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Bravo-Perez C, de la Morena-Barrio ME, Vicente V, Corral J. Antithrombin deficiency as a still underdiagnosed thrombophilia: a primer for internists. Pol Arch Intern Med. 2020 Oct 29;130(10):868-877. doi: 10.20452/pamw.15371. Epub 2020 May 19. PubMed PMID: 32426958.
AÑO: 2020; IF: 3.277
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32426958
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Corvillo F, de la Morena-Barrio ME, Marcos-Bravo C, Lopez-Trascasa M, Vicente V, Emsley J, Caballero T, Corral J, Lopez-Lera A. The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant. Front Genet. 2020 Sep 10;11:1033. doi: 10.3389/fgene.2020.01033. eCollection 2020. PubMed PMID: 33133137; PubMed Central PMCID: PMC7549737.
AÑO: 2020; IF: 4.599
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Bravo-Perez C, de la Morena-Barrio ME, Palomo A, Entrena L, de la Morena-Barrio B, Padilla J, Minano A, Navarro E, Cifuentes R, Corral J, Vicente V. Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo. Br J Haematol. 2020 Oct;191(1):e32-e35. doi: 10.1111/bjh.16963. Epub 2020 Jul 19. No abstract available. PubMed PMID: 32686144.
AÑO: 2020; IF: 6.998
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de la Morena-Barrio ME, Sabater M, de la Morena-Barrio B, Ruhaak RL, Minano A, Padilla J, Toderici M, Roldan V, Gimeno JR, Vicente V, Corral J. ALG12-CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant. Mol Genet Genomic Med. 2020 Aug;8(8):e1304. doi: 10.1002/mgg3.1304. Epub 2020 Jun 12. PubMed PMID: 32530140; PubMed Central PMCID: PMC7434597.
AÑO: 2020; IF: 2.183
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Baiges A, de la Morena-Barrio ME, Turon F, Minano A, Alberto Ferrusquia J, Magaz M, Reverter JC, Vicente V, Hernandez-Gea V, Corral J, Garcia-Pagan JC. Congenital antithrombin deficiency in patients with splanchnic vein thrombosis. Liver Int. 2020 May;40(5):1168-1177. doi: 10.1111/liv.14342. Epub 2020 Jan 16. PubMed PMID: 31885188.
AÑO: 2020; IF: 5.828
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