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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 1
2012 1
2015 1
2016 3
2017 3
2018 3
2019 2
2020 3
2021 3
2022 2
2023 5
2024 0

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26 results

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Page 1
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.
Borràs N, Batlle J, Pérez-Rodríguez A, López-Fernández MF, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Balda I, Altisent C, Pérez-Montes R, Fisac RM, Iruín G, Herrero S, Soto I, de Rueda B, Jiménez-Yuste V, Alonso N, Vilariño D, Arija O, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Sarmiento L, Iñigo B, Nieto MDM, Vidal R, Martínez MP, Aguinaco R, César JM, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Cornudella R, Aguilar C, Vidal F, Corrales I. Borràs N, et al. Among authors: corrales i. Haematologica. 2017 Dec;102(12):2005-2014. doi: 10.3324/haematol.2017.168765. Epub 2017 Sep 29. Haematologica. 2017. PMID: 28971901 Free PMC article.
Earth: the planet of the annexins.
Martínez-González J, Corrales I. Martínez-González J, et al. Among authors: corrales i. Clin Investig Arterioscler. 2021 Jul-Aug;33(4):195-197. doi: 10.1016/j.arteri.2021.06.001. Clin Investig Arterioscler. 2021. PMID: 34274051 English, Spanish. No abstract available.
Update on Molecular Testing in von Willebrand Disease.
Batlle J, Pérez-Rodríguez A, Corrales I, Borràs N, Costa Pinto J, López-Fernández MF, Vidal F; PCM-EVW-ES Investigators Team. Batlle J, et al. Among authors: corrales i. Semin Thromb Hemost. 2019 Oct;45(7):708-719. doi: 10.1055/s-0039-1679922. Epub 2019 Apr 30. Semin Thromb Hemost. 2019. PMID: 31041796 Review.
Comparison of Extracellular Vesicle Isolation Methods for miRNA Sequencing.
Llorens-Revull M, Martínez-González B, Quer J, Esteban JI, Núñez-Moreno G, Mínguez P, Burgui I, Ramos-Ruíz R, Soria ME, Rico A, Riveiro-Barciela M, Sauleda S, Piron M, Corrales I, Borràs FE, Rodríguez-Frías F, Rando A, Ramírez-Serra C, Camós S, Domingo E, Bes M, Perales C, Costafreda MI. Llorens-Revull M, et al. Among authors: corrales i. Int J Mol Sci. 2023 Jul 29;24(15):12183. doi: 10.3390/ijms241512183. Int J Mol Sci. 2023. PMID: 37569568 Free PMC article.
Type 2N VWD: Conclusions from the Spanish PCM-EVW-ES project.
Pérez-Rodríguez A, Batlle J, Pinto JC, Corrales I, Borràs N, Garcia-Martínez I, Cid AR, Bonanad S, Parra R, Mingot-Castellano ME, Navarro N, Altisent C, Pérez-Montes R, Moretó A, Herrero S, Soto I, Mosteirín NF, Jiménez-Yuste V, Jacob AA, Fontanes E, Mateo J, Quismondo NC, Batlle F, Vidal F, López-Fernández MF; investigators and centers involved in the PCM-EVW-ES project. Pérez-Rodríguez A, et al. Among authors: corrales i. Haemophilia. 2021 Nov;27(6):1007-1021. doi: 10.1111/hae.14405. Epub 2021 Sep 7. Haemophilia. 2021. PMID: 34494337
First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.
Bandini P, Borràs N, Fernandez Mellid E, Martin-Fernandez L, Melero Valentín P, Comes N, Ramírez L, Cadahia Fernández P, Rodríguez Ruiz M, Perez Encinas MM, Vidal F, Corrales I. Bandini P, et al. Among authors: corrales i. Br J Haematol. 2023 Nov;203(4):e102-e107. doi: 10.1111/bjh.19050. Epub 2023 Sep 11. Br J Haematol. 2023. PMID: 37696499 No abstract available.
IX international curse of continuing formation in haemophilia and other congenital coagulopathies. The role of the Laboratory in coagulation disorders. Diagnosis of von Willebrand disease.
Batlle J, Pérez-Rodríguez A, Corrales I, Borràs N, Pinto JC, López-Fernández MF, Vidal F; on behalf PCM-EVW-ES Investigators Group. Batlle J, et al. Among authors: corrales i. Blood Coagul Fibrinolysis. 2022 Jan 1;33(Suppl 1):S12-S14. doi: 10.1097/MBC.0000000000001093. Blood Coagul Fibrinolysis. 2022. PMID: 34783692
26 results