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A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor.
Jacquemin M, Lavend'homme R, Benhida A, Vanzieleghem B, d'Oiron R, Lavergne JM, Brackmann HH, Schwaab R, VandenDriessche T, Chuah MK, Hoylaerts M, Gilles JG, Peerlinck K, Vermylen J, Saint-Remy JM. Jacquemin M, et al. Among authors: peerlinck k. Blood. 2000 Aug 1;96(3):958-65. Blood. 2000. PMID: 10910910 Free article.
Molecular mechanisms of mild and moderate hemophilia A.
Jacquemin M, De Maeyer M, D'Oiron R, Lavend'Homme R, Peerlinck K, Saint-Remy JM. Jacquemin M, et al. Among authors: peerlinck k. J Thromb Haemost. 2003 Mar;1(3):456-63. doi: 10.1046/j.1538-7836.2003.00088.x. J Thromb Haemost. 2003. PMID: 12871450 Free article. Review.
The addition of idarucizumab to plasma samples containing dabigatran allows the use of routine coagulation assays for the diagnosis of hemostasis disorders.
Jacquemin M, Toelen J, Schoeters J, van Horenbeeck I, Vanlinthout I, Debasse M, Peetermans M, Vanassche T, Peerlinck K, van Ryn J, Verhamme P. Jacquemin M, et al. Among authors: peerlinck k. J Thromb Haemost. 2015 Nov;13(11):2087-92. doi: 10.1111/jth.13138. Epub 2015 Oct 5. J Thromb Haemost. 2015. PMID: 26347330 Free article.
The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia.
Jacquemin M, Vanlinthout I, Van Horenbeeck I, Debasse M, Toelen J, Schoeters J, Lavend'homme R, Freson K, Peerlinck K. Jacquemin M, et al. Among authors: peerlinck k. Int J Lab Hematol. 2017 Jun;39(3):301-307. doi: 10.1111/ijlh.12625. Epub 2017 Mar 20. Int J Lab Hematol. 2017. PMID: 28318107 Clinical Trial.
191 results