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Hamostaseologie 2017; 37(02): 93-95
DOI: 10.1055/s-0037-1608913
DOI: 10.1055/s-0037-1608913
Editorial
Hemophilia in focus
World Hemophilia Day 2017Further Information
Publication History
Received and accepted: 18 April 2017
Publication Date:
20 November 2017 (online)
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References
- 1 World Federation of Hemophilia. World Hemophilia Day 2017. www.wfh.org.
- 2 International Society on Thrombosis and Haemostasis. World Haemophilia Day 2017. www.isth.org.
- 3 Deutscher Bundestag. Kalender 2017: Auswahl historischer Jahrestage sowie alljährlich wiederkehrender Gedenk-, Aktions- und Thementage. Wiss. Dienst 1: 3010–035/16. www.bundestag.de.
- 4 Peyvandi F, Mannucci PM, Garagiola I. et al. A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A. N Engl J Med 2016; 374: 2054-2064.
- 5 Shima M, Hanabusa H, Taki M. et al. Factor VIIIMimetic Function of Humanized Bispecific Antibody in Hemophilia A. N Engl J Med 2016; 374: 2044-2053.
- 6 Scharf RE. Alloantibodies to therapeutic FVIII and the use of emicizumab in hemophilia A. Hamostaseologie 2016; 36: 195-198.
- 7 Rehm H, Schmolders J, Koob S. et al. Falling and fall risk in adult patients with severe haemophilia. Hamostaseologie 2017; 37: 97-103.
- 8 van Vulpen LF, Schutgens RE, Coeleveld K. et al. IL-1beta, in contrast to TNFalpha, is pivotal in blood-induced cartilage damage and is a potential target for therapy. Blood 2015; 126: 2239-2246.
- 9 Srivastava A. Inflammation is key to hemophilic arthropathy. Blood 2015; 126: 2175-2176.
- 10 Wharton R, Austin S, Back D. Subchondral haematoma. The missing link in understanding haemophilic arthropathy?. Hamostaseologie 2017; 37: 104-106.
- 11 Sondermann J, Herbsleb M, Stanek F-D. et al. Health promotion for young patients with haemophilia. Hamostaseologie 2017; 37: 107-116.
- 12 Lechner H, Schleiermacher A, Berger K. et al. Wishes and worries of haemophilia patients. A patient survey from Bavaria. Hamostaseologie 2017; 37: 117-126.
- 13 Wiegand J, Schiefke I, Stein K. et al. Interferon-free treatment of chronic hepatitis C virus infection in patients with inherited bleeding disorders. Hamostaseologie 2017; 37: 127-130.
- 14 Teixeira L, Saavedra V, Sousa Santos B, Ferreira C. Portuguese Haemophilia Registry. Set of variables for computerized solution. Hamostaseologie 2017; 37: 131-137.
- 15 Mannhalter C. New developments in molecular biological diagnostics. Hamostaseologie 2017; 37: 138-151.
Correspondence to:
Univ.-Prof. Dr. Rüdiger E. Scharf, F.A.H.A.
Email: scharf@uni-duesseldorf.de
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References
- 1 World Federation of Hemophilia. World Hemophilia Day 2017. www.wfh.org.
- 2 International Society on Thrombosis and Haemostasis. World Haemophilia Day 2017. www.isth.org.
- 3 Deutscher Bundestag. Kalender 2017: Auswahl historischer Jahrestage sowie alljährlich wiederkehrender Gedenk-, Aktions- und Thementage. Wiss. Dienst 1: 3010–035/16. www.bundestag.de.
- 4 Peyvandi F, Mannucci PM, Garagiola I. et al. A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A. N Engl J Med 2016; 374: 2054-2064.
- 5 Shima M, Hanabusa H, Taki M. et al. Factor VIIIMimetic Function of Humanized Bispecific Antibody in Hemophilia A. N Engl J Med 2016; 374: 2044-2053.
- 6 Scharf RE. Alloantibodies to therapeutic FVIII and the use of emicizumab in hemophilia A. Hamostaseologie 2016; 36: 195-198.
- 7 Rehm H, Schmolders J, Koob S. et al. Falling and fall risk in adult patients with severe haemophilia. Hamostaseologie 2017; 37: 97-103.
- 8 van Vulpen LF, Schutgens RE, Coeleveld K. et al. IL-1beta, in contrast to TNFalpha, is pivotal in blood-induced cartilage damage and is a potential target for therapy. Blood 2015; 126: 2239-2246.
- 9 Srivastava A. Inflammation is key to hemophilic arthropathy. Blood 2015; 126: 2175-2176.
- 10 Wharton R, Austin S, Back D. Subchondral haematoma. The missing link in understanding haemophilic arthropathy?. Hamostaseologie 2017; 37: 104-106.
- 11 Sondermann J, Herbsleb M, Stanek F-D. et al. Health promotion for young patients with haemophilia. Hamostaseologie 2017; 37: 107-116.
- 12 Lechner H, Schleiermacher A, Berger K. et al. Wishes and worries of haemophilia patients. A patient survey from Bavaria. Hamostaseologie 2017; 37: 117-126.
- 13 Wiegand J, Schiefke I, Stein K. et al. Interferon-free treatment of chronic hepatitis C virus infection in patients with inherited bleeding disorders. Hamostaseologie 2017; 37: 127-130.
- 14 Teixeira L, Saavedra V, Sousa Santos B, Ferreira C. Portuguese Haemophilia Registry. Set of variables for computerized solution. Hamostaseologie 2017; 37: 131-137.
- 15 Mannhalter C. New developments in molecular biological diagnostics. Hamostaseologie 2017; 37: 138-151.