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F Degoul

Showing results (11-20 of 27) with videos related to

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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.
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.
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.
Gastroenterology|April 21, 2001
Homozygosity for alanine in the mitochondrial targeting sequence of superoxide dismutase and risk for severe alcoholic liver diseaseF Degoul, A Sutton, A Mansouri, 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.
British Journal of Cancer|May 9, 2007
N-(4-iodophenyl)-N'-(2-chloroethyl)urea as a microtubule disrupter: in vitro and in vivo profiling of antitumoral activity on CT-26 murine colon carcinoma cell line cultured and grafted to miceM Borel, F Degoul, Y Communal, et al.
Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
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.
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.
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.
Gastroenterology|April 21, 2001
Homozygosity for alanine in the mitochondrial targeting sequence of superoxide dismutase and risk for severe alcoholic liver diseaseF Degoul, A Sutton, A Mansouri, 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.
British Journal of Cancer|May 9, 2007
N-(4-iodophenyl)-N'-(2-chloroethyl)urea as a microtubule disrupter: in vitro and in vivo profiling of antitumoral activity on CT-26 murine colon carcinoma cell line cultured and grafted to miceM Borel, F Degoul, Y Communal, et al.
Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Pageof 3