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Results: 1-25 | 26-30
Results: 1-25/30
Association between the NOS3 (-786 T/C) and the ACE (I/D) DNA genotypes and early coronary artery disease
Authors: Alvarez, R Gonzalez, P Batalla, A Reguero, JR Iglesias-Cubero, G Hevia, S Cortina, A Merino, E Gonzalez, I Alvarez, V Coto, E
Citation: R. Alvarez et al., Association between the NOS3 (-786 T/C) and the ACE (I/D) DNA genotypes and early coronary artery disease, NITRIC OXID, 5(4), 2001, pp. 343-348
P53 allelic loss and outcome in patients with squamous cell carcinoma of the head and neck
Authors: Rodrigo, JP Coto, E Gonzalez, MV Maldonado, M Suarez, C
Citation: Jp. Rodrigo et al., P53 allelic loss and outcome in patients with squamous cell carcinoma of the head and neck, EUR ARCH OT, 258(5), 2001, pp. 255-258
Apolipoprotein E genotype and coronary heart disease
Authors: Batalla, A Alvarez, R Hevia, S Reguero, JR Coto, E
Citation: A. Batalla et al., Apolipoprotein E genotype and coronary heart disease, J AM COL C, 37(1), 2001, pp. 329-330
Early-onset Parkinson's disease associated with a new parkin mutation in aSpanish family
Authors: Alvarez, V Guisasola, LM Moreira, VG Lahoz, CH Coto, E
Citation: V. Alvarez et al., Early-onset Parkinson's disease associated with a new parkin mutation in aSpanish family, NEUROSCI L, 313(1-2), 2001, pp. 108-110
ACE gene polimorphism and cardiovascular disease
Authors: Coto, E
Citation: E. Coto, ACE gene polimorphism and cardiovascular disease, NEFROLOGIA, 21, 2001, pp. 67-69
Lack of association between polymorphisms of the coagulation factor VII and myocardial infarction in middle-aged Spanish men
Authors: Batalla, A Alvarez, R Reguero, JR Gonzalez, P Alvarez, V Cubero, GI Cortina, A Coto, E
Citation: A. Batalla et al., Lack of association between polymorphisms of the coagulation factor VII and myocardial infarction in middle-aged Spanish men, INT J CARD, 80(2-3), 2001, pp. 209-212
Variation at the angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis
Authors: Coto, E Rodrigo, L Alvarez, R Fuentes, D Rodriguez, T Menendez, LG Ciriza, C Gonzalez, P Alvarez, V
Citation: E. Coto et al., Variation at the angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis, J CARDIO PH, 38(6), 2001, pp. 833-839
Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer disease
Authors: Sanchez, L Alvarez, V Gonzalez, P Gonzalez, I Alvarez, R Coto, E
Citation: L. Sanchez et al., Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer disease, AM J MED G, 105(1), 2001, pp. 76-78
Variability of genetic alterations in different sites of head and neck cancer
Authors: Rodrigo, JP Suarez, C Gonzalez, MV Lazo, PS Ramos, S Coto, E Alvarez, I Garcia, LA Martinet, JA
Citation: Jp. Rodrigo et al., Variability of genetic alterations in different sites of head and neck cancer, LARYNGOSCOP, 111(7), 2001, pp. 1297-1301
Genetic variation in the renin-angiotensin system and athletic performance
Authors: Alvarez, R Terrados, N Ortolano, R Iglesias-Cubero, G Reguero, JR Batalla, A Cortina, A Fernandez-Garcia, B Rodriguez, C Braga, S Alvarez, V Coto, E
Citation: R. Alvarez et al., Genetic variation in the renin-angiotensin system and athletic performance, EUR J A PHY, 82(1-2), 2000, pp. 117-120
Normal frequencies of the C677T genotypes on the methylenetetrahydrofolatereductase (MTHFR) gene among lymphoproliferative disorders but not in multiple myeloma
Authors: Ordonez, AJG Carreira, JMF Alvarez, CRF Martin, L Garcia, JS Rodriguez, JMM Alvarez, MV Coto, E
Citation: Ajg. Ordonez et al., Normal frequencies of the C677T genotypes on the methylenetetrahydrofolatereductase (MTHFR) gene among lymphoproliferative disorders but not in multiple myeloma, LEUK LYMPH, 39(5-6), 2000, pp. 607-612
Analysis of chromosome 6p in Spanish families with recessive polycystic kidney disease
Authors: Alvarez, V Malaga, S Navarro, M Espinosa, L Hidalgo, E Badia, J Alvarez, R Coto, E
Citation: V. Alvarez et al., Analysis of chromosome 6p in Spanish families with recessive polycystic kidney disease, PED NEPHROL, 14(3), 2000, pp. 205-207
Comparison of the risk of pulmonary embolism and deep vein thrombosis in the presence of factor V Leiden or prothrombin G20210A
Authors: Ordonez, AJG Carreira, JMF Alvarez, CRF Rodriguez, JMM Alvarez, MV Coto, E
Citation: Ajg. Ordonez et al., Comparison of the risk of pulmonary embolism and deep vein thrombosis in the presence of factor V Leiden or prothrombin G20210A, THROMB HAEM, 83(2), 2000, pp. 352-354
A DNA polymorphism at the alpha(2)-macroglobulin gene is associated with the severity of rheumatoid arthritis
Authors: Zapico, I Coto, E Rodriguez, A Alvarez, C Torre, JC Alvarez, V
Citation: I. Zapico et al., A DNA polymorphism at the alpha(2)-macroglobulin gene is associated with the severity of rheumatoid arthritis, J RHEUMATOL, 27(10), 2000, pp. 2308-2311
Genomic, farmacogenomic and medicine in the XXIst century
Authors: Coto, E
Citation: E. Coto, Genomic, farmacogenomic and medicine in the XXIst century, NEFROLOGIA, 20(3), 2000, pp. 209-213
Location of mutations within the PKD2 gene influences clinical outcome
Authors: Hateboer, N Veldhuisen, B Peters, D Breuning, MH San-Millan, JL Bogdanova, N Coto, E von Dijk, MA Afzal, AR Jeffery, S Saggar-Malik, AK Torra, R Dimitrakov, D Martinez, I de Castro, SS Krawczak, M Ravine, D
Citation: N. Hateboer et al., Location of mutations within the PKD2 gene influences clinical outcome, KIDNEY INT, 57(4), 2000, pp. 1444-1451
Hyperlipidaemia and glycoprotein IIIa polymorphisms
Authors: Batalla, A Reguero, JR Cubero, GI Coto, E
Citation: A. Batalla et al., Hyperlipidaemia and glycoprotein IIIa polymorphisms, MED CLIN, 114(2), 2000, pp. 77-77
Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction
Authors: Batalla, A Alvarez, R Reguero, JR Hevia, S Iglesias-Cubero, G Alvarez, V Cortina, A Gonzalez, P Celada, MM Medina, A Coto, E
Citation: A. Batalla et al., Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction, CLIN CHEM, 46(12), 2000, pp. 1910-1915
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease
Authors: Reynolds, DM Hayashi, T Cai, YQ Veldhuisen, B Watnick, TJ Lens, XM Mochizuki, T Qian, F Maeda, Y Li, L Fossdal, R Coto, E Wu, GQ Breuning, MH Germino, GG Peters, DJM Somlo, S
Citation: Dm. Reynolds et al., Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease, J AM S NEPH, 10(11), 1999, pp. 2342-2351
The O blood group protects against venous thromboembolism in individuals with the factor V Leiden but not the prothrombin (factor II G20210A) mutation
Authors: Ordonez, AJG Rodriguez, JMM Martin, L Alvarez, V Coto, E
Citation: Ajg. Ordonez et al., The O blood group protects against venous thromboembolism in individuals with the factor V Leiden but not the prothrombin (factor II G20210A) mutation, BL COAG FIB, 10(5), 1999, pp. 303-307
The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease
Authors: Vargas, M Soto, I Pinto, CR Urgelles, MF Batalla, A Rodriguez-Reguero, J Cortina, A Alvarez, V Coto, E
Citation: M. Vargas et al., The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease, BL COAG FIB, 10(1), 1999, pp. 39-41
Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop)
Authors: Valdes, N de Nanclares, GP Alvarez, V Castano, L Diaz-Cadorniga, F Aller, J Coto, E
Citation: N. Valdes et al., Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop), CLIN ENDOCR, 50(3), 1999, pp. 309-313
Comparison of phenotypes of polycystic kidney disease types 1 and 2
Authors: Hateboer, N Dijk, MAV Bogdanova, N Coto, E Saggar-Malik, AK San Millan, JL Torra, R Breuning, M Ravine, D
Citation: N. Hateboer et al., Comparison of phenotypes of polycystic kidney disease types 1 and 2, LANCET, 353(9147), 1999, pp. 103-107
N-acetyltransferase-2, glutathione S-transferase M1, alcohol dehydrogenase, and cytochrome P450IIE1 genotypes in alcoholic liver cirrhosis: A case-control study
Authors: Rodrigo, L Alvarez, V Rodriguez, M Perez, R Alvarez, R Coto, E
Citation: L. Rodrigo et al., N-acetyltransferase-2, glutathione S-transferase M1, alcohol dehydrogenase, and cytochrome P450IIE1 genotypes in alcoholic liver cirrhosis: A case-control study, SC J GASTR, 34(3), 1999, pp. 303-307
Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain)
Authors: Alvarez, V Alvarez, R Pena, J Lahoz, CH Martinez, C Menendez-Guisasola, L Salas-Puig, J Moris, G Uria, D Menes, BB Ribacoba, R Vidal, JA Coto, E
Citation: V. Alvarez et al., Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain), MED CLIN, 113(12), 1999, pp. 441-443
Risultati: 1-25 | 26-30