Haemophilia: Vol 16, No 4

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Haemophilia

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Haemophilia: Volume 16, Issue 4

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Review Articles

A review of long-term prophylaxis in the rare inherited coagulation factor deficiencies

Bernard Soulier syndrome in pregnancy: a systematic review

Original Articles

Clinical haemophilia

Knowledge of disease and adherence in adult patients with haemophilia

Limited blood sampling for pharmacokinetic dose tailoring of FVIII in the prophylactic treatment of haemophilia A

Balance dysfunction in adults with haemophilia

Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE® in patients with von Willebrand’s disease: a prospective multi-centre study

Recombinant activated factor VII safety and efficacy in the treatment of cranial haemorrhage in patients with congenital haemophilia with inhibitors: an analysis of the Hemophilia and Thrombosis Research Society Registry (2004–2008)

Inhibitors

The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A

Musculoskeletal

Radioisotope synoviorthesis with Holmium-166-chitosan complex in haemophilic arthropathy

Haemophilic arthropathy of the ankle treated by total ankle replacement: a case series

Adolescence

Psychosocial correlates of physical activity in adolescents with haemophilia

Laboratory science

Laboratory identification of factor VIII inhibitors in the real world: the experience from Australasia

Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancy

Genetics

Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency

How we treat

How we treat: Haematuria in adults with haemophilia

Letters to the Editors

Pseudoaneurysm in association with a knee endoprothesis operation in an inhibitor-positive haemophilia A patient – treatment with local thrombin

Haemothorax in children with congenital coagulopathy

Acute myocardial infarction in a Chinese patient with haemophilia A and risk factors for coronary artery disease: a case report with autopsy

Molecular basis of factor X deficiency cases from India

Assessing baseline joint hypermobility as a risk factor for arthropathy development in moderate and severe haemophilia

Thrombin time and fibrinogen as initial screening tests for people with inherited bleeding disorders

Factor VIII/von Willebrand factor concentrate for treatment of life threatening epistaxis in Glanzmann’s thrombasthenia

Peri-interventional control of haemostasis in a patient with combined coagulation factor V- and factor VIII-deficiency and anaphylaxis to fresh frozen plasma – a rare indication for recombinant factor VIIa

Treatment of mantle cell lymphoma with autologous stem-cell transplantation in a patient with severe congenital haemophilia-A and chronic (B and C virus) hepatitis

Control of variceal bleeding in a patient with severe haemophilia A and factor VIII inhibitors using a transjugular intrahepatic portosystemic shunt

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Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE^® in patients with von Willebrand’s disease: a prospective multi-centre study