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Results:
1-10
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Results: 10
Authors:
Campos, Y
Gamez, J
Garcia, A
Andreu, AL
Rubio, JC
Martin, MA
del Hoyo, P
Navarro, C
Cervera, C
Garesse, R
Arenas, J
Citation: Y. Campos et al., A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy, NEUROMUSC D, 11(5), 2001, pp. 477-480
Authors:
Martin, MA
Rubio, JC
Buchbinder, J
Fernandez-Hojas, R
del Hoyo, P
Teijeira, S
Gamez, J
Navarro, C
Fernandez, JM
Cabello, A
Campos, Y
Cervera, C
Culebras, JM
Andreu, AL
Fletterick, R
Arenas, J
Citation: Ma. Martin et al., Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): A genotype-phenotype correlation study, ANN NEUROL, 50(5), 2001, pp. 574-581
Authors:
Campos, Y
Garcia-Redondo, A
Fernandez-Moreno, MA
Martinez-Pardo, M
Goda, G
Rubio, JC
Martin, MA
del Hoyo, P
Cabello, A
Bornstein, B
Garesse, R
Arenas, J
Citation: Y. Campos et al., Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome c oxidase II gene, ANN NEUROL, 50(3), 2001, pp. 409-413
Authors:
Campos, Y
Garcia, A
Eiris, J
Fuster, M
Rubio, JC
Martin, MA
del Hoyo, P
Pintos, E
Castro-Gago, M
Arenas, J
Citation: Y. Campos et al., Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation, J INH MET D, 24(6), 2001, pp. 685-687
Authors:
de la Pena, P
Bornstein, B
del Hoyo, P
Fernandez-Moreno, MA
Martin, MA
Campos, Y
Gomez-Escalonilla, C
Molina, JA
Cabello, A
Arenas, J
Garesse, R
Citation: P. De La Pena et al., Mitochondrial dysfunction associated with a mutation in the Notch3 gene ina CADASIL family, NEUROLOGY, 57(7), 2001, pp. 1235-1238
Authors:
Martinez, B
del Hoyo, P
Martin, MA
Arenas, J
Perez-Castillo, A
Santos, A
Citation: B. Martinez et al., Thyroid hormone regulates oxidative phosphorylation in the cerebral cortexand striatum of neonatal rats, J NEUROCHEM, 78(5), 2001, pp. 1054-1063
Authors:
Campos, Y
Lorenzo, G
Martin, MA
Torregrosa, A
del Hoyo, P
Rubio, JC
Garcia, A
Arenas, J
Citation: Y. Campos et al., A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes, NEUROMUSC D, 10(7), 2000, pp. 493-496
Authors:
Molina, JA
de Bustos, F
Jimenez-Jimenez, FJ
Gomez-Escalonilla, C
Garcia-Redondo, A
Esteban, J
Guerrero-Sola, G
del Hoyo, P
Martinez-Salio, A
Ramirez-Ramos, C
Indurain, GR
Arenas, J
Citation: Ja. Molina et al., Serum levels of coenzyme Q(10) in patients with amyotrophic lateral sclerosis, J NEURAL TR, 107(8-9), 2000, pp. 1021-1026
Authors:
de Bustos, F
Jimenez-Jimenez, FJ
Molina, JA
Gomez-Escalonilla, C
de Andres, C
del Hoyo, P
Zurdo, M
Tallon-Barranco, A
Berbel, A
Porta-Etessam, J
Parrilla, G
Arenas, J
Citation: F. De Bustos et al., Serum levels of coenzyme Q(10) in patients with multiple sclerosis, ACT NEUR SC, 101(3), 2000, pp. 209-211
Authors:
Campos, Y
Martin, MA
Garcia-Silva, T
del Hoyo, P
Rubio, JC
Castro-Gago, M
Garcia-Penas, J
Casas, J
Cabello, A
Ricoy, JR
Arenas, J
Citation: Y. Campos et al., Clinical heterogeneity associated with mitochondrial DNA depletion in muscle, NEUROMUSC D, 8(8), 1998, pp. 568-573
Risultati:
1-10
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