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de la Morena-Barrio ME, Sevivas TS, Martinez-Martinez I, Miñano A, Vicente V, Jaeken J, Corral J. Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia. J Thromb Haemost. 2012 Dec;10(12):2625-7. doi: 10.1111/jth.12031. PubMed PMID: 23082948.
AÑO: 2012; IF: 6.081
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23082948
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Martínez-Martínez I, Navarro-Fernández J, Aguila S, Miñano A, Bohdan N, De La Morena-Barrio ME, Ordóñez A, Martínez C, Vicente V, Corral J. The infective polymerization of conformationally unstable antithrombin mutants may play a role in the clinical severity of antithrombin deficiency. Mol Med. 2012 Jul 18;18:762-70. doi: 10.2119/molmed.2012.00017. PubMed PMID: 22481271; PubMed Central PMCID: PMC3409284.
AÑO: 2012; IF: 6.354
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Martínez-Martínez I, Ordóñez A, Pedersen S, de la Morena-Barrio ME, Navarro-Fernández J, Kristensen SR, Miñano A, Padilla J, Vicente V, Corral J. Heparin affinity of factor VIIa: implications on the physiological inhibition by antithrombin and clearance of recombinant factor VIIa. Thromb Res. 2011 Feb;127(2):154-60. doi: 10.1016/j.thromres.2010.11.008. Epub 2010 Dec 3. PubMed PMID: 21126754.
AÑO: 2011; IF: 3.944
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Navarro-Núñez L, Teruel R, Antón AI, Nurden P, Martínez-Martínez I, Lozano ML, Rivera J, Corral J, Mezzano D, Vicente V, Martinez C. Rare homozygous status of P43 ?1-tubulin polymorphism causes alterations in platelet ultrastructure. Thromb Haemost. 2011 May;105(5):855-63. doi: 10.1160/TH10-08-0536. Epub 2011 Mar 8. PubMed PMID: 21384078.
AÑO: 2011; IF: 5.044
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Teruel R, Corral J, Pérez-Andreu V, Martínez-Martínez I, Vicente V, Martínez C. Potential role of miRNAs in developmental haemostasis. PLoS One. 2011 Mar 9;6(3):e17648. doi: 10.1371/journal.pone.0017648. PubMed PMID: 21408009; PubMed Central PMCID: PMC3052364.
AÑO: 2011; IF: 4.092
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