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The inhibitors – a challenge for the management of patients with hereditary haemophilia A

induction in patients with severe hemophilia with inhibitors: expert panel views and recommendations for clinical practice . Eur J Haematol. 2012; 88 :371-379. 7. ROCINO A., FRANCHINI M., COPPOLA A. Treatment and Prevention of Bleeds in Haemophilia Patients with Inhibitors to Factor VIII/IX . J Clin Med. 2017; 6 ;pii:E46. 8. ECKHARDT C.L., LOOMANS J.I., VAN VELZEN A.S., PETERS M., MAUSER-BUNSHOTEN E.P., SCHWAAB R., et al. Inhibitor development and mortality in non-severe hemophilia A . J Thromb Haemost. 2015; 13 :1217-1225. 9. FRANCHINI M., LIPPI G

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Fatality as a Feature of Medical Care

References 2. RAMOS-CASALS M, BRITO-ZERÓN P, LÓPEZ-GUILLERMO A, et al. Adult haemophagocytic syndrome. Lancet 2014; 383:1503. 3. CCOLLINS PW, HIRSCH S, BAGLIN TP, et al. Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation. Blood 2007; 109:1870. 4. HENTER JI, SAMUELSSON-HORNE A, ARICÓ M, et al. Treatment of hemophagocyticlymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. Blood 2002; 100

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Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease

; 103 (2):500–506. 52. MCMILLAN R. Antiplatelet antibodies in chronic immune thrombocytopenia and their role in platelet destruction and defective platelet production . Hematol Oncol Clin North Am. 2009; 23 (6):1163–1175. 53. NURDEN AT, FRESON K, SELIGSOHN U. Inherited platelet disorders Haemophilia. 2012; 18 (Suppl 4):154–60. 54. BALDUINI CL, PECCI A, SAVOIA A. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias . Br J Haematol. 2011; 154 (2):161–174. 55. BERNDT MC, ANDREWS RK. Bernard

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