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28. The use of factor VIII/von Willebrand factor concentrate for immune tolerance induction in haemophilia A patients with high-titre inhibitors: association of clinical outcome with inhibitor epitope profile. Greninger DA, Saint-Remy JM, Jacquemin M, Benhida A, DiMichele DM. Haemophilia; 2008 Mar; 14(2):295-302. PubMed ID: 18081826 [Abstract] [Full Text] [Related]
29. [Immunosuppressive treatment of a spontaneous inhibitor hemophilia A using cyclophosphamide, vincristine and prednisone following prior Factor VIII stimulation]. Dürig J, de Wit M, Fiedler W, Marx G, Hossfeld DK. Schweiz Med Wochenschr; 1996 Nov 23; 126(47):2026-31. PubMed ID: 8984611 [Abstract] [Full Text] [Related]
33. Von Willebrand factor-specific antibodies developing upon treatment of FVIII-deficient mice with different FVIII preparations. Kallas A, Kuuse S, Maimets T, Pooga M. Acta Haematol; 2008 Nov 23; 119(4):244-7. PubMed ID: 18594135 [No Abstract] [Full Text] [Related]
35. Recombinant FVIIa in the treatment of bleeding in acquired hemophilia. Guerin V, Chossat I, Dutronc H, Dubreuil M, Valentin F. Am J Hematol; 2002 Aug 23; 70(4):333. PubMed ID: 12210820 [No Abstract] [Full Text] [Related]
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37. Switching to low dose of plasma-derived factor VIII/vWF concentrates with Confact(®) -F as salvage immune tolerance induction in haemophilia A patients with inhibitors: five case reports from Japan. Nagao A, Oka T, Hanabusa H. Haemophilia; 2015 Sep 23; 21(5):e425-7. PubMed ID: 25996457 [No Abstract] [Full Text] [Related]
40. Immune tolerance induction with high von Willebrand factor/factor VIII content ratio concentrate in children with haemophilia A and high-responding inhibitor. Platokouki H, Pergantou H, Xafaki P, Komitopoulou A, Aronis S. Haemophilia; 2009 Mar 23; 15(2):617-9. PubMed ID: 19175417 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]