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de la Morena-Barrio ME, Wypasek E, Owczarek D, Minano A, Vicente V, Corral J, Undas A. MPI-CDG with transient hypoglycosylation and antithrombin deficiency. Haematologica. 2019 Feb;104(2):e79-e82. doi: 10.3324/haematol.2018.211326. Epub 2018 Dec 13. No abstract available. PubMed PMID: 30545931; PubMed Central PMCID: PMC6355499.
AÑO: 2019; IF: 7.116
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30545931
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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
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Navarro-Fernández J, Eugenia de la Morena-Barrio M, Martínez-Alonso E, Dybedal I, Toderici M, Bohdan N, Miñano A, Heimdal K, Abildgaard U, Martínez-Menárguez JÁ, Corral J, Vicente V. Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family. Oncotarget. 2018 Sep 4;9(69):33202-33214. doi: 10.18632/oncotarget.26059. eCollection 2018 Sep 4. PubMed PMID: 30237862; PubMed Central PMCID: PMC6145704.
AÑO: 2018
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de la Morena-Barrio B, de la Morena-Barrio ME, Padilla J, Teruel-Montoya R, Asenjo S, Wypasek E, Undas A, Miñano A, Vicente V, Corral J. Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6. Thromb Haemost. 2018 May;118(5):939-941. doi: 10.1055/s-0038-1637721. Epub 2018 Mar 21. PubMed PMID: 29564838.
AÑO: 2018; IF: 4.733
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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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