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Results: 1-25/53
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:
Castro-Gago, M
Pintos-Martinez, E
Forteza-Vila, J
Iglesias-Diz, M
Ucieda-Somoza, R
Silva-Villar, I
Codesido-Lopez, J
Viso-Lorenzo, A
Campos, Y
Arenas, J
Eiris-Punal, J
Citation: M. Castro-gago et al., Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction, J CHILD NEU, 16(11), 2001, pp. 858-862
Authors:
Bertran, C
Arenas, J
Parra, O
Citation: C. Bertran et al., Macrofauna of the lower reach and estuary of Biobio river (Chile): changesassociated to seasonal changes of the river flow, REV CHIL HN, 74(2), 2001, pp. 331-340
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:
Juma, C
Fang, K
Honca, D
Huete-Perez, J
Konde, V
Lee, SH
Arenas, J
Ivinson, A
Robinson, H
Singh, S
Citation: C. Juma et al., Global governance of technology: meeting the needs of developing countries[1], INT J TEC M, 22(7-8), 2001, pp. 629-655
Authors:
Nicolas, J
Toval, A
Arenas, J
Alcalde, J
Citation: J. Nicolas et al., Formal validation and verification of atomic resolution microscope controland topography, CYBERN SYST, 32(8), 2001, pp. 851-870
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:
Martinez-Fernandez, E
Gil-Peralta, A
Garcia-Lozano, R
Chinchon, I
Aguilera, I
Fernandez-Lopez, O
Arenas, J
Campos, Y
Bautista, J
Citation: E. Martinez-fernandez et al., Mitochondrial disease and stroke, STROKE, 32(11), 2001, pp. 2507-2510
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:
Aguilera, I
Garcia-Lozano, JR
Munoz, A
Arenas, J
Campos, Y
Chinchon, I
Roldan, AN
Bautista, J
Citation: I. Aguilera et al., Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease, J NEUR SCI, 192(1-2), 2001, pp. 81-84
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:
Arenas, J
Alonso, S
Latorre, FF
Citation: J. Arenas et al., Spiral CT diagnosis of isolated systemic supply to normal lung merging from the coeliac trunk, CLIN RADIOL, 56(2), 2001, pp. 163-165
Authors:
Martin, MA
Rubio, JC
Garcia, A
Fernandez, MA
Campos, Y
Krawczak, M
Cooper, DN
Arenas, J
Citation: Ma. Martin et al., Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease, CLIN GENET, 59(1), 2001, pp. 48-51
Authors:
Fernandez-Moreno, MA
Bornstein, B
Campos, Y
Arenas, J
Garesse, R
Citation: Ma. Fernandez-moreno et al., The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes, MOL GEN MET, 70(3), 2000, pp. 238-240
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:
Martin, MA
Rubio, JC
Campos, Y
Ricoy, JR
Cabello, A
Arenas, J
Citation: Ma. Martin et al., A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's disease, NEUROMUSC D, 10(6), 2000, pp. 447-449
Authors:
Rubio, JC
Martin, MA
Campos, Y
Cabello, A
Arenas, J
Citation: Jc. Rubio et al., A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease, NEUROMUSC D, 10(2), 2000, pp. 138-140
Authors:
Campos, Y
Martin, MA
Caballero, C
Rubio, JC
de la Cruz, F
Tunon, T
Arenas, J
Citation: Y. Campos et al., Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction, NEUROMUSC D, 10(1), 2000, pp. 56-58
Authors:
Rodriguez-Benitez, P
Perez-Garcia, R
Arenas, J
Valderrabano, F
Citation: P. Rodriguez-benitez et al., L-carnitine in dialysis, more than a commercial affair, NEPH DIAL T, 15(9), 2000, pp. 1477-1478
Authors:
Martin, MA
Gomez, MA
Guillen, F
Bornstein, B
Campos, Y
Rubio, JC
de la Calzada, CS
Arenas, J
Citation: Ma. Martin et al., Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure, BBA-MOL BAS, 1502(3), 2000, pp. 330-336
Authors:
Gil, S
de la Iglesia, P
Verdu, JF
de Espana, F
Arenas, J
Irurzun, J
Citation: S. Gil et al., Effectiveness and safety of balloon dilation of the papilla and the use ofan occlusion balloon for clearance of bile duct calculi, AM J ROENTG, 174(5), 2000, pp. 1455-1460
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:
Jimenez-Jimenez, FJ
Molina, JA
Vargas, C
Gomez, P
de Bustos, F
Zurdo, M
Gomez-Escalonilla, C
Barcenilla, B
Berbel, A
Camacho, A
Arenas, J
Citation: Fj. Jimenez-jimenez et al., Normal cerebrospinal fluid levels of insulin in patients with Parkinson's disease, J NEURAL TR, 107(4), 2000, pp. 445-449
Authors:
Jimenez-Jimenez, FJ
Molina, JA
de Bustos, F
Garcia-Redondo, A
Gomez-Escalonilla, C
Martinez-Salio, A
Berbel, A
Camacho, A
Zurdo, M
Barcenilla, B
de Salamanca, RE
Arenas, J
Citation: Fj. Jimenez-jimenez et al., Serum levels of coenzyme Q(10) in patients with Parkinson's disease, J NEURAL TR, 107(2), 2000, pp. 177-181