|
García-López R, de la Morena-Barrio ME, Alsina L, Pérez-Dueñas B, Jaeken J, Serrano M, Casado M, Hernández-Caselles T. Natural Killer Cell Receptors and Cytotoxic Activity in Phosphomannomutase 2 Deficiency (PMM2-CDG). PLoS One. 2016 Jul 14;11(7):e0158863. doi: 10.1371/journal.pone.0158863. eCollection 2016. Erratum in: PLoS One. 2016 Oct 27;11(10 ):e0165901. PubMed PMID: 27415628; PubMed Central PMCID: PMC4944953.
AÑO: 2016; IF: 2.806
|
27415628
|
Motlló C, Ribera JM, Morgades M, Granada I, Montesinos P, Mercadal S, González-Campos J, Moreno MJ, Barba P, Cervera M, Barrios M, Novo A, Bernal T, Hernández-Rivas JM, Abella E, Amigo ML, Tormo M, Martino R, Lavilla E, Bergua J, Serrano A, García-Belmonte D, Guàrdia R, Grau J, Feliu E; PETHEMA Group, Spanish Society of Hematology. Frequency and prognostic significance of additional cytogenetic abnormalities to the Philadelphia chromosome in young and older adults with acute lymphoblastic leukemia. Leuk Lymphoma. 2018 Jan;59(1):146-154. doi: 10.1080/10428194.2017.1326596. Epub 2017 May 30. PubMed PMID: 28554259.
AÑO: 2018; IF: 2.674
|
|
Zeng W, Hu B, Tang L, You YY, Toderici M, de la Morena-Barrio ME, Corral J, Hu Y. Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency. Oncotarget. 2017 Sep 28;8(48):84417-84425. doi: 10.18632/oncotarget.21365. eCollection 2017 Oct 13. Erratum in: Oncotarget. 2018 Feb 16;9(13):11428. PubMed PMID: 29137435; PubMed Central PMCID: PMC5663607.
AÑO: 2017; IF: 5.168
|
|
Esteban J, de la Morena-Barrio ME, Salloum-Asfar S, Padilla J, Miñano A, Roldán V, Soria JM, Vidal F, Corral J, Vicente V. High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study. Haemophilia. 2017 Nov;23(6):e488-e496. doi: 10.1111/hae.13356. Epub 2017 Sep 27. PubMed PMID: 28960694.
AÑO: 2017; IF: 2.768
|
|
de la Morena-Barrio ME, Ballesta-Martínez MJ, López-Gálvez R, Antón AI, López-González V, Martínez-Ribot L, Padilla J, Miñano A, García-Algar O, Del Campo M, Corral J, Guillén-Navarro E, Vicente V. Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation. Pediatr Res. 2018 Jan;83(1-1):119-127. doi: 10.1038/pr.2017.201. Epub 2017 Sep 20. PubMed PMID: 28820871.
AÑO: 2018; IF: 2.88
|