|
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
|
31043424
|
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
|
|
Bravo-Perez C, Rodenas T, Esteban J, de la Morena-Barrio ME, Salloum-Asfar S, de la Morena-Barrio B, Minano A, Vicente V, Corral J. Gynaecological and obstetrical bleeding in Caucasian women with congenital factor XI deficiency: Results from a twenty-year, retrospective, observational study. Med Clin (Barc). 2019 Nov 29;153(10):373-379. doi: 10.1016/j.medcli.2019.01.029. Epub 2019 Mar 26. English, Spanish. PubMed PMID: 30926156.
AÑO: 2019; IF: 1.635
|
|
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
|
|
Lopez-Galvez R, de la Morena-Barrio ME, Lopez-Lera A, Pathak M, Minano A, Serrano M, Borgel D, Roldan V, Vicente V, Emsley J, Corral J. Factor XII in PMM2-CDG patients: role of N-glycosylation in the secretion and function of the first element of the contact pathway. Orphanet J Rare Dis. 2020 Oct 9;15(1):280. doi: 10.1186/s13023-020-01564-9. PubMed PMID: 33036649; PubMed Central PMCID: PMC7547467.
AÑO: 2020; IF: 4.123
|