mousson, F Guerber, et al.
Journal of the Neurological Sciences|March 1, 1996
Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cellsJ Villard, A Fischer, G Mandon, et al.
Annales De Biologie Clinique|January 1, 1995
Serum 5'-nucleotidase and alkaline phosphatase activities after high dose chemotherapy and bone marrow transplantation in cases of malignancy in childrenP Clerc-Renaud, G Souillet, C Lahet, 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.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Molecular & General Genetics : MGG|November 27, 1996
Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathiesJ M Collombet, G Mandon, R Dumoulin, et al.
Molecular and Cellular Probes|October 1, 1996
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intoleranceR Dumoulin, I Sagnol, T Ferlin, et al.
La Revue De Medecine Interne|May 1, 1991
[Mitochondrial cytopathies]B Mousson, I Maire, H Carrier, et al.
Revue Neurologique|July 31, 1998
[MNGIE syndrome in 2 siblings]M Debouverie, M Wagner, X Ducrocq, et al.
Journal of Hepatology|February 2, 1999
Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosisP H Ducluzeau, A Lachaux, R Bouvier, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reactionT Ferlin, G Guironnet, M C Barnoux, et al.
Presse Medicale (Paris, France : 1983)|November 19, 1988
[Recurrent rhabdomyolysis and deficiency of carnitine palmityl transferase. Evidence of the responsibility of a mutant in 2 brothers]J L Dupond, B Mousson, F Guerber, et al.
Journal of the Neurological Sciences|March 1, 1996
Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cellsJ Villard, A Fischer, G Mandon, et al.
Annales De Biologie Clinique|January 1, 1995
Serum 5'-nucleotidase and alkaline phosphatase activities after high dose chemotherapy and bone marrow transplantation in cases of malignancy in childrenP Clerc-Renaud, G Souillet, C Lahet, 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.
Pageof 5