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51 results

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Page 1
Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A.
Eckhardt CL, van Velzen AS, Peters M, Astermark J, Brons PP, Castaman G, Cnossen MH, Dors N, Escuriola-Ettingshausen C, Hamulyak K, Hart DP, Hay CR, Haya S, van Heerde WL, Hermans C, Holmström M, Jimenez-Yuste V, Keenan RD, Klamroth R, Laros-van Gorkom BA, Leebeek FW, Liesner R, Mäkipernaa A, Male C, Mauser-Bunschoten E, Mazzucconi MG, McRae S, Meijer K, Mitchell M, Morfini M, Nijziel M, Oldenburg J, Peerlinck K, Petrini P, Platokouki H, Reitter-Pfoertner SE, Santagostino E, Schinco P, Smiers FJ, Siegmund B, Tagliaferri A, Yee TT, Kamphuisen PW, van der Bom JG, Fijnvandraat K; INSIGHT Study Group. Eckhardt CL, et al. Among authors: haya s. Blood. 2013 Sep 12;122(11):1954-62. doi: 10.1182/blood-2013-02-483263. Epub 2013 Aug 7. Blood. 2013. PMID: 23926300 Free article.
Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations.
Loomans JI, van Velzen AS, Eckhardt CL, Peters M, Mäkipernaa A, Holmstrom M, Brons PP, Dors N, Haya S, Voorberg J, van der Bom JG, Fijnvandraat K. Loomans JI, et al. Among authors: haya s. J Thromb Haemost. 2017 Feb;15(2):246-254. doi: 10.1111/jth.13581. Epub 2017 Feb 3. J Thromb Haemost. 2017. PMID: 27943580 Free article.
Mortality caused by intracranial bleeding in non-severe hemophilia A patients.
Loomans JI, Eckhardt CL, Reitter-Pfoertner SE, Holmström M, van Gorkom BL, Leebeek FWG, Santoro C, Haya S, Meijer K, Nijziel MR, van der Bom JG, Fijnvandraat K. Loomans JI, et al. Among authors: haya s. J Thromb Haemost. 2017 Jun;15(6):1115-1122. doi: 10.1111/jth.13693. Epub 2017 May 4. J Thromb Haemost. 2017. PMID: 28374963 Free article.
Management of acquired hemophilia A: results from the Spanish registry.
Mingot-Castellano ME, Pardos-Gea J, Haya S, Bastida-Bermejo JM, Tàssies D, Marco-Rico A, Núñez R, García-Candel F, de Mora MF, Soto I, Álvarez-Román MT, Asenjo S, Carrasco M, Lluch-García R, Martín-Antorán JM, Rodríguez-Alén A, Roselló E, Torres-Miñana L, Marcellini-Antonio S, Moretó-Quinana A, Rodríguez-García JA, Aguinaco-Culebras R, Alonso-Escobar N, Cervero-Santiago C, Fernández-Mosteirín N, Martínez-Badás MP, Pérez-Sánchez M, Pérez-Montes R, Rodríguez-González R, Uribe-Barrientos M, Caparrós-Miranda IS, Iglesias-Fernández M, Baena Á, Rodríguez-López M, Sebrango-Sandia A, Vázquez-Fernández I, Marco P; Acquired Haemophilia Spanish Registry of the Spanish Society of ThrombosisHaemostasis (SETH). Mingot-Castellano ME, et al. Among authors: haya s. Blood Adv. 2021 Oct 12;5(19):3821-3829. doi: 10.1182/bloodadvances.2021004626. Blood Adv. 2021. PMID: 34521101 Free PMC article.
Efficacy and safety evaluation of Fanhdi® , a plasma-derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures: A prospective clinical study.
Jimenez-Yuste V, Núñez L, Alvarez-Roman MT, Martin-Salces M, Haya S, Federici AB, Grifols C, Mairal E, Torres M, Páez A. Jimenez-Yuste V, et al. Among authors: haya s. Haemophilia. 2022 Jan;28(1):e23-e27. doi: 10.1111/hae.14453. Epub 2021 Nov 4. Haemophilia. 2022. PMID: 34735040 Free PMC article. No abstract available.
51 results