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Successful immune tolerance in two children with severe haemophilia A

, et al. AntiBinhibitor coagulant complex prophylaxis in hemophilia with inhibitors. N Engl J Med 2011; 365: 1684B92. 8. MancoBJohnson MJ, Abshire TC, Schapiro AD, et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe haemophilia. N Engl J Med 2007; 357: 535B544. 9. Konkle BA, Ebbesen LS, Erhardtsen E, et al. Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in haemophilia patients with inhibitors. J Thromb Haemost 2007; 5: 1904B1913. 10. Hay

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Multiple joint procedures in haemophilia: benefit of self-reported activities

References 1. Ahlberg A. Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia A and B. Acta Orthopaedica Scandinavica 1965; 77 (suppl): 5-99. 2. De Kleijn P, Fischer K, Vogely CCh, Hendriks C, Lindeman E. In-hospital rehabilitation after multiple joint procedures of the lower extremities in haemophilia patients: clinical guidelines for physical therapists. Haemophilia 2011; 17: 971-8. 3. De Kleijn P, Sluiter D, Vogely CCh

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Does a patient’s personality style impact health outcomes?

-2834.2008.00918.x. 7. Towler J. Managing conflicts effectively: workplace conflict management and how to do it well. Available from: http://creativeorgdesign.com/article.htm?id=112&title=Managing_Conflicts_Effectively (accessed 9 April 2016). 8. Rodriguez-Merchan EC, Jimenez-Yuste V, Aznar JA, et al. Joint protection in haemophilia. Haemophilia 2011;17 Suppl 2:1-23. doi: 10.1111/j.1365-2516.2011.02615.x. 9. Skinner MW. WFH: closing the global gap -- achieving optimal care. Haemophilia 2012;18 Suppl 4:1-12. doi: 10.1111/j.1365

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UK physiotherapy and haemophilia: A future strategy built on past success

References 1. Manco-Johnson MJ, Abshire TC, Shapiro AD, Riske B, Hacker MR, Kilcoyne R, Ingram JD, Manco-Johnson ML, Funk S, Jacobson L, Valentino LA, Hoots WK, Buchanan GR, DiMichele D, Recht M, Brown D, Leissinger C, Bleak S, Cohen A, Mathew P, Matsunaga A, Medeiros D, Nugent D, Thomas GA, Thompson AA, McRedmond K, Soucie JM, Austin H, Evatt BL. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. N Engl J Med. 2007 Aug 9;357(6):535-44. 2. Jansen NW, Roosendaal G, Lafeber FP

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Endoscopic Diagnosis of Intramural Hematoma in The Colon sigmoideum In a Child With High Titer Inhibitory Hemophilia A

A, Midy D. Spontaneous intramural haematoma of the sig-moid colon causing acute intestinal obstruction in a haemophiliac: report of a case. Haemophilia 2008;14(2):383-4. 5. Parker S, Cobb CF, Spero JA, Van Thiel DH. Sig-moidovesicular fistula in a hemophiliac with diver-ticular disease. J Clin Gastroenterol 1986;8(4):461-5. 6. Kahn A, Vandenbogaert N, Cremer N, Fondu P. Intramural hematoma of the alimentary tract in two hemophilic children. Helv Paediatr Acta 1977; 31(6):503-7. 7. Harrison HC, Lord RS, Chesterman CN, Biggs JC, Tracy GD. Spontaneous

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Nurse-led telephone review service for mild inherited bleeding disorders improves attendance rates, frees hospital resources and is highly rated by patients

References 1. White GC, Rosendaal F, Aledort LM, et al. (2001) Definitions in haemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 2001; 85(3): 560. 2. The Haemophilia Alliance. A National Service Specification for Haemophilia and Related Conditions. London: The Haemophilia Alliance, 2006. Available at: http://www.ukhcdo.org/docs/HaemAlliance-NatSvsSpec2006.pdf (accessed

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Evaluation of a shortened course of tranexamic acid for patients with inherited bleeding disorders following dental procedures

recommendations. Haemophilia 2009; 15(3): 639-58. 12. British National Formulary, 2017. Available from http://www.medicinescomplete.com (accessed: 9 May 2017). 13. Nuvvula S, Gaddam KR, Kamatham R. Efficacy of tranexamic acid mouthwash as an alternative for factor replacement in gingival bleeding during dental scaling in cases of hemophilia: a randomized clinical trial. Contemp Clin Dent 2014; 5(1): 49-53. doi 10.4103/0976-237X.128663. 14. NHS Health Research Authority. Defining research, 2013. Available from: www

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Prevalence, pattern and clinical implications of transfusion transmissible viral infections among paediatric haemophiliacs in northern Nigeria

-2. doi: 10.5144/0256-4947.2012.200. 31. Borhany M, Shamsi T, Boota S, et al. Transfusion transmitted infections in patients with hemophilia of Karachi, Pakistan. Clin Appl Thromb Hemost 2011; 17: 651-5. doi: 10.1177/1076029611398122. 32. Makris M, Preston FE. Chronic hepatitis in haemophilia. Blood Rev 1993; 7: 243-50. doi: 10.1016/0268-960X(93)90011-R. 33. Heinz S, Braspenning J. Measurement of blood coagulation factor synthesis in cultures of human hepatocytes. Methods Mol Biol 2015; 1250: 309-16. doi: 10

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Evaluation of MixPro® among users and nurses

References 1 Cancio MI, Reiss UM, Nathwani AC, Davidoff AM, et al. Developments in the treatment of hemophilia B: focus on emerging gene therapy. Appl Clin Genet 2013; 6: 91-101. 2 Mannucci PM, Franchini M. Is haemophilia B less severe than haemophilia A? Haemophilia 2013; 19(4): 499-502. 3 Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, et al. Guidelines for the management of hemophilia. Haemophilia 2013; 19(1): e1-47. 4 Chalmers, A. Haemophilia A and B: disease differences and the use of

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Bleeding disorders in girls and women: setting the scene

REFERENCES 1. Noone D, Skouw-Rasmussen N, Lavin M, van Galen KPM, Kadir RA. Barriers and challenges faced by women with congenital bleeding disorders in Europe: Results of a patient survey conducted by the European Haemophilia Consortium. Haemophilia 2019; 25(3): 468-74. doi: 10.1111/hae.13722. 2. World Federation of Hemophilia. WFH Annual Report 2017. Available from http://www1.wfh.org/publications/files/pdf-1696.pdf (accessed 29 May 2019). 3. Jacobson AE, Vesely SK, Koch T, Campbell K, O’Brien SH. Patterns of von Willebrand disease

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