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A Case of Acquired Hemophilia A with Maxillary Osteitis

factor VIII hemophilia following influenza vaccination. Eur J Clin Pharmacol. 2010;66:1069-70. 5. Collins P, 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;109:1870-7. 6. Franchini M, Gandini G, Di Paolantonio T, Mariani G. Acquired hemophilia A: a concise review. Am J Hematol. 2005;80:55-63. 7. Hay CR, Negrier C, Ludlam CA. The treatment of bleeding in acquired hemophiliawith

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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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Multidiciplinary Treatment of a Haemophilic Person with Total Hip Replacement Surgery- A Case Report

References 1. Bossard D, Carrillon Y, Stieltjes N, Larbre J.P., Laurian Y, Molina V, Dirat G. Management of haemophilic arthropathy. Haemophilia. 2008;14(Suppl. 4):11-19. 2. Heijnen L, Dirat G, Chen L, Tulaar A.B.M., Moysisyan L., Nassar N.M.M., Batistella L.B. The role of the physiatrists in haemophilia comprehensive care team in different parts of the world. Haemophilia. 2008;14(Suppl.3):153-161. 3. Battistella LR. Multidisciplinary aspects of rehabilitation in developing countries. In Copmrehensive

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Congenital Factor V Deficiency: Moroccans Cases

haemorrhage during gestation. Haemophilia. 2007;13: 432-34. 9. Alcantara M, Ducastelle S, Rugeri L, Dargaud Y. Acquired factor V deficiency: A rare bleeding disorder with variable clinical presentations. Rev Med Intern. 2010;3976. 10. Huang JN, Koerper MA.Factor V deficiency: a concise review. Haemophilia. 2008;14:1164-9.

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Noninvasive Assessment of Coronary Arteries in Patients with Hematologic Disorders

-Scherrer A. Management of an acute coronary syndrome in a patient with severe haemophilia A. Haemophilia . 2007;13:763-765. 21. Girolami A, Ruzzon E, Fabris F, Varvarikis C, Sartori R, Girolami B. Myocardial Infarction and Other Arterial Occlusions in Hemophilia A Patients. Acta Haematol . 2006;116:120-125. 22. Spiel AO, Gilbert JC, Jilma B. Von Willebrand Factor in Cardiovascular Disease. Focus on Acute Coronary Syndromes. Circulation . 2008;117:1449-1459. 23. Schutgens RE, Tuinenburg A, Roosendaal G, Guyomi SH, Mauser-Bunschoten EP. Treatment of

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Molecular Diagnosis of Toxoplasmosis in Non Immune Pregnant Females

: a 4-year survey Clin Microbiol Infect. 2010;16(10):1594-602. 28. Hisada M, O'Brien TR, Rosenberg PS, Goedert JJ. Virus load and risk of heterosexual transmission of human immunodeficiency virus and hepatitis C virus by men with hemophilia. The Multicenter Hemophilia Cohort Study. J Infect Dis. 2000;181(4):1475-8. 29. Nimri L, Pelloux H, Elkhatib L. Detection of Toxoplasma gondii DNA and specific antibodies in high-risk pregnant women. Am J Trop Med Hyg. 2004;71(6):831-5. 30. Dupon M, Cazenave J, Pellegrin JL, Ragnaud

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Rendu-Osler-Weber Syndrome: A Case Report

(927): 18-24. 11. Abdalla SA, Letarte M. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease. J Med Genet. 2006; 43: 97-110. 12. Mahmoud M, Allinson KR, Zhai Z, et al. Pathogenesis of arteriovenous malformations in the absence of endoglin. Circ Res. 2010; 106:1425-33. 13. Sharathkmar AA, Shapiro A. Hereditary haemorrhagic telangiectasia. Haemophilia. 2008; 14: 1269-80. 14. Bossler, AD, Richards J, George C, Godmilow L, Ganguly A. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical

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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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