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    1. Alvarez, R; Gonzalez, P; Batalla, A; Reguero, JR; Iglesias-Cubero, G; Hevia, S; Cortina, A; Merino, E; Gonzalez, I; Alvarez, V; Coto, E
      Association between the NOS3 (-786 T/C) and the ACE (I/D) DNA genotypes and early coronary artery disease

      NITRIC OXIDE-BIOLOGY AND CHEMISTRY
    2. Rodrigo, JP; Coto, E; Gonzalez, MV; Maldonado, M; Suarez, C
      P53 allelic loss and outcome in patients with squamous cell carcinoma of the head and neck

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    3. Batalla, A; Alvarez, R; Hevia, S; Reguero, JR; Coto, E
      Apolipoprotein E genotype and coronary heart disease

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    4. Alvarez, V; Guisasola, LM; Moreira, VG; Lahoz, CH; Coto, E
      Early-onset Parkinson's disease associated with a new parkin mutation in aSpanish family

      NEUROSCIENCE LETTERS
    5. Coto, E
      ACE gene polimorphism and cardiovascular disease

      NEFROLOGIA
    6. Batalla, A; Alvarez, R; Reguero, JR; Gonzalez, P; Alvarez, V; Cubero, GI; Cortina, A; Coto, E
      Lack of association between polymorphisms of the coagulation factor VII and myocardial infarction in middle-aged Spanish men

      INTERNATIONAL JOURNAL OF CARDIOLOGY
    7. Coto, E; Rodrigo, L; Alvarez, R; Fuentes, D; Rodriguez, T; Menendez, LG; Ciriza, C; Gonzalez, P; Alvarez, V
      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

      JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
    8. Sanchez, L; Alvarez, V; Gonzalez, P; Gonzalez, I; Alvarez, R; Coto, E
      Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Rodrigo, JP; Suarez, C; Gonzalez, MV; Lazo, PS; Ramos, S; Coto, E; Alvarez, I; Garcia, LA; Martinet, JA
      Variability of genetic alterations in different sites of head and neck cancer

      LARYNGOSCOPE
    10. 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
      Genetic variation in the renin-angiotensin system and athletic performance

      EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
    11. Ordonez, AJG; Carreira, JMF; Alvarez, CRF; Martin, L; Garcia, JS; Rodriguez, JMM; Alvarez, MV; Coto, E
      Normal frequencies of the C677T genotypes on the methylenetetrahydrofolatereductase (MTHFR) gene among lymphoproliferative disorders but not in multiple myeloma

      LEUKEMIA & LYMPHOMA
    12. Alvarez, V; Malaga, S; Navarro, M; Espinosa, L; Hidalgo, E; Badia, J; Alvarez, R; Coto, E
      Analysis of chromosome 6p in Spanish families with recessive polycystic kidney disease

      PEDIATRIC NEPHROLOGY
    13. Ordonez, AJG; Carreira, JMF; Alvarez, CRF; Rodriguez, JMM; Alvarez, MV; Coto, E
      Comparison of the risk of pulmonary embolism and deep vein thrombosis in the presence of factor V Leiden or prothrombin G20210A

      THROMBOSIS AND HAEMOSTASIS
    14. Zapico, I; Coto, E; Rodriguez, A; Alvarez, C; Torre, JC; Alvarez, V
      A DNA polymorphism at the alpha(2)-macroglobulin gene is associated with the severity of rheumatoid arthritis

      JOURNAL OF RHEUMATOLOGY
    15. Ezama-Coto, E; Fontanil-Gomez, Y; Galvan-Fernandez, S; Rodriguez-Blanco, C; Toribios-Alvarez, A
      New doors in Psychotherapy interviews: an exploration on delegate stages in the search of solutions

      PSICOTHEMA
    16. Coto, E
      Genomic, farmacogenomic and medicine in the XXIst century

      NEFROLOGIA
    17. 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
      Location of mutations within the PKD2 gene influences clinical outcome

      KIDNEY INTERNATIONAL
    18. Batalla, A; Reguero, JR; Cubero, GI; Coto, E
      Hyperlipidaemia and glycoprotein IIIa polymorphisms

      MEDICINA CLINICA
    19. Batalla, A; Alvarez, R; Reguero, JR; Hevia, S; Iglesias-Cubero, G; Alvarez, V; Cortina, A; Gonzalez, P; Celada, MM; Medina, A; Coto, E
      Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction

      CLINICAL CHEMISTRY
    20. 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
      Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    21. Ordonez, AJG; Rodriguez, JMM; Martin, L; Alvarez, V; Coto, E
      The O blood group protects against venous thromboembolism in individuals with the factor V Leiden but not the prothrombin (factor II G20210A) mutation

      BLOOD COAGULATION & FIBRINOLYSIS
    22. Vargas, M; Soto, I; Pinto, CR; Urgelles, MF; Batalla, A; Rodriguez-Reguero, J; Cortina, A; Alvarez, V; Coto, E
      The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease

      BLOOD COAGULATION & FIBRINOLYSIS
    23. Valdes, N; de Nanclares, GP; Alvarez, V; Castano, L; Diaz-Cadorniga, F; Aller, J; Coto, E
      Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop)

      CLINICAL ENDOCRINOLOGY
    24. Hateboer, N; Dijk, MAV; Bogdanova, N; Coto, E; Saggar-Malik, AK; San Millan, JL; Torra, R; Breuning, M; Ravine, D
      Comparison of phenotypes of polycystic kidney disease types 1 and 2

      LANCET
    25. Rodrigo, L; Alvarez, V; Rodriguez, M; Perez, R; Alvarez, R; Coto, E
      N-acetyltransferase-2, glutathione S-transferase M1, alcohol dehydrogenase, and cytochrome P450IIE1 genotypes in alcoholic liver cirrhosis: A case-control study

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    26. 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
      Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain)

      MEDICINA CLINICA
    27. Alvarez, R; Alvarez, V; Lahoz, CH; Martinez, C; Pena, J; Sanchez, JM; Guisasola, LM; Salas-Puig, J; Moris, G; Vidal, JA; Ribacoba, R; Menes, BB; Uria, D; Coto, E
      Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    28. Batalla, A; Reguero, JR; Cubero, GI; Coto, E
      Platelet glycoprotein IIIa polymorphisms, plasma lipo-protein(a) concentration and early coronary disease

      ATHEROSCLEROSIS
    29. Batalla, A; Reguero, JR; Cubero, CI; Coto, E
      Prothrombotic genetic risk factors and myocardial infarction at young age

      BLOOD
    30. Alvarez, V; Alvarez, R; Lahoz, CH; Martinez, C; Pena, J; Guisasola, LM; Salas-Puig, J; Moris, G; Uria, D; Menes, BB; Ribacoba, R; Vidal, JA; Sanchez, JM; Coto, E
      Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's disease

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    31. VARGA M; SOTO I; PINTO CR; URGELLES MF; COTO E
      MILD HYPERHOMOCYSTEINEMIA AND MTHFR C677T DO NOT INCREASE THE RISK FOR VENOUS THROMBOSIS IN A SPANISH POPULATION

      Blood coagulation & fibrinolysis
    32. ALVAREZ V; LOPEZLARREA C; COTO E
      MUTATIONAL ANALYSIS OF THE CCR5 AND CXCR4 GENES (HIV-1 CO-RECEPTORS) IN RESISTANCE TO HIV-1 INFECTION AND AIDS DEVELOPMENT AMONG INTRAVENOUS-DRUG-USERS

      Human genetics
    33. VALDES N; ALVAREZ V; DIAZCADORNIGA F; ALLER J; VILLAZON F; GARCIA I; HERRERO A; COTO E
      MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1) - LOH STUDIES IN A AFFECTED FAMILY AND IN SPORADIC CASES

      Anticancer research
    34. ARIZA M; ALVAREZ V; DECASTRO SS; PECES R; AGUADO S; ALVAREZ J; ARIAS M; ORTEGA F; MENENDEZ MJ; COTO E
      MUTATION ANALYSIS OF THE PKD1 GENE IN PATIENTS WITH ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE

      Nefrologia
    35. GONZALEZ MV; PELLO MF; ABLANEDO P; SUAREZ C; ALVAREZ V; COTO E
      CHROMOSOME 3P LOSS OF HETEROZYGOSITY AND MUTATION ANALYSIS OF THE FHIT AND BETA-CAT GENES IN SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK

      Journal of Clinical Pathology
    36. GONZALEZ MV; ALVAREZ V; PELLO MF; MENENDEZ MJ; SUAREZ C; COTO E
      GENETIC-POLYMORPHISM OF N-ACETYLTRANSFERASE-2, GLUTATHIONE S-TRANSFERASE-M1, AND CYTOCHROMES P450IIE1 AND P450IID6 IN THE SUSCEPTIBILITY TOHEAD AND NECK-CANCER

      Journal of Clinical Pathology
    37. BATALLA A; CUBERO GI; REGUERO JR; COTO E
      PLATELET PIA POLYMORPHISM, MYOCARDIAL-INFARCTION, AND EXTENT OF CORONARY-ARTERY DISEASE

      Circulation
    38. ALVAREZ R; REGUERO JR; BATALLA A; IGLESIASCUBERO G; CORTINA A; ALVAREZ V; COTO E
      ANGIOTENSIN-CONVERTING ENZYME AND ANGIOTENSIN-II RECEPTOR-1 POLYMORPHISMS - ASSOCIATION WITH EARLY CORONARY-DISEASE

      Cardiovascular Research
    39. Reguero, JR; Cubero, GI; Batalla, A; Alvarez, V; Hevia, S; Cortina, A; Coto, E
      Apolipoprotein A1 gene polymorphisms and risk of early coronary disease

      CARDIOLOGY
    40. ARIZA M; ALVAREZ V; MARIN R; AGUADO S; LOPEZLARREA C; ALVAREZ J; MENENDEZ MJ; COTO E
      A FAMILY WITH A MILDER FORM OF ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE NOT LINKED TO THE PKD1 (16P) OR PKD2 (4Q) GENES

      Journal of Medical Genetics
    41. GONZALEZ MV; PELLO MF; LOPEZLARREA C; SUAREZ C; MENENDEZ MJ; COTO E
      DELETION AND METHYLATION OF THE TUMOR-SUPPRESSOR GENE P16 CDKN2 IN PRIMARY HEAD AND NECK SQUAMOUS-CELL CARCINOMA/

      Journal of Clinical Pathology
    42. GONZALEZ MV; ARTIMEZ ML; RODRIGO L; LOPEZLARREA C; MENENDEZ MJ; ALVAREZ V; PEREZ R; FRESNO MF; PEREZ MJ; SAMPEDRO A; COTO E
      MUTATION ANALYSIS OF THE P53, APC, AND P16 GENES IN THE BARRETTS-ESOPHAGUS, DYSPLASIA, AND ADENOCARCINOMA

      Journal of Clinical Pathology
    43. BATALLA A; REGUERO JJR; CUBERO GI; MOLINA BD; BRAGA S; MENENDEZ MJ; COTO E; CORTINA A
      POLYMORPHISMS OF THE PLATELET RECEPTOR IIIA IN EARLY CORONARY-DISEASE

      Atherosclerosis
    44. BATALLA A; REGUERO JJR; CUBERO GI; MOLINA BD; BRAGA S; HEVIA S; MENENDEZ MJ; COTO E; CORTINA A
      POLYMORPHISMS AT THE 5'-END OF THE APOLIPOPROTEIN AI GENE AND EARLY CORONARY-DISEASE

      Atherosclerosis
    45. BATALLA A; REGUERO JJR; CUBERO GI; MOLINA BD; BRAGA S; HEVIA S; MENENDEZ MJ; COTO E; CORTINA A
      POLYMORPHISMS OF THE PLATELET RECEPTOR IIIA AND LIPID-LEVELS IN EARLYCORONARY-DISEASE

      Atherosclerosis
    46. BATALLA A; REGUERO JJR; CUBERO GI; MOLINA BD; BRAGA S; HEVIA S; MENENDEZ MJ; COTO E; CORTINA A
      POLYMORPHISMS AT THE 5'-END OF THE APOLIPOPROTEIN AL GENE AND LIPID-LEVELS IN EARLY CORONARY-DISEASE

      Atherosclerosis
    47. GARCIAGALA JM; ALVAREZ V; PINTO CR; SOTO I; URGELLES MF; MENENDEZ MJ; CARRACEDO C; LOPEZLARREA C; COTO E
      FACTOR-V-LEIDEN (R506Q) AND RISK OF VENOUS THROMBOEMBOLISM - A CASE-CONTROL STUDY BASED ON THE SPANISH POPULATION

      Clinical genetics
    48. VELDHUISEN B; SARIS JJ; DEHAIJ S; HAYASHI T; REYNOLDS DM; MOCHIZUKI T; ELLES R; FOSSDAL R; BOGDANOVA N; VANDIJK MA; COTO E; RAVINE D; NORBY S; VERELLENDUMOULIN C; BREUNING MH; SOMLO S; PETERS DJM
      A SPECTRUM OF MUTATIONS IN THE 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD2)

      American journal of human genetics
    49. GONZALEZROCES S; ALVAREZ MV; GONZALEZ S; DIEYE A; MAKNI H; WOODFIELD DG; HOUSAN L; KONENKOV V; ABBADI MC; GRUNNET N; COTO E; LOPEZLARREA C
      HLA-B27 POLYMORPHISM AND WORLDWIDE SUSCEPTIBILITY TO ANKYLOSING-SPONDYLITIS

      Tissue antigens
    50. PETERS DJM; VELDHUISEN B; SARIS JJ; HAYASHI T; MOCHIZUKI T; REYNOLDS DM; COTO E; FOSSDAL R; ELLES R; SOMLO S; BREUNING MH
      THE SPECTRUM OF MUTATIONS IN THE POLYCYSTIC KIDNEY-DISEASE-2 (PKD2) GENE

      Journal of the American Society of Nephrology
    51. HAYASHI T; MOCHIZUKI T; WATNICK TJ; REYNOLDS DM; WU GQ; CAI Y; COTO E; GERMINO G; LENS X; SOMLO S
      GENOMIC ORGANIZATION AND MUTATIONS IN THE 2ND GENE FOR POLYCYSTIC KIDNEY-DISEASE (PKD2)

      Journal of the American Society of Nephrology
    52. GONZALEZ S; SETIEN F; COTO E; LOPEZLARREA C
      GENETIC-STRUCTURE AND ORGANIZATION OF THE MEMBRANE ATTACK COMPLEMENT COMPONENTS

      European journal of immunogenetics
    53. ALVAREZ V; COTO E; SETIEN F; GONZALEZROCES S; LOPEZLARREA C
      MOLECULAR EVOLUTION OF THE N-FORMYL PEPTIDE AND C5A RECEPTORS IN NONHUMAN-PRIMATES

      Immunogenetics
    54. ALVAREZ V; COTO E; SETIEN F; GONZALEZ S; GONZALEZROCES S; LOPEZLARREA C
      CHARACTERIZATION OF INLERLEUKIN-8 RECEPTORS IN NONHUMAN-PRIMATES

      Immunogenetics
    55. GONZALEZ MV; PELLO MF; LOPEZLARREA C; SUAREZ C; MENENDEZ MJ; COTO E
      LOSS OF HETEROZYGOSITY AND MUTATION ANALYSIS OF THE P16 (9P21) AND P53 (17P13) GENES IN SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK

      Clinical cancer research
    56. COTO E; AGUADO S; MENENDEZ MJ; ALVAREZ J; DECASTRO SS; ARIAS M; LOPEZLARREA C
      MOLECULAR-BIOLOGY IN AUTOSOMAL-DOMINANT A DULT POLYCYSTIC KIDNEY

      Nefrologia
    57. COTO E
      THE DIAGNOSIS OF ADULT RENAL POLYCYTIC DI SEASE AT MOLECULAR-LEVEL

      Nefrologia
    58. LOPEZLARREA C; GONZALEZROCES S; PENA M; DOMINGUEZ O; COTO E; ALVAREZ V; MORENO M; HERNANDEZ O; BURGOSVARGAS R; GORODEZKY C
      CHARACTERIZATION OF B27 HAPLOTYPES BY OLIGOTYPING AND GENOMIC SEQUENCING IN THE MEXICAN MESTIZO POPULATION WITH ANKYLOSING-SPONDYLITIS - JUVENILE AND ADULT-ONSET

      Human immunology
    59. COTO E; TORAL JF; MENENDEZ MJ; HERNANDO I; PLASENCIA A; BENAVIDES A; LOPEZLARREA C
      PCR-BASED STUDY OF THE PRESENCE OF Y-CHROMOSOME SEQUENCES IN PATIENTSWITH ULLRICH-TURNER SYNDROME

      American journal of medical genetics
    60. ALVAREZ V; COTO E; SETIEN F; SPATH PJ; LOPEZLARREA C
      GENETIC DETECTION OF THE SILENT ALLELE (ASTERISK-Q0) IN HEREDITARY DEFICIENCIES OF THE HUMAN-COMPLEMENT C6, C7, AND C9 COMPONENTS

      American journal of medical genetics
    61. COTO E; DECASTRO SS; AGUADO S; ALVAREZ J; ARIAS M; MENENDEZ MJ; LOPEZLARREA C
      DNA MICROSATELLITE ANALYSIS OF FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE TYPE-1 AND TYPE-2 - EVALUATION OF CLINICAL HETEROGENEITY BETWEEN BOTH FORMS OF THE DISEASE

      Journal of Medical Genetics
    62. LOPEZLARREA C; SUJIRACHATO K; MEHRA NK; CHIEWSILP P; ISARANGKURA D; KANGA U; DOMINGUEZ O; COTO E; PENA M; SETIEN F; GONZALEZROCES S
      HLA-B27 SUBTYPES IN ASIAN PATIENTS WITH ANKYLOSING-SPONDYLITIS

      Tissue antigens
    63. BARANDA FS; COTO E; DIAZ JM; MARTINEZNAVES E; MARTINEZ VA; LOPEZLARREA C
      HLA CLASS-II AND SUSCEPTIBILITY AND RESISTANCE TO INSULIN-DEPENDENT DIABETES-MELLITUS IN A POPULATION FROM THE NORTHWEST OF SPAIN

      European journal of immunogenetics
    64. COTO E; AGUADO S; MENENDEZ MJ; ALVAREZ J; DECASTRO SS; ARIAS M; LOPEZLARREA C
      MOLECULAR-BIOLOGY IN AUTOSOMAL-DOMINANT A DULT POLYCYSTIC KIDNEY-DISEASE

      Nefrologia
    65. GONZALEZROCES S; BRAUTBAR C; PENA M; DOMINGUEZ O; COTO E; ALVAREZ V; SEGAL R; LOPEZLARREA C
      MOLECULAR ANALYSIS OF HLA-B27 HAPLOTYPES IN CAUCASOIDS - FREQUENCIES OF B27-CW IN JEWISH AND SPANISH POPULATIONS

      Human immunology
    66. ALVAREZ V; COTO E; SETIEN F; LOPEZLARREA C
      A PHYSICAL MAP OF 2 CLUSTERS CONTAINING THE GENES FOR 6 PROINFLAMMATORY RECEPTORS

      Immunogenetics
    67. HERNANDEZ F; RODRIGUEZ E; GAMBOA MD; COTO E; DELOSACUNA M
      ULTRASTRUCTURAL VIEW OF THE BACTERIUM MOBILUCUS-MULIERIS - AN APPROACH TO UNDERSTAND SOME PROBLEMS FOR THEIR ISOLATION

      Revista de biologia tropical
    68. COTO E; BOUSONO C; MENENDEZ MJ; CUE R; TORAL JF; BENAVIDES A; HERNANDO I
      CYSTIC-FIBROSIS IN ASTURIAS (SPAIN) - HIG H-FREQUENCY OF THE DELTA-F508 MUTATION

      Medicina Clinica
    69. FUENTES JJ; VOLPINI V; FERNANDEZTORAL F; COTO E; ESTIVILL X
      IDENTIFICATION OF 2 NEW MISSENSE MUTATIONS (K58N AND R121Q) IN THE NORRIE DISEASE (ND) GENE IN 2 SPANISH FAMILIES

      Human molecular genetics
    70. SETIEN F; ALVAREZ V; COTO E; DISCIPIO RG; LOPEZLARREA C
      A PHYSICAL MAP OF THE HUMAN-COMPLEMENT COMPONENT C6, C7, AND C9 GENES

      Immunogenetics


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Documento generato il 23/01/21 alle ore 10:17:32