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Sánchez-Guiu I, Antón AI, García-Barberá N, Navarro-Fernández J, Martínez C, Fuster JL, Couselo JM, Ortuño FJ, Vicente V, Rivera J, Lozano ML. Chediak-Higashi syndrome: description of two novel homozygous missense mutations causing divergent clinical phenotype. Eur J Haematol. 2014 Jan;92(1):49-58. doi: 10.1111/ejh.12203. PubMed PMID: 24112114.
AÑO: 2014; IF: 2.066
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24112114
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de la Morena-Barrio ME, Buil A, Antón AI, Martínez-Martínez I, Miñano A, Gutiérrez-Gallego R, Navarro-Fernández J, Aguila S, Souto JC, Vicente V, Soria JM, Corral J. Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins? PLoS One. 2013 May 21;8(5):e64998. doi: 10.1371/journal.pone.0064998. PubMed PMID: 23705025; PubMed Central PMCID: PMC3660365.
AÑO: 2013; IF: 3.24
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Anton AI, Cerezo-Manchado JJ, Padilla J, Perez-Andreu V, Corral J, Vicente V, Roldan V, Gonzalez-Conejero R. Novel associations of VKORC1 variants with higher acenocoumarol requirements. PLoS One. 2013 May 17;8(5):e64469. doi: 10.1371/journal.pone.0064469. PubMed PMID: 23691226; PubMed Central PMCID: PMC3656883.
AÑO: 2013; IF: 3.534
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Águila S, Martínez-Martínez I, Collado M, Llamas P, Antón AI, Martínez-Redondo C, Padilla J, Miñano A, de la Morena-Barrio ME, Garcia-Avello Á, Vicente V, Corral J. Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency. Thromb Haemost. 2013 Mar;109(3):556-8. doi: 10.1160/TH12-09-0707. PubMed PMID: 23329010.
AÑO: 2013; IF: 5.76
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Cerezo-Manchado JJ, Rosafalco M, Antón AI, Pérez-Andreu V, Garcia-Barberá N, Martinez AB, Corral J, Vicente V, González-Conejero R, Roldán V. Creating a genotype-based dosing algorithm for acenocoumarol steady dose. Thromb Haemost. 2013 Jan;109(1):146-53. doi: 10.1160/TH12-08-0631. PubMed PMID: 23196355.
AÑO: 2013; IF: 5.76
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