François D - Search Results

1

Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.

Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M. Romero NB, et al. Among authors: francois d. J Neurol Sci. 1989 Nov;93(2-3):297-309. doi: 10.1016/0022-510x(89)90199-8. J Neurol Sci. 1989. PMID: 2556504

2

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: francois d. J Neurol Sci. 1991 Oct;105(2):217-24. doi: 10.1016/0022-510x(91)90148-z. J Neurol Sci. 1991. PMID: 1661776

3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M, et al. Degoul F, et al. Among authors: francois d. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

[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. Among authors: francois d. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

5

A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency.

Boitier E, Degoul F, Desguerre I, Charpentier C, François D, Ponsot G, Diry M, Rustin P, Marsac C. Boitier E, et al. Among authors: francois d. J Neurol Sci. 1998;156(1):41-6. doi: 10.1016/s0022-510x(98)00006-9. J Neurol Sci. 1998. PMID: 9559985

6

Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutation.

Degoul F, Diry M, Rodriguez D, Robain O, Francois D, Ponsot G, Marsac C, Desguerre I. Degoul F, et al. Among authors: francois d. J Inherit Metab Dis. 1995;18(6):682-8. doi: 10.1007/BF02436757. J Inherit Metab Dis. 1995. PMID: 8750605

7

Impairment of mitochondrial 5-aminolevulinic acid synthase activity in Gunn rat liver.

Celier C, Francois D, Marsac C, Cresteil T. Celier C, et al. Among authors: francois d. Biochem Pharmacol. 1992 Oct 6;44(7):1465-7. doi: 10.1016/0006-2952(92)90550-3. Biochem Pharmacol. 1992. PMID: 1417967

8

A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.

Degoul F, François D, Diry M, Ponsot G, Desguerre I, Héron B, Marsac C, Moutard ML. Degoul F, et al. Among authors: francois d. J Inherit Metab Dis. 1997 Mar;20(1):49-53. doi: 10.1023/a:1005357506614. J Inherit Metab Dis. 1997. PMID: 9061567

9

Mitochondria are selective targets for the protective effects of heat shock against oxidative injury.

Polla BS, Kantengwa S, François D, Salvioli S, Franceschi C, Marsac C, Cossarizza A. Polla BS, et al. Among authors: francois d. Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6458-63. doi: 10.1073/pnas.93.13.6458. Proc Natl Acad Sci U S A. 1996. PMID: 8692837 Free PMC article.

10

Evidence of mitochondrial impairment during cardiac allograft rejection.

Duboc D, Abastado P, Muffat-Joly M, Perrier P, Toussaint M, Marsac C, Francois D, Lavergne T, Pocidalo JJ, Guerin F, et al. Duboc D, et al. Among authors: francois d. Transplantation. 1990 Nov;50(5):751-5. Transplantation. 1990. PMID: 2238049

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