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Salloum-Asfar S, de la Morena-Barrio ME, Esteban J, Miñano A, Aroca C, Vicente V, Roldán V, Corral J. Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency. Thromb Res. 2018 Mar;163:64-70. doi: 10.1016/j.thromres.2017.12.023. Epub 2018 Jan 3. PubMed PMID: 29367083.
AÑO: 2018; IF: 3.266
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29367083
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Pascreau T, de la Morena-Barrio ME, Lasne D, Serrano M, Bianchini E, Kossorotoff M, Boddaert N, Bruneel A, Seta N, Vicente V, de Lonlay P, Corral J, Borgel D. Elevated thrombin generation in patients with congenital disorder of glycosylation and combined coagulation factor deficiencies. J Thromb Haemost. 2019 Nov;17(11):1798-1807. doi: 10.1111/jth.14559. Epub 2019 Jul 28. PubMed PMID: 31271700.
AÑO: 2019; IF: 4.385
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Wojcik M, de la Morena-Barrio ME, Michalik J, Wypasek E, Kopytek M, Corral J, Undas A. A series of 10 Polish patients with thromboembolic events and antithrombin deficiency: two new c.1154-1 G>C and c.1219-534 A>G SERPINC1 gene splicing mutations. Blood Coagul Fibrinolysis. 2019 Jul;30(5):193-198. doi: 10.1097/MBC.0000000000000816. PubMed PMID: 31157679.
AÑO: 2019; IF: 1.203
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de la Morena-Barrio ME, Salloum-Asfar S, Esteban J, de la Morena-Barrio B, Altisent C, Martin-Fernandez L, Gueguen P, Padilla J, Minano A, Parra R, Vicente V, Vidal F, Bauduer F, Carbonell P, Corral J. Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries. Blood. 2019 Jun 13;133(24):2618-2622. doi: 10.1182/blood.2019000055. Epub 2019 May 1. No abstract available. PubMed PMID: 31043424.
AÑO: 2019; IF: 25.476
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de la Morena-Barrio B, Orlando C, de la Morena-Barrio ME, Vicente V, Jochmans K, Corral J. Incidence and features of thrombosis in children with inherited antithrombin deficiency. Haematologica. 2019 Dec;104(12):2512-2518. doi: 10.3324/haematol.2018.210666. Epub 2019 Apr 11. PubMed PMID: 30975910; PubMed Central PMCID: PMC6959168.
AÑO: 2019; IF: 7.116
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