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Diaz-Ajenjo L, Marin-Quilez A, Lama-Villanueva A, Garcia-Jaen P, Rey-Bua B, Hernandez-Rivas JM, Morgan NV, Gonzalez-Porras JR, Benito R, Rivera J, Bastida JM. A novel homozygous splice-site variant in VPS33B identified as a cause of bleeding. J Thromb Haemost. 2026 Jan;24(1):146-154. doi: 10.1016/j.jtha.2025.09.036. Epub 2025 Oct 23. PubMed PMID: 41138802.
AÑO: 2026; IF: 5.0
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41138802
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Di Buduo CA, Abbonante V, Malara A, Balduini A, Waller AK, Watson SP, Martin EM, Bridge L, Gibbins J, Hers I, Masson C, Eckly A, Poulter NS, Martinez-Garcia B, Aguila S, Gresele P, Momi S, Amstrong P, Rondina M, Troitino S, Garcia A, Bastida JM, Quilez AM, Fuentes AS, Rivera J, Torres-Ruiz R, Ojeda-Walczuk P, Morgan NV, Morena B, Ramaekers K, Tran M, De Wispelaere K, Freson K, Bergmeier W, Greinacher A, He F, Oh S, Di Paola J, Semple JW, Lozano ML, Llamas P, Ward C. Illustrated capsules from the Advanced Course in Platelet Research. Res Pract Thromb Haemost. 2025 Feb 27;9(2):102715. doi: 10.1016/j.rpth.2025.102715. eCollection 2025 Feb. PubMed PMID: 40177221; PubMed Central PMCID: PMC11964540.
AÑO: 2025; IF: 3.4
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Marin-Quilez A, Sanchez-Fuentes A, Zamora-Canovas A, Gomez-Gonzalez PL, Diaz-Ajenjo L, Benito R, Rodriguez-Alen A, Sevivas T, Murciano T, Murillo L, Butta NV, Revilla N, Campos R, Escribano P, Esteve J, Fernandez-Mosteirin N, Ferrer-Marin F, Hernandez L, Huerta-Aragones J, Leon A, Lopez-Duarte M, Lopez E, Martin-Salces M, Nomdedeu M, Ona R, Pelaez-Pleguezuelos I, Ramos F, Sebastian E, Serrano C, Sierra-Aisa C, Vidal-Laso R, Gonzalez-Porras JR, Lozano ML, Bastida JM, Rivera J. Insights into the clinical, platelet and genetic landscape of inherited thrombocytopenia with malignancy risk. Br J Haematol. 2025 Jul 16. doi: 10.1111/bjh.70001. Online ahead of print. PubMed PMID: 40670159.
AÑO: 2025; IF: 3.8
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Sanchez-Fuentes A, Perez-Botero J, Bastida JM, Rivera J. Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays. Biomolecules. 2025 Jun 10;15(6):846. doi: 10.3390/biom15060846. PubMed PMID: 40563486; PubMed Central PMCID: PMC12191158.
AÑO: 2025; IF: 4.8
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Arndt N, Falcinelli E, Zamora-Canovas A, Fuentes AS, Marin-Quilez A, Nieto-Hernandez MDM, Rivera J, Gresele P, Bury L. The co-inheritance of two ITGB3 variants with additive detrimental effects on platelets leads to variant Glanzmann thrombasthenia. Haematologica. 2025 Sep 25. doi: 10.3324/haematol.2025.288369. Online ahead of print. PubMed PMID: 40994361.
AÑO: 2025; IF: 7.9
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