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5. Relation of factor VIII and IX inhibitors with ABO blood groups in 150 patients with haemophilia A and B. Torghabeh HM; Pourfathollah A; Shooshtari MM; Yazdi ZR Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):33-4. PubMed ID: 17242502 [TBL] [Abstract][Full Text] [Related]
6. Frequency of specific coagulation inhibitors and antiphospholipid antibodies in Tunisian haemophiliacs. Kraiem I; Hadhri S; El Omri H; Sassi R; Chaabani W; Ennabli S; Skouri H Ann Biol Clin (Paris); 2012; 70(6):659-65. PubMed ID: 23207810 [TBL] [Abstract][Full Text] [Related]
7. Immune tolerance induction with highly purified plasma-derived factor VIII containing von Willebrand factor in hemophilia A patients with high-responding inhibitors. Orsini F; Rotschild C; Beurrier P; Faradji A; Goudemand J; Polack B Haematologica; 2005 Sep; 90(9):1288-90. PubMed ID: 16154861 [TBL] [Abstract][Full Text] [Related]
8. Drug therapy reviews: clinical use of hemostatic agents. Lowe GD; Lawson DH Am J Hosp Pharm; 1978 Apr; 35(4):414-22. PubMed ID: 306196 [TBL] [Abstract][Full Text] [Related]
9. Prevalence of the intron 22 inversion of the factor VIII gene and inhibitor development in Polish patients with severe hemophilia A. Sawecka J; Skulimowska J; Windyga J; Lopaciuk S; Kościelak J Arch Immunol Ther Exp (Warsz); 2005; 53(4):352-6. PubMed ID: 16088320 [TBL] [Abstract][Full Text] [Related]
10. Experience with factor VIII: C inhibitors and acquired von Willebrand's disease in an adult at Ramathibodi Hospital. Angchaisuksiri P; Atichartakarn V; Pathepchotiwong K; Jootar S; Ungkanont A; Chuncharunee S Southeast Asian J Trop Med Public Health; 1993; 24 Suppl 1():152-8. PubMed ID: 7886560 [TBL] [Abstract][Full Text] [Related]
11. The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation. Hay CR; Brown S; Collins PW; Keeling DM; Liesner R Br J Haematol; 2006 Jun; 133(6):591-605. PubMed ID: 16704433 [TBL] [Abstract][Full Text] [Related]
12. [Acquired hemophilia caused by autoantibodies against factor VIII coagulation activity. Clinical, biological study and therapeutic indications. Experience based on a study of 9 cases]. Liozon E; Delaire L; Turlure P; Jaccard A; Loustaud-Ratti V; Réméniéras L; Julia A; Gaillard S; Bordessoule D; Vidal E Ann Med Interne (Paris); 1997; 148(7):477-90. PubMed ID: 9538386 [TBL] [Abstract][Full Text] [Related]
13. [Hemophiliacs with inhibitor. Experience at the Center of Medical Action for Hemophilia of the S. José Hospital]. Diniz MJ; Dias Francisco F; Tavares ML; Leal I Acta Med Port; 1992 Apr; 5(4):178-80. PubMed ID: 1605065 [TBL] [Abstract][Full Text] [Related]
14. The role of genetics in inhibitor formation. Gill JC Thromb Haemost; 1999 Aug; 82(2):500-4. PubMed ID: 10605742 [TBL] [Abstract][Full Text] [Related]
15. Laboratory identification of factor inhibitors: the perspective of a large tertiary hemophilia center. Kershaw G; Jayakodi D; Dunkley S Semin Thromb Hemost; 2009 Nov; 35(8):760-8. PubMed ID: 20169512 [TBL] [Abstract][Full Text] [Related]
16. Why do inhibitors develop? Principles of and factors influencing the risk for inhibitor development in haemophilia. Astermark J Haemophilia; 2006 Jul; 12 Suppl 3():52-60. PubMed ID: 16683997 [TBL] [Abstract][Full Text] [Related]
17. Properties of anti-factor VIII inhibitor antibodies in hemophilia A patients. Scandella DH Semin Thromb Hemost; 2000; 26(2):137-42. PubMed ID: 10919405 [TBL] [Abstract][Full Text] [Related]
19. Idiopathic factor VIII inhibitor autoantibody in a man presented after accident. Mansouritorghabeh H; Lak M; van Heerde WL Clin Appl Thromb Hemost; 2009 Oct; 15(5):588-90. PubMed ID: 18550586 [TBL] [Abstract][Full Text] [Related]
20. [Revision consensus hemophilia: treatment and responsibility. Nederlandse Vereniging van Hemophilia Patients]. Briët E; Mauser-Bunschoten EP Ned Tijdschr Geneeskd; 1997 Dec; 141(52):2566-71. PubMed ID: 9555158 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]