Haemophilia: Vol 20, No 6

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Haemophilia: Volume 20, Issue 6

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Review Article

The burden and management of FXIII deficiency

Original Articles

Clinical haemophilia

Increased cancer risk in patients with haemophilia A: a nationwide population-based 14-year study in Taiwan

Similar bleeding phenotype in young children with haemophilia A or B: a cohort study

Parents of children with haemophilia at an early age: assessment of perceived stress and family functioning

Risk assessment for coronary heart disease in patients with haemophilia: a single centre study in the United States

Incidence and risk factors for inhibitor development in previously untreated severe haemophilia A patients born between 2005 and 2010

Patient data meta-analysis of Post-Authorization Safety Surveillance (PASS) studies of haemophilia A patients treated with rAHF-PFM

A pilot randomized control trial to evaluate the feasibility of an Internet-based self-management and transitional care program for youth with haemophilia

Validation of the Chinese version of the Canadian Haemophilia Outcomes-Kids' Life Assessment Tool (the CHO-KLAT)

Developing a two-sided intervention to facilitate shared decision-making in haemophilia: decision boxes for clinicians and patient decision aids for patients

The accuracy of a patient or parent-administered bleeding assessment tool administered in a paediatric haematology clinic

Physical activity and health outcomes in persons with haemophilia B

Impact of haemophilia with inhibitors on caregiver burden in the United States

Normal range of bleeding scores for the ISTH-BAT: adult and pediatric data from the merging project

Falling and fall risk factors in adults with haemophilia: an exploratory study

von Willebrand disease

Safety and efficacy of a von Willebrand factor/factor VIII concentrate (Wilate®): a single centre experience

Women with bleeding disorders

Prenatal diagnosis of haemophilia in Sweden now more commonly used for psychological preparation than termination of pregnancy

Genetics

Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations

Musculoskeletal

Effectiveness of an educational intervention of Physiotherapy in parents of children with haemophilia

Comparison of the effect of knee synovectomy in haemophilic patients with 153Sm- and 90Y -labelled hydroxyapatite 1 year after

Knee flexion contracture in haemophilia: treatment with circular external fixator

Impact of joint status on contraction steadiness of m. quadriceps femoris in people with severe haemophilia

Laboratory science

Recombinant factor IX: discrepancies between one-stage clotting and chromogenic assays

New quantitative aPTT waveform analysis and its application in laboratory management of haemophilia A patients

Native plasma-derived FVIII/VWF complex has lower sensitivity to FVIII inhibitors than the combination of isolated FVIII and VWF proteins. Impact on Bethesda assay titration of FVIII inhibitors

Genetics

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women

Prenatal diagnosis in haemophilia A: experience of the genetic diagnostic laboratory

Laboratory science

A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice

Online Letters

Successful treatment of non-invasive bladder tumour in a haemophilia A patient with high-responding inhibitors: a case report

Long-term treatment course of a patient with mild haemophilia A who developed a high titre factor VIII inhibitor

Thromboembolic incidence with transiently elevated levels of coagulation factors in patients with von Willebrand disease treated with VWF:FVIII concentrate during surgery

Are low-density lipoprotein receptor-related protein 1 or non-neutralizing antibodies predictors of FVIII in vivo recovery in haemophilia A patients?

The first case of int1h-related inversion in Japanese haemophilia A patients

Continuous infusion of human plasma-derived von Willebrand factor concentrate as an effective therapy in a patient with acquired von Willebrand disease

Adult haemophilia A patients with inhibitors: successful immune tolerance induction with a single FVIII/VWF product

Management of atrial fibrillation in people with haemophilia – a consensus view by the ADVANCE Working Group

Quantitative ultrasound and dual energy X-ray absorptiometry in the assessment of osteoporosis in patients with haemophilia

Thrombin generation in two FXI-deficient patients treated with Hemoleven®

Haemophilia A carriers demonstrate pathological and radiological evidence of structural joint changes

Development of anti-factor XIII antibodies in a patient with hereditary factor XIII deficiency receiving therapy for chronic hepatitis C

Multiple intraosseous pseudotumours of distal radius and hands in a patient with haemophilia A: case report

Combined FV and FVIII deficiency (F5F8D) in a Chinese family with a novel missense mutation in MCFD2 gene

Predicting early and delayed bleedings in children who undergo adeno-tonsillectomy surgery. Is it really possible?

Total elbow arthroplasty in patient with severe von Willebrand disease

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Safety and efficacy of a von Willebrand factor/factor VIII concentrate (Wilate^®): a single centre experience

Comparison of the effect of knee synovectomy in haemophilic patients with ¹⁵³Sm- and ⁹⁰Y -labelled hydroxyapatite 1 year after

Thrombin generation in two FXI-deficient patients treated with Hemoleven^®