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Wypasek E, Corral J, Alhenc-Gelas M, Sydor W, Iwaniec T, Celińska-Lowenhoff M, Potaczek DP, Blecharczyk A, Zawilska K, Musiał J, Undas A. Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients. Pol Arch Intern Med. 2017 Aug 9;127(7-8):512-523. doi: 10.20452/pamw.4045. Epub 2017 Jun 13. PubMed PMID: 28607330.
AÑO: 2017; IF: 2.658
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28607330
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de la Morena-Barrio ME, López-Gálvez R, Martínez-Martínez I, Asenjo S, Sevivas TS, López MF, Wypasek E, Entrena L, Vicente V, Corral J. Defects of splicing in antithrombin deficiency. Res Pract Thromb Haemost. 2017 Jul 14;1(2):216-222. doi: 10.1002/rth2.12025. eCollection 2017 Oct. PubMed PMID: 30046692; PubMed Central PMCID: PMC6058262.
AÑO: 2017
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Revilla N, de la Morena-Barrio ME, Miñano A, López-Gálvez R, Toderici M, Padilla J, García-Avello Á, Lozano ML, Lefeber DJ, Corral J, Vicente V. Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy. Sci Rep. 2017 Mar 17;7:44556. doi: 10.1038/srep44556. PubMed PMID: 28303970; PubMed Central PMCID: PMC5355981.
AÑO: 2017; IF: 4.122
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de la Morena-Barrio M, Sandoval E, Llamas P, Wypasek E, Toderici M, Navarro-Fernández J, Rodríguez-Alen A, Revilla N, López-Gálvez R, Miñano A, Padilla J, de la Morena-Barrio B, Cuesta J, Corral J, Vicente V. High levels of latent antithrombin in plasma from patients with antithrombin deficiency. Thromb Haemost. 2017 May 3;117(5):880-888. doi: 10.1160/TH16-11-0866. Epub 2017 Feb 23. PubMed PMID: 28229161.
AÑO: 2017; IF: 4.952
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Vossen CY, van Hylckama Vlieg A, Teruel-Montoya R, Salloum-Asfar S, de Haan H, Corral J, Reitsma P, Koeleman BPC, Martínez C. Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs. Br J Haematol. 2017 Jun;177(5):782-790. doi: 10.1111/bjh.14629. Epub 2017 Apr 26. PubMed PMID: 28444748.
AÑO: 2017; IF: 5.128
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