Degoul F - Search Results

1

[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: degoul f. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

2

Uneven distribution of mitochondrial DNA mutation in MERRF dizygotic twins.

Penisson-Besnier I, Degoul F, Desnuelle C, Dubas F, Josi K, Emile J, Lestienne P. Penisson-Besnier I, et al. Among authors: degoul f. J Neurol Sci. 1992 Jul;110(1-2):144-8. doi: 10.1016/0022-510x(92)90021-c. J Neurol Sci. 1992. PMID: 1324294

3

Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations.

Nelson I, Bonne G, Degoul F, Marsac C, Ponsot G, Lestienne P. Nelson I, et al. Among authors: degoul f. Neuropediatrics. 1992 Aug;23(4):199-205. doi: 10.1055/s-2008-1071341. Neuropediatrics. 1992. PMID: 1407387

4

Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.

Reichmann H, Degoul F, Gold R, Meurers B, Ketelsen UP, Hartmann J, Marsac C, Lestienne P. Reichmann H, et al. Among authors: degoul f. Eur Neurol. 1991;31(2):108-13. doi: 10.1159/000116656. Eur Neurol. 1991. PMID: 1646110

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

6

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: degoul f. Dig Dis Sci. 1992 Mar;37(3):456-63. doi: 10.1007/BF01307743. Dig Dis Sci. 1992. PMID: 1735370

7

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. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

8

Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunction.

Mhiri C, Baudrimont M, Bonne G, Geny C, Degoul F, Marsac C, Roullet E, Gherardi R. Mhiri C, et al. Among authors: degoul f. Ann Neurol. 1991 Jun;29(6):606-14. doi: 10.1002/ana.410290607. Ann Neurol. 1991. PMID: 1892364

9

Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies.

Degoul F, Nelson I, Amselem S, Romero N, Obermaier-Kusser B, Ponsot G, Marsac C, Lestienne P. Degoul F, et al. Nucleic Acids Res. 1991 Feb 11;19(3):493-6. doi: 10.1093/nar/19.3.493. Nucleic Acids Res. 1991. PMID: 2011523 Free PMC article.

10

Identification of point mutations by mispairing PCR as exemplified in MERRF disease.

Seibel P, Degoul F, Romero N, Marsac C, Kadenbach B. Seibel P, et al. Among authors: degoul f. Biochem Biophys Res Commun. 1990 Dec 14;173(2):561-5. doi: 10.1016/s0006-291x(05)80071-3. Biochem Biophys Res Commun. 1990. PMID: 2124485

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