Haemophilia: Vol 20, No 2

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Haemophilia

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Haemophilia: Volume 20, Issue 2

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Editorial

Computational modelling and inhibitor risk: predicting the future?

Review Articles

Desmopressin (DDAVP) in the management of patients with congenital bleeding disorders

A review of evidence about behavioural and psychological aspects of chronic joint pain among people with haemophilia

Original Articles

Clinical haemophilia

In silico calculated affinity of FVIII-derived peptides for HLA class II alleles predicts inhibitor development in haemophilia A patients with missense mutations in the F8 gene

Influencing factors on the functional level of haemophilic patients assessed by FISH

The role of disease severity in influencing body mass index in people with haemophilia: a single-institutional cross-sectional study

Detection of bleeding disorders in Lebanon: outcomes of a pilot programme

Switching clotting factor concentrates: considerations in estimating the risk of immunogenicity

Assessment of pain threshold in haemophilic patients

Infection risk and stability of a continuous 8-h 250 mL rFVIII infusion

What should men living with haemophilia need to know? The perspectives of Canadian men with haemophilia

Pharmacokinetic analysis of anti-hemophilic factor in the obese patient

A study of prospective surveillance for inhibitors among persons with haemophilia in the United States

von Willebrand disease

An approach to outreach patients with von Willebrand disease in Egypt by targeting women with heavy menstrual bleeding and/or bleeding symptoms

Rare bleeding disorders

Bone cysts in patients with afibrinogenaemia: a literature review and two new cases

Platelet function defects in adolescents with heavy menstrual bleeding

Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines

Musculoskeletal

Integrated postural analysis in children with haemophilia

The clinical utility of bone turnover markers in the evaluation of bone disease in patients with haemophilia A and B

Long-term outcome of multiple joint procedures in haemophilia

Haemophilia Joint Health Score in healthy adults playing sports

Laboratory science

Characterization of F8 defects in haemophilia A in Pakistan: investigation of correlation between mutation type and the in vitro thrombin generation assay

Comparative field study evaluating the activity of recombinant factor VIII Fc fusion protein in plasma samples at clinical haemostasis laboratories

Review Article

Comprehensive management of chronic pain in haemophilia

Original Articles

Clinical haemophilia

Self-monitoring has potential for home exercise programmes in patients with haemophilia

Perceived challenges and attitudes to regimen and product selection from Italian haemophilia treaters: the 2013 AICE survey

Women with bleeding disorders

Severe and moderate haemophilia A and B in US females

Rare bleeding disorders

Changes in factor XIII level during pregnancy

Genetics

Characterization of four novel molecular changes in the promoter region of the factor VIII gene

Laboratory science

Factor IX oligomerization underlies reduced activity upon disruption of physiological conditions

Factor VIII assay mimicking in vivo coagulation conditions

Online Letters

Second-generation recombinant factor VIII and inhibitor risk: interpretation of RODIN study findings and implications for patients with haemophilia A

Making clinical decisions on the basis of RODIN

Lumbar puncture in haemophilia A: controversy in the management

Devastative tongue bleeding due to self-bite after dental extraction in a haemophilia A patient with inhibitor

Development of exogenous FVIII-specific inhibitor in a mild haemophilia patient with Glu272Lys mutation

Acute, symptomatic catheter-associated DVT with mobile, intra-cardiac thrombus in an infant with severe haemophilia A

Acquired haemophilia A after stem cell transplant for sickle cell disease: treatment with recombinant porcine factor VIII (OBI-1) and tolerance induction with rituximab/prednisone

Inhibitors to factor VII in congenital factor VII deficiency

A successful case of right hepatectomy in a patient with von Willebrand disease

Corrigendum

Corrigendum

This article corrects the following:

Correlation between endogenous VWF:Ag and PK parameters and bleeding frequency in severe haemophilia A subjects during three-times-weekly prophylaxis with rFVIII-FS

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