Marsac C - Search Results

1

[Familial mitochondrial encephalopathy. A clinicopathologic study].

Estournet B, Duyckaerts C, Marsac C, Chabbi N, Bataille J, Barois A, Hauw JJ, Goulon M. Estournet B, et al. Among authors: marsac c. Rev Neurol (Paris). 1991;147(6-7):491-6. Rev Neurol (Paris). 1991. PMID: 1660181 French.

2

[Clinical and electrophysiologic study of the peripheral nerve in 28 cases of mitochondrial disease].

Eymard B, Penicaud A, Leger JM, Romero N, Marsac C, Fardeau M, Brunet P. Eymard B, et al. Among authors: marsac c. Rev Neurol (Paris). 1991;147(6-7):508-12. Rev Neurol (Paris). 1991. PMID: 1660183 French.

3

[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy].

Marsac C, Degoul F, Bonne G, Romero N, Nelson I, Fardeau M, François D, Ponsot G, Harpey JP, Eymard B, et al. Marsac C, et al. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

4

[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin].

Pinard JM, Marsac C, Barkaoui E, Desguerre I, Birch-Machin M, Reinert P, Ponsot G. Pinard JM, et al. Among authors: marsac c. Arch Pediatr. 1999 Apr;6(4):421-6. doi: 10.1016/s0929-693x(99)80224-3. Arch Pediatr. 1999. PMID: 10230482 French.

5

Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF).

Seibel P, Degoul F, Bonne G, Romero N, François D, Paturneau-Jouas M, Ziegler F, Eymard B, Fardeau M, Marsac C, et al. Seibel P, et al. Among authors: marsac c. J Neurol Sci. 1991 Oct;105(2):217-24. doi: 10.1016/0022-510x(91)90148-z. J Neurol Sci. 1991. PMID: 1661776

6

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.

7

Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathy.

Chariot P, Bonne G, Authier FJ, Marsac C, Gherardi R. Chariot P, et al. Among authors: marsac c. J Neurol Sci. 1994 Sep;125(2):190-3. doi: 10.1016/0022-510x(94)90034-5. J Neurol Sci. 1994. PMID: 7807166

8

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.

Bénit P, Slama A, Cartault F, Giurgea I, Chretien D, Lebon S, Marsac C, Munnich A, Rötig A, Rustin P. Bénit P, et al. Among authors: marsac c. J Med Genet. 2004 Jan;41(1):14-7. doi: 10.1136/jmg.2003.014316. J Med Genet. 2004. PMID: 14729820 Free PMC article.

9

Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation.

Desguerre I, Pinton F, Nabbout R, Moutard ML, N'Guyen S, Marsac C, Ponsot G, Dulac O. Desguerre I, et al. Among authors: marsac c. Neuropediatrics. 2003 Jun;34(5):265-9. doi: 10.1055/s-2003-43258. Neuropediatrics. 2003. PMID: 14598233

10

Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorder.

Li V, Hostein J, Romero NB, Marsac C, Mezin P, Bost R, Degoul F, Fardeau M, Fournet J. Li V, et al. Among authors: marsac c. Dig Dis Sci. 1992 Mar;37(3):456-63. doi: 10.1007/BF01307743. Dig Dis Sci. 1992. PMID: 1735370

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