Haemophilia: Vol 18, No 6

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Haemophilia

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Haemophilia: Volume 18, Issue 6

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Commemorative Article

Judith Graham Pool and the discovery of cryoprecipitate

Review Articles

Opinions on radiosynovectomy for chronic haemophilic synovitis: point/counterpoint

The effect of cooling on coagulation and haemostasis: Should “Ice” be part of treatment of acute haemarthrosis in haemophilia?

Original Articles

Clinical haemophilia

Registry of Hemophilia and other bleeding disorders in Syria

Daily dosing prophylaxis for haemophilia: a randomized crossover pilot study evaluating feasibility and efficacy

Determinants of participation in patients with severe haemophilia

Prevalence of depression in adults with haemophilia

The development of a patient partnership programme and its impact on quality improvements in a comprehensive haemophilia care service

Pharmacokinetic properties of IB1001, an investigational recombinant factor IX, in patients with haemophilia B: repeat pharmacokinetic evaluation and sialylation analysis

Paediatrics

Medical radiation exposure in children with bleeding disorders: an institutional experience

Effect of a self-help program for mothers of hemophilic children in Korea

The impact of sport on children with haemophilia

Feasibility of short message service to document bleeding episodes in children with haemophilia

Laboratory science

Feasibility of using thrombin generation assay (TGA) for monitoring of haemostasis during supplementation therapy in haemophilic patients without inhibitors

The fraction of recombinant factor VIII:Ag unable to bind von Willebrand factor has no FVIII coagulant activity: studies in vitro

Evaluation of a novel flow chamber system to assess clot formation in factor VIII-deficient mouse and anti-factor IXa-treated human blood

Genetics

Analysis of F9 point mutations and their correlation to severity of haemophilia B disease

Pharmacokinetics and pharmacodynamics of turoctocog alfa and N8-GP in haemophilia A dogs

Musculoskeletal

Ankle muscle activation in people with haemophilia

Peripheral quantitative computed tomography (pQCT) reveals alterations in the three-dimensional bone structure in children with haemophilia

An MRI scale for assessment of haemophilic arthropathy from the International Prophylaxis Study Group

Inhibitors

Multidisciplinary management of patients with haemophilia with inhibitors undergoing surgery in the United States: perspectives and best practices derived from experienced treatment centres

Kinetics of the interaction between anti-FVIII antibodies and FVIII from therapeutic concentrates, with and without von Willebrand factor, assessed by surface plasmon resonance

Dosing and effectiveness of recombinant activated factor VII (rFVIIA) in congenital haemophilia with inhibitors by bleed type and location: the experience of the Haemophilia and Thrombosis Research Society (HTRS) Registry (2004–2008)

Experience of recombinant activated factor VII usage during surgery in patients with haemophilia with inhibitors

Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A

Mutation spectrum and inhibitor risk in 100 Korean patients with severe haemophilia A

Announcement

6th Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) 6–8 February 2013, Warsaw, Poland

Online Letters

Reply to von Willebrand's disease and postpartum haemorrhage by Chee et al

Regional registry of bleeding disorders in Tunisia

A Canadian survey of self-infusion practices in persons with haemophilia A

Trauma-related bleeding complications in South African patients with haemophilia

Large psoas haematoma and femoral neuropathy in a patient with type 2B von Willebrand's disease

Analyses of recombinant activated factor VII treatments from clinical practice for rapid bleeding and acute pain control in haemophilia patients with inhibitors

Factor VIII inhibitors in patients with congenital severe haemophilia A and its relation to genotype

Arthroscopic synovectomy of the elbow covered with rFVIIa in a haemophilia B juvenile with inhibitor

Immune system polymorphisms and factor VIII inhibitor formation in Brazilian haemophilia A severe patients

Joint distraction: a treatment to consider for haemophilic arthropathy

Spectrum of F8 gene mutations in haemophilia A patients from Slovenia

Pattern of bleeding and response to therapy in Glanzmann thrombasthenia

Corrigendum

Corrigendum

This article corrects the following:

Predictors of treatment difficulties and satisfaction with haemophilia therapy in adult patients

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