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Results: 5

Authors: BOITIER E DEGOUL F DESGUERRE I CHARPENTIER C FRANCOIS D PONSOT G DIRY M RUSTIN P MARSAC C
Citation: E. Boitier et al., A CASE OF MITOCHONDRIAL ENCEPHALOMYOPATHY ASSOCIATED WITH A MUSCLE COENZYME Q(10) DEFICIENCY, Journal of the neurological sciences, 156(1), 1998, pp. 41-46

Authors: MARSAC C BENELLI C DESGUERRE I DIRY M FOUQUE F DEMEIRLEIR L PONSOT G SENECA S POGGI F SAUDUBRAY JM ZABOT MT FONTAN D LISSENS W
Citation: C. Marsac et al., BIOCHEMICAL-STUDIES AND GENETIC-STUDIES OF 4 PATIENTS WITH PYRUVATE-DEHYDROGENASE-E1-ALPHA DEFICIENCY, Human genetics, 99(6), 1997, pp. 785-792

Authors: DEGOUL F FRANCOIS D DIRY M PONSOT G DESGUERRE I HERON B MARSAC C MOUTARD ML
Citation: F. Degoul et al., A NEAR HOMOPLASMIC T8993G MTDNA MUTATION IN A PATIENT WITH ATYPIC LEIGH-SYNDROME NOT PRESENT IN THE MOTHERS TISSUES, Journal of inherited metabolic disease, 20(1), 1997, pp. 49-53

Authors: DEGOUL F DIRY M RODRIGUEZ D ROBAIN O FRANCOIS D PONSOT G MARSAC C DESGUERRE I
Citation: F. Degoul et al., CLINICAL, BIOCHEMICAL, AND MOLECULAR ANALYSIS OF A MATERNALLY INHERITED CASE OF LEIGH-SYNDROME (MILS) ASSOCIATED WITH THE MTDNA T8993G POINT MUTATION, Journal of inherited metabolic disease, 18(6), 1995, pp. 682-688

Authors: DEGOUL F DIRY M POUSERRADELL A LLORETA J MARSAC C
Citation: F. Degoul et al., MYO-LEUKOENCEPHALOPATHY IN TWINS - STUDY OF 3243-MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES MITOCHONDRIAL-DNA MUTATION, Annals of neurology, 35(3), 1994, pp. 365-370
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