Marsac C - Search Results

1

Blood mononuclear cells energy metabolism response to muscular exercise.

Ferry A, Marsac C, Duvallet A, Rieu M. Ferry A, et al. Among authors: marsac c. J Sports Med Phys Fitness. 1991 Jun;31(2):208-12. J Sports Med Phys Fitness. 1991. PMID: 1661353

2

Expression of human cytochrome c oxidase subunits during fetal development.

Bonne G, Seibel P, Possekel S, Marsac C, Kadenbach B. Bonne G, et al. Among authors: marsac c. Eur J Biochem. 1993 Nov 1;217(3):1099-107. doi: 10.1111/j.1432-1033.1993.tb18342.x. Eur J Biochem. 1993. PMID: 8223633 Free article.

3

Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency.

Romero NB, Marsac C, Paturneau-Jouas M, Ogier H, Magnier S, Fardeau M. Romero NB, et al. Among authors: marsac c. Neuromuscul Disord. 1993 Jan;3(1):31-42. doi: 10.1016/0960-8966(93)90039-m. Neuromuscul Disord. 1993. PMID: 8392409 Review.

4

Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathy.

Marsac C, Stansbie D, Bonne G, Cousin J, Jehenson P, Benelli C, Leroux JP, Lindsay G. Marsac C, et al. J Pediatr. 1993 Dec;123(6):915-20. doi: 10.1016/s0022-3476(05)80387-7. J Pediatr. 1993. PMID: 8229524

5

Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle.

Romero N, Marsac C, Fardeau M, Droste M, Schneyder B, Kadenbach B. Romero N, et al. Among authors: marsac c. Histochemistry. 1990;94(2):211-5. doi: 10.1007/BF02440190. Histochemistry. 1990. PMID: 2162812

6

Differential effect of DCA treatment on the pyruvate dehydrogenase complex in patients with severe PDHC deficiency.

Fouque F, Brivet M, Boutron A, Vequaud C, Marsac C, Zabot MT, Benelli C. Fouque F, et al. Among authors: marsac c. Pediatr Res. 2003 May;53(5):793-9. doi: 10.1203/01.PDR.0000057987.46622.64. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621116

7

Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.

Birch-Machin MA, Marsac C, Ponsot G, Parfait B, Taylor RW, Rustin P, Munnich A. Birch-Machin MA, et al. Among authors: marsac c. Biochem Biophys Res Commun. 1996 Mar 7;220(1):57-62. doi: 10.1006/bbrc.1996.0356. Biochem Biophys Res Commun. 1996. PMID: 8602857

8

A new case of pyruvate dehydrogenase deficiency due to a novel mutation in the PDX1 gene.

Dey R, Mine M, Desguerre I, Slama A, Van Den Berghe L, Brivet M, Aral B, Marsac C. Dey R, et al. Among authors: marsac c. Ann Neurol. 2003 Feb;53(2):273-7. doi: 10.1002/ana.10478. Ann Neurol. 2003. PMID: 12557299

9

Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis.

Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C. Aral B, et al. Among authors: marsac c. Am J Hum Genet. 1997 Dec;61(6):1318-26. doi: 10.1086/301653. Am J Hum Genet. 1997. PMID: 9399911 Free PMC article. Review.

10

A novel Y243S mutation in the pyruvate dehydrogenase El alpha gene subunit: correlation with thiamine pyrophosphate interaction.

Benelli C, Fouque F, Redonnet-Vernhet I, Malgat M, Fontan D, Marsac C, Dey R. Benelli C, et al. Among authors: marsac c. J Inherit Metab Dis. 2002 Aug;25(4):325-7. doi: 10.1023/a:1016570828778. J Inherit Metab Dis. 2002. PMID: 12227466

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