Works matching IS 13518216 AND DT 2015 AND VI 21 AND IP 1
Results: 47
Comprehensive evaluation of haemostatic function in von Willebrand disease patients using a microchip-based flow chamber system.
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- Haemophilia, 2015, v. 21, n. 1, p. 71, doi. 10.1111/hae.12610
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Wilate use in 47 children with von Willebrand disease: the North London paediatric haemophilia network experience.
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- Haemophilia, 2015, v. 21, n. 1, p. e44, doi. 10.1111/hae.12497
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Are there systemic comorbidities in haemophilia unrelated to bleeding and transfusion-transmitted infections?
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- Haemophilia, 2015, v. 21, n. 1, p. e83, doi. 10.1111/hae.12560
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Human parvovirus 4 in Brazilian patients with haemophilia, beta-thalassaemia major and volunteer blood donors.
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- Haemophilia, 2015, v. 21, n. 1, p. e86, doi. 10.1111/hae.12564
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A case-control study assessing bone mineral density in severe haemophilia A in the UK.
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- Haemophilia, 2015, v. 21, n. 1, p. 109, doi. 10.1111/hae.12565
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Acquired von Willebrand syndrome in paediatric patients with congenital heart disease: challenges in the diagnosis and management of this rare condition.
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- Haemophilia, 2015, v. 21, n. 1, p. e89, doi. 10.1111/hae.12567
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Postpartum von Willebrand factor levels in women with and without von Willebrand disease and implications for prophylaxis.
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- Haemophilia, 2015, v. 21, n. 1, p. 81, doi. 10.1111/hae.12568
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Hepatitis B vaccination is effective by subcutaneous route in children with bleeding disorders: a universal data collection database analysis.
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- Haemophilia, 2015, v. 21, n. 1, p. e39, doi. 10.1111/hae.12569
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Prospective evaluation of venous access difficulty and a near-infrared vein visualizer at four French haemophilia treatment centres.
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- Haemophilia, 2015, v. 21, n. 1, p. 21, doi. 10.1111/hae.12513
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Batch recall of French plasma-derived products due to variant Creutzfeldt-Jakob disease risk: the psychological impact on haemophilic patients, changes in their therapeutic demands and behaviour and ethical considerations.
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- Haemophilia, 2015, v. 21, n. 1, p. 27, doi. 10.1111/hae.12515
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Safety and efficacy of turoctocog alfa (NovoEight<sup>®</sup>) during surgery in patients with haemophilia A: results from the multinational guardian<sup>™</sup> clinical trials.
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- Haemophilia, 2015, v. 21, n. 1, p. 34, doi. 10.1111/hae.12518
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Management of pregnancy in type 2B von Willebrand disease: case report and literature review.
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- Haemophilia, 2015, v. 21, n. 1, p. e98, doi. 10.1111/hae.12580
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Cryotherapy for acute haemarthrosis in haemophilia - attempts to understand the 'ice age' practice.
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- Haemophilia, 2015, v. 21, n. 1, p. e103, doi. 10.1111/hae.12581
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Ankle joint-preserving surgery in a patient with severe haemophilia and Noonan syndrome: case report and literature review.
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- Haemophilia, 2015, v. 21, n. 1, p. e105, doi. 10.1111/hae.12583
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Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis.
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- Haemophilia, 2015, v. 21, n. 1, p. e108, doi. 10.1111/hae.12584
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Bleeding phenotype in carriers of haemophilia A does not correlate with thrombin generation.
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- Haemophilia, 2015, v. 21, n. 1, p. e111, doi. 10.1111/hae.12585
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Limits of agreement between raters are required for the use of HJHS 2.1 in clinical studies.
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- Haemophilia, 2015, v. 21, n. 1, p. e70, doi. 10.1111/hae.12586
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Response to 'limits of agreement between raters are required for use of HJHS 2.1 in clinical studies'.
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- Haemophilia, 2015, v. 21, n. 1, p. e71, doi. 10.1111/hae.12587
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- Article
Is it congenital or acquired von Willebrands disease?
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- Haemophilia, 2015, v. 21, n. 1, p. e113, doi. 10.1111/hae.12588
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Successful use of recombinant factor VIIa in a patient with acquired Glanzmann thrombasthenia.
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- Haemophilia, 2015, v. 21, n. 1, p. e116, doi. 10.1111/hae.12589
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Continuous infusion of recombinant factor VIII formulated with sucrose in surgery: Non-interventional, observational study in patients with severe haemophilia A.
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- Haemophilia, 2015, v. 21, n. 1, p. e19, doi. 10.1111/hae.12530
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The biological efficacy profile of BAX 855, a PEGylated recombinant factor VIII molecule.
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- Haemophilia, 2015, v. 21, n. 1, p. 58, doi. 10.1111/hae.12532
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Adherence to prophylaxis is associated with better outcomes in moderate and severe haemophilia: results of a patient survey.
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- Haemophilia, 2015, v. 21, n. 1, p. 64, doi. 10.1111/hae.12533
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Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay.
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- Haemophilia, 2015, v. 21, n. 1, p. 140, doi. 10.1111/hae.12536
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External fixators for open fractures of tibia and fibula in patients with haemophilia A.
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- Haemophilia, 2015, v. 21, n. 1, p. e51, doi. 10.1111/hae.12538
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USPIO-related T1 and T2 mapping MRI of cartilage in a rabbit model of blood-induced arthritis: a pilot study.
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- Haemophilia, 2015, v. 21, n. 1, p. e59, doi. 10.1111/hae.12601
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Research in haemophilia B - approaching the request for high evidence levels in a rare disease.
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- Haemophilia, 2015, v. 21, n. 1, p. 4, doi. 10.1111/hae.12603
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Thromboelastography identifies children with rare bleeding disorders and predicts bleeding phenotype.
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- Haemophilia, 2015, v. 21, n. 1, p. 124, doi. 10.1111/hae.12481
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Bone disease in patients with haemophilia A and B - where are we now?
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- Haemophilia, 2015, v. 21, n. 1, p. 1, doi. 10.1111/hae.12551
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Factor VIII inhibitory antibody in a patient with combined factor V/factor VIII deficiency.
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- Haemophilia, 2015, v. 21, n. 1, p. e77, doi. 10.1111/hae.12557
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A cystic focus filled with soft tissue in femoral head from a haemophilic arthropathy patient: a case report from China.
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- Haemophilia, 2015, v. 21, n. 1, p. e80, doi. 10.1111/hae.12559
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Development of haemophilic arthropathy of the ankle: results of a Delphi consensus survey on potential contributory factors.
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- Haemophilia, 2015, v. 21, n. 1, p. 116, doi. 10.1111/hae.12500
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Uneventful long-term anticoagulation with fluindione in a patient with severe factor XI deficiency.
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- Haemophilia, 2015, v. 21, n. 1, p. e72, doi. 10.1111/hae.12502
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Pharmacokinetics and safety of plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.
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- Haemophilia, 2015, v. 21, n. 1, p. 95, doi. 10.1111/hae.12505
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Thrombosis of abdominal aorta in congenital afibrinogenemia: case report and review of literature.
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- Haemophilia, 2015, v. 21, n. 1, p. 88, doi. 10.1111/hae.12507
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Light-chain amyloidosis presenting as a change in bleeding phenotype in a patient with mild haemophilia A.
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- Haemophilia, 2015, v. 21, n. 1, p. e92, doi. 10.1111/hae.12572
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Favourable impact of regular swimming in young people with haemophilia: experience derived from 'Desafio del Caribe' project.
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- Haemophilia, 2015, v. 21, n. 1, p. e12, doi. 10.1111/hae.12576
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Haemarthrosis and arthropathy do not favour the development of factor VIII inhibitors in severe haemophilia A mice.
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- Haemophilia, 2015, v. 21, n. 1, p. e94, doi. 10.1111/hae.12579
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Immune responses to human factor IX in haemophilia B mice of different genetic backgrounds are distinct and modified by TLR4.
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- Haemophilia, 2015, v. 21, n. 1, p. 133, doi. 10.1111/hae.12522
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Efficacy and safety of prophylactic treatment with plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.
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- Haemophilia, 2015, v. 21, n. 1, p. 102, doi. 10.1111/hae.12524
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Managing chronic pain in adults with haemophilia: current status and call to action.
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- Haemophilia, 2015, v. 21, n. 1, p. 41, doi. 10.1111/hae.12526
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A national survey of immunosuppression strategies for acquired haemophilia A.
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- Haemophilia, 2015, v. 21, n. 1, p. e73, doi. 10.1111/hae.12547
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Neonatal circumcision in severe haemophilia: a survey of paediatric haematologists at United States Hemophilia Treatment Centers.
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- Haemophilia, 2015, v. 21, n. 1, p. 52, doi. 10.1111/hae.12528
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The use of recombinant factor XIII in a major bleeding episode of a patient with congenital factor XIII deficiency - the first experience.
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- Haemophilia, 2015, v. 21, n. 1, p. e118, doi. 10.1111/hae.12591
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Cementless total hip arthroplasty for haemophilic arthropathy: follow-up result of more than 10 years.
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- Haemophilia, 2015, v. 21, n. 1, p. e54, doi. 10.1111/hae.12544
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Haemophilia Experiences, Results and Opportunities ( HERO) study: treatment-related characteristics of the population.
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- Haemophilia, 2015, v. 21, n. 1, p. e26, doi. 10.1111/hae.12545
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Long-term follow up of HIV-1-infected Korean haemophiliacs, after infection from a common source of virus.
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- Haemophilia, 2015, v. 21, n. 1, p. e1, doi. 10.1111/hae.12527
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- Article