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Zaragoza-Huesca D, Nieto-Olivares A, Garcia-Molina F, Ricote G, Montenegro S, Sanchez-Canovas M, Garrido-Rodriguez P, Penas-Martinez J, Vicente V, Martinez F, Lozano ML, Carmona-Bayonas A, Martinez-Martinez I. Implication of Hepsin from Primary Tumor in the Prognosis of Colorectal Cancer Patients. Cancers (Basel). 2022 Jun 24;14(13):3106. doi: 10.3390/cancers14133106. PubMed PMID: 35804878; PubMed Central PMCID: PMC9264764.
AÑO: 2022; IF: 6.575
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35804878
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de la Morena-Barrio ME, Corral J, Lopez-Garcia C, Jimenez-Diaz VA, Minano A, Juan-Salvadores P, Esteve-Pastor MA, Baz-Alonso JA, Rubio AM, Sarabia-Tirado F, Garcia-Navarro M, Garcia-Lara J, Marin F, Vicente V, Pinar E, Canovas SJ, de la Morena G. Contact pathway in surgical and transcatheter aortic valve replacement. Front Cardiovasc Med. 2022 Jul 22;9:887664. doi: 10.3389/fcvm.2022.887664. eCollection 2022. PubMed PMID: 35935621; PubMed Central PMCID: PMC9354960.
AÑO: 2022; IF: 3.6
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Palma-Barqueros V, Bury L, Kunishima S, Lozano ML, Rodriguez-Alen A, Revilla N, Bohdan N, Padilla J, Fernandez-Perez MP, de la Morena-Barrio ME, Marin-Quilez A, Benito R, Lopez-Fernandez MF, Marcellini S, Zamora-Canovas A, Vicente V, Martinez C, Gresele P, Bastida JM, Rivera J. Expanding the genetic spectrum of TUBB1-related thrombocytopenia. Blood Adv. 2021 Dec 28;5(24):5453-5467. doi: 10.1182/bloodadvances.2020004057. Erratum In: Blood Adv. 2023 Mar 28;7(6):877. PubMed PMID: 34516618; PubMed Central PMCID: PMC8714720.
AÑO: 2021; IF: 7.637
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Palma-Barqueros V, Revilla N, Sanchez A, Zamora Canovas A, Rodriguez-Alen A, Marin-Quilez A, Gonzalez-Porras JR, Vicente V, Lozano ML, Bastida JM, Rivera J. Inherited Platelet Disorders: An Updated Overview. Int J Mol Sci. 2021 Apr 26;22(9):4521. doi: 10.3390/ijms22094521. PubMed PMID: 33926054; PubMed Central PMCID: PMC8123627.
AÑO: 2021; IF: 6.208
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Orlando C, de la Morena-Barrio B, Pareyn I, Vanhoorelbeke K, Martinez-Martinez I, Vicente V, Corral J, Jochmans K, de la Morena-Barrio ME. Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency. Thromb Haemost. 2021 Feb;121(2):182-191. doi: 10.1055/s-0040-1716531. Epub 2020 Sep 13. PubMed PMID: 32920809.
AÑO: 2021; IF: 6.681
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