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423 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: leebeek fw. 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.
Effectiveness of managing suspected pulmonary embolism using an algorithm combining clinical probability, D-dimer testing, and computed tomography.
van Belle A, Büller HR, Huisman MV, Huisman PM, Kaasjager K, Kamphuisen PW, Kramer MH, Kruip MJ, Kwakkel-van Erp JM, Leebeek FW, Nijkeuter M, Prins MH, Sohne M, Tick LW; Christopher Study Investigators. van Belle A, et al. Among authors: leebeek fw. JAMA. 2006 Jan 11;295(2):172-9. doi: 10.1001/jama.295.2.172. JAMA. 2006. PMID: 16403929
[The new oral anticoagulant in the Netherlands].
Leebeek FW, Kamphuisen PW. Leebeek FW, et al. Ned Tijdschr Geneeskd. 2009 Apr 18;153(16):773-7. Ned Tijdschr Geneeskd. 2009. PMID: 19469152 Dutch. No abstract available.
Impaired fibrinolysis as a risk factor for Budd-Chiari syndrome.
Hoekstra J, Guimarães AH, Leebeek FW, Darwish Murad S, Malfliet JJ, Plessier A, Hernandez-Guerra M, Langlet P, Elias E, Trebicka J, Primignani M, Garcia-Pagan JC, Valla DC, Rijken DC, Janssen HL; European Network for Vascular Disorders of the Liver (EN-Vie). Hoekstra J, et al. Among authors: leebeek fw. Blood. 2010 Jan 14;115(2):388-95. doi: 10.1182/blood-2009-03-211557. Epub 2009 Nov 18. Blood. 2010. PMID: 19965669 Free article.
The JAK2 46/1 haplotype in Budd-Chiari syndrome and portal vein thrombosis.
Smalberg JH, Koehler E, Darwish Murad S, Plessier A, Seijo S, Trebicka J, Primignani M, de Maat MP, Garcia-Pagan JC, Valla DC, Janssen HL, Leebeek FW; European Network for Vascular Disorders of the Liver (EN-Vie). Smalberg JH, et al. Among authors: leebeek fw. Blood. 2011 Apr 14;117(15):3968-73. doi: 10.1182/blood-2010-11-319087. Epub 2011 Mar 1. Blood. 2011. PMID: 21364191 Free article.
423 results