Haemophilia: Vol 16, No 6

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Haemophilia: Volume 16, Issue 6

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Review Articles

The ‘royal disease’– haemophilia A or B? A haematological mystery is finally solved

Towards comprehensive care in transition for young people with haemophilia

Muscle bleeds in professional athletes – diagnosis, classification, treatment and potential impact in patients with haemophilia

Original Articles

Clinical haemophilia

Postauthorization safety surveillance of ADVATE [antihaemophilic factor (recombinant), plasma/albumin-free method] demonstrates efficacy, safety and low-risk for immunogenicity in routine clinical practice

Functional characteristics of N8, a new recombinant FVIII

Paediatrics

A single centre experience in circumcision of haemophilia patients: Izmir protocol

Inhibitors

Domain specificity of factor VIII inhibitors during immune tolerance induction in patients with haemophilia A

Surgery in patients with haemophilia and high responding inhibitors: Izmir experience

Safety, pharmacokinetics and efficacy of factor VIIa formulated with PEGylated liposomes in haemophilia A patients with inhibitors to factor VIII – an open label, exploratory, cross-over, phase I/II study

Variability of thromboelastographic responses following the administration of rFVIIa to haemophilia A dogs supports the individualization of therapy with a global test of haemostasis

Musculoskeletal

Current practice in the management of muscle haematomas in patients with severe haemophilia

The effectiveness of radioisotope synovectomy for chronic synovitis in Turkish paediatric haemophiliacs: Ankara experience

Rare bleeding disorders

Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency

Dental disease in type 3 Von Willebrand disease: a neglected problem

Commentary

Human plasma-derived concentrates: preventing thrombosis and controlling haemorrhage

Letters to the Editors

Factors influencing haemophilia prevalence estimates from the volunteer-supervised Indian registry in Maharashtra

Awaiting evidence-based recommendations on prophylaxis in adult patients

Not a true tumour, but a renal pseudotumour: a case report of an 11.5 year old mild haemophilic child

Severe bleeding diathesis associated with moderate thrombocytopenia – diagnostic workup of seven family members with type 2B von Willebrand’s disease

Diffuse alveolar haemorrhage with severe haemophilia

Symptomatic carrier of haemophilia B Leyden: a case report

A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand’s disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation

Double mutations in haemophilia: muddling strangers or indifferent partners in crime?

Retraction

Retraction Statement for duplicate article HAE 2124: Mosaicism and haemophilia

Abstracts

Late Breaking Abstracts from the WFH Haemophilia 2010 World Congress

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