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de la Morena-Barrio ME, Antón AI, Martínez-Martínez I, Padilla J, Miñano A, Navarro-Fernández J, Águila S, López MF, Fontcuberta J, Vicente V, Corral J. Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency. Thromb Haemost. 2012 Mar;107(3):430-7. doi: 10.1160/TH11-10-0701. Epub 2012 Jan 11. PubMed PMID: 22234719.
AÑO: 2012; IF: 5.249
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22234719
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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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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, Navarro-Fernández J, Østergaard A, Gutiérrez-Gallego R, Padilla J, Bohdan N, Miñano A, Pascual C, Martínez C, de la Morena-Barrio ME, Aguila S, Pedersen S, Kristensen SR, Vicente V, Corral J. Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism. Blood. 2012 Jul 26;120(4):900-4. doi: 10.1182/blood-2012-01-406207. Epub 2012 Apr 12. PubMed PMID: 22498748.
AÑO: 2012; IF: 22.113
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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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