Coto E - Search Results

1

Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia.

Aparicio A, Villazón F, Suárez-Gutiérrez L, Gómez J, Martínez-Faedo C, Méndez-Torre E, Avanzas P, Álvarez-Velasco R, Cuesta-Llavona E, García-Lago C, Neuhalfen D, Coto E, Lorca R. Aparicio A, et al. Among authors: coto e. J Clin Med. 2023 Jan 29;12(3):1030. doi: 10.3390/jcm12031030. J Clin Med. 2023. PMID: 36769678 Free PMC article.

2

Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.

Valdes N, Alvarez V, Diaz-Cadorniga F, Aller J, Villazon F, Garcia I, Herrero A, Coto E. Valdes N, et al. Among authors: coto e. Anticancer Res. 1998 Jul-Aug;18(4A):2685-9. Anticancer Res. 1998. PMID: 9703929

3

Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population.

Román-García P, Coto E, Reguero JR, Cannata-Andía JB, Lozano I, Avanzas P, Morís C, Rodríguez I. Román-García P, et al. Among authors: coto e. Coron Artery Dis. 2009 Sep;20(6):383-6. doi: 10.1097/MCA.0b013e32832fa9cf. Coron Artery Dis. 2009. PMID: 19620856

4

Lack of association between endothelin-1 gene variants and myocardial infarction.

Palacín M, Rodriguez-Pascual F, Reguero JR, Rodríguez I, Avanzas P, Lozano I, Morís C, Alvarez V, Cannata-Andía JB, Lamas S, García-Castro M, Coto E. Palacín M, et al. Among authors: coto e. J Atheroscler Thromb. 2009 Aug;16(4):388-95. doi: 10.5551/jat.no1149. Epub 2009 Aug 11. J Atheroscler Thromb. 2009. PMID: 19672034 Free article.

5

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.

Palacín M, Alvarez V, Martín M, Díaz M, Corao AI, Alonso B, Díaz-Molina B, Lozano I, Avanzas P, Morís C, Reguero JR, Rodríguez I, López-Larrea C, Cannata-Andía J, Batalla A, Ruiz-Ortega M, Martínez-Camblor P, Coto E. Palacín M, et al. Among authors: coto e. Mitochondrion. 2011 Jan;11(1):176-81. doi: 10.1016/j.mito.2010.09.004. Epub 2010 Sep 21. Mitochondrion. 2011. PMID: 20863902

6

Common European mitochondrial haplogroups in the risk for psoriasis and psoriatic arthritis.

Coto-Segura P, Santos-Juanes J, Gómez J, Alvarez V, Díaz M, Alonso B, Corao AI, Coto E. Coto-Segura P, et al. Among authors: coto e. Genet Test Mol Biomarkers. 2012 Jun;16(6):621-3. doi: 10.1089/gtmb.2011.0266. Epub 2011 Dec 22. Genet Test Mol Biomarkers. 2012. PMID: 22191676

7

Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes.

Eiris N, Santos-Juanes J, Coto-Segura P, Gómez J, Alvarez V, Morales B, Queiro R, Díaz M, Corao AI, López-Corte K, Coto E. Eiris N, et al. Among authors: coto segura p, coto e. Cytokine. 2012 Oct;60(1):27-9. doi: 10.1016/j.cyto.2012.05.030. Epub 2012 Jun 26. Cytokine. 2012. PMID: 22739501

8

Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.

Tavira B, Coto E, Gómez J, Tranche S, Miguélez K, Ortega F, Díez B, Sánchez E, Marín R, Arenas J, Alvarez V. Tavira B, et al. Among authors: coto e. Gene. 2013 May 10;520(1):73-6. doi: 10.1016/j.gene.2013.02.024. Epub 2013 Mar 5. Gene. 2013. PMID: 23470845

9

A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort.

Tavira B, Gómez J, Ortega F, Tranche S, Díaz-Corte C, Alvarez F, Ortiz A, Santos F, Sánchez-Niño MD, Coto E. Tavira B, et al. Among authors: coto e. Gene. 2013 Sep 25;527(2):670-2. doi: 10.1016/j.gene.2013.06.055. Epub 2013 Jul 9. Gene. 2013. PMID: 23850580

10

A Common APOE Polymorphism Is an Independent Risk Factor for Reduced Glomerular Filtration Rate in the Spanish RENASTUR Cohort.

Coto E, Gómez J, Tavira B, Tranche S, Ortega F, Rodríguez MI, Sánchez E, Marín R, Corao AI, Arenas J, Alvarez V. Coto E, et al. Cardiorenal Med. 2013 Jul;3(2):113-119. doi: 10.1159/000351158. Epub 2013 May 16. Cardiorenal Med. 2013. PMID: 23922551 Free PMC article.

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