AAAAAA
Results:
1-11
|
Results: 11
Authors:
de Lonlay, P
Valnot, I
Barrientos, A
Gorbatyuk, M
Tzagoloff, A
Taanman, JW
Benayoun, E
Chretien, D
Kadhom, N
Lombes, A
de Baulny, HO
Niaudet, P
Munnich, M
Rustin, P
Rotig, A
Citation: P. De Lonlay et al., A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure, NAT GENET, 29(1), 2001, pp. 57-60
Authors:
Legros, F
Chatzoglou, E
Frachon, P
de Baulny, HO
Laforet, P
Jardel, C
Godinot, C
Lombes, A
Citation: F. Legros et al., Functional characterization of novel mutations in the human cytochrome b gene, EUR J HUM G, 9(7), 2001, pp. 510-518
Authors:
Barthelemy, C
de Baulny, HO
Diaz, J
Cheval, MA
Frachon, P
Romero, N
Goutieres, F
Fardeau, M
Lombes, A
Citation: C. Barthelemy et al., Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation, ANN NEUROL, 49(5), 2001, pp. 607-617
Authors:
Gignoux, L
Maisonobe, T
Laforet, P
Lombes, A
Lyon-Caen, O
Fontaine, B
Citation: L. Gignoux et al., Mitochondrial cytopathy (MERRF) without ragged-red fibers, REV NEUROL, 157(4), 2001, pp. 427-429
Authors:
Bataillard, M
Chatzoglou, E
Rumbach, L
Sternberg, D
Tournade, A
Laforet, P
Jardel, C
Maisonobe, T
Lombes, A
Citation: M. Bataillard et al., Atypical MELAS syndrome associated with a new mitochondrial tRNA glutaminepoint mutation, NEUROLOGY, 56(3), 2001, pp. 405-407
Authors:
Hogrel, JY
Laforet, P
Ben Yaou, R
Chevrot, M
Eymard, B
Lombes, A
Citation: Jy. Hogrel et al., A non-ischemic forearm exercise test for the screening of patients with exercise intolerance, NEUROLOGY, 56(12), 2001, pp. 1733-1738
Authors:
Sternberg, D
Chatzoglou, E
Laforet, P
Fayet, G
Jardel, C
Blondy, P
Fardeau, M
Amselem, S
Eymard, B
Lombes, A
Citation: D. Sternberg et al., Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders, BRAIN, 124, 2001, pp. 984-994
Authors:
Laforet, P
Ziegler, F
Sternberg, D
Rouche, A
Frachon, P
Fardeau, M
Eymard, B
Lombes, A
Citation: P. Laforet et al., MELAS (A3243G) mutation of mitochondrial DNA: a study of the relationshipsbetween the clinical phenotype in 19 patients and morphological and molecular data., REV NEUROL, 156(12), 2000, pp. 1136-1147
Authors:
Bakker, A
Barthelemy, C
Frachon, P
Chateau, D
Sternberg, D
Mazat, JP
Lombes, A
Citation: A. Bakker et al., Functional mitochondrial heterogeneity in heteroplasmic cells carrying themitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes), PEDIAT RES, 48(2), 2000, pp. 143-150
Authors:
Chariot, P
Drogou, I
de Lacroix-Szmania, I
Eliezer-Vanerot, MC
Chazaud, B
Lombes, A
Schaeffer, A
Zafrani, ES
Citation: P. Chariot et al., Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion, J HEPATOL, 30(1), 1999, pp. 156-160
Authors:
Procaccio, V
Mousson, B
Beugnot, R
Duborjal, H
Feillet, F
Putet, G
Pignot-Paintrand, I
Lombes, A
De Coo, R
Smeets, H
Lunardi, J
Issartel, JP
Citation: V. Procaccio et al., Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts, J CLIN INV, 104(1), 1999, pp. 83-92
Risultati:
1-11
|