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C Marsac

Showing results (51-60 of 91) with videos related to

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European Neurology|January 1, 1991
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegiaH Reichmann, F Degoul, R Gold, et al.
The Journal of Pediatrics|December 1, 1993
Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathyC Marsac, D Stansbie, G Bonne, et al.
The Journal of Pediatrics|June 1, 1981
Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to ageJ M Saudubray, C Marsac, J M Limal, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Nucleic Acids Research|February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathiesF Degoul, I Nelson, S Amselem, 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.
Cancer Research|July 15, 1995
Impairment of the mitochondrial respiratory chain activity in diethylnitrosamine-induced rat hepatomas: possible involvement of oxygen free radicalsE Boitier, M Merad-Boudia, C Guguen-Guillouzo, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
European Neurology|January 1, 1991
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegiaH Reichmann, F Degoul, R Gold, et al.
The Journal of Pediatrics|December 1, 1993
Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathyC Marsac, D Stansbie, G Bonne, et al.
The Journal of Pediatrics|June 1, 1981
Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to ageJ M Saudubray, C Marsac, J M Limal, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Nucleic Acids Research|February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathiesF Degoul, I Nelson, S Amselem, 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.
Cancer Research|July 15, 1995
Impairment of the mitochondrial respiratory chain activity in diethylnitrosamine-induced rat hepatomas: possible involvement of oxygen free radicalsE Boitier, M Merad-Boudia, C Guguen-Guillouzo, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Pageof 10