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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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31157679
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Bravo-Perez C, Vicente V, Corral J. Management of antithrombin deficiency: an update for clinicians. Expert Rev Hematol. 2019 Jun;12(6):397-405. doi: 10.1080/17474086.2019.1611424. Epub 2019 May 22. PubMed PMID: 31116611.
AÑO: 2019; IF: 2.573
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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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De la Morena-Barrio B, Borras N, Rodriguez-Alen A, de la Morena-Barrio ME, Garcia-Hernandez JL, Padilla J, Bravo-Perez C, Minano A, Rollon N, Corral J, Vidal F, Vicente V. Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods. Br J Haematol. 2019 Aug;186(4):e82-e86. doi: 10.1111/bjh.15913. Epub 2019 Apr 2. No abstract available. PubMed PMID: 30941754.
AÑO: 2019; IF: 5.518
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