Haemophilia
The Official Journal of the World Federation of Hemophilia
Edited by:
C.A. Lee and C.M. Kessler
ISI Journal Citation Reports® Ranking: 2008: 32/62 Hematology
Impact Factor: 2.394
Why read or submit to Haemophilia?
- Publishes all articles regarding the comprehensive care of haemophilia
- EarlyView - articles appear online before the paper version is published! Click here to see the articles currently available
- Online submission via - http://mc.manuscriptcentral.com/hae
- European and North American based Editorial offices
Remember all Members of the WFH qualify for a discount of over 20% on the standard subscription rate!
TopNews and Announcements
XXIX International Congress of the World Federation of Hemophilia
10-14 July 2010, Buenos Aires, Argentina
View the conference website
Read the top downloaded articles from 2009 from the latest volume:
Haemophilia care then, now and in the future
J. Oldenburg, G. Dolan and G. Lemm
A systematic review of the cost-effectiveness of rFVIIa and APCC in the treatment of minor/moderate bleeding episodes for haemophilia patients with inhibitors
C. Knight, A. M. Danø, T. Kennedy-Martin
Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations
C. Hermans, C. Altisent, A. Batorova et al
Haemophilia care in children - benefits of early prophylaxis for inhibitor prevention
M. E. Mancuso, L. Graca, G. Auerswald and E. Santagostino
Paediatric haemophilia with inhibitors: existing management options, treatment gaps and unmet needs
E. Santagostino, M. Morfini, G. K. H. Auerswald et al
Challenges and controversies in haemophilia care in adulthood
G. Dolan, C. Hermans, R. Klamroth et al
Exercise and sport in the treatment of haemophilic patients: a systematic review
M. Gomis, F. Querol, J. E. Gallach et al
Haemophilia care in adolescents - compliance and lifestyle issues
P. Petrini and A. Seuser
Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven®] in elective orthopaedic surgery in haemophilic patients with inhibitors
P. L. F. Giangrande, J. T. Wilde and B. Madan et al
Online Content Now Available Back to Volume 1
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TopHighlights
Editor's choice
Selected content from Haemophilia
Pathogenesis of haemophilic arthropathy
G Roosendaal, FP Lafeber
Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies
JW Ironside
The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization
CA Lee, C Chi, SR Pavord et al.
Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment
CPM Hayward, AK Rao and M Cattaneo
Quality of life is associated to the orthopaedic status in haemophilic patients with inhibitors
Scalone L, Mantovani LG, Mannucci PM, et al.
Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A
EA Chalmers, SA Brown, D Keeling et al.
Rituximab for congenital haemophiliacs with inhibitors: a Canadian experience
M Carcao, M, St Louis J, Poon MC et al.
Cellular and genetic therapies for haemophilia
D Lillicrap, T Vandendriessche and K High
Congenital factor VII deficiency: therapy with recombinant activated factor VII - a critical appraisal
G Mariani, BA Konkle and J Ingerslev
Why do inhibitors develop? Principles of and factors influencing the risk for inhibitor development in haemophilia
J Astermark
