Works matching IS 13518216 AND DT 2012 AND VI 18
Results: 334
Ankle muscle activation in people with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 948, doi. 10.1111/j.1365-2516.2012.02852.x
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- Article
Pattern of bleeding and response to therapy in Glanzmann thrombasthenia.
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- Haemophilia, 2012, v. 18, n. 6, p. e423, doi. 10.1111/hae.12017
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Prevalence of depression in adults with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 868, doi. 10.1111/j.1365-2516.2012.02863.x
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Opinions on radiosynovectomy for chronic haemophilic synovitis: point/counterpoint.
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- Haemophilia, 2012, v. 18, n. 6, p. 836, doi. 10.1111/j.1365-2516.2012.02908.x
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The development of a patient partnership programme and its impact on quality improvements in a comprehensive haemophilia care service.
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- Haemophilia, 2012, v. 18, n. 6, p. 875, doi. 10.1111/j.1365-2516.2012.02885.x
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Pharmacokinetics and pharmacodynamics of turoctocog alfa and N8- GP in haemophilia A dogs.
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- Haemophilia, 2012, v. 18, n. 6, p. 941, doi. 10.1111/j.1365-2516.2012.02896.x
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Evaluation of a novel flow chamber system to assess clot formation in factor VIII-deficient mouse and anti-factor IXa-treated human blood.
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- Haemophilia, 2012, v. 18, n. 6, p. 926, doi. 10.1111/j.1365-2516.2012.02867.x
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Feasibility of using thrombin generation assay ( TGA) for monitoring of haemostasis during supplementation therapy in haemophilic patients without inhibitors.
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- Haemophilia, 2012, v. 18, n. 6, p. 911, doi. 10.1111/j.1365-2516.2012.02849.x
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Peripheral quantitative computed tomography (pQCT) reveals alterations in the three-dimensional bone structure in children with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 955, doi. 10.1111/j.1365-2516.2012.02880.x
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Medical radiation exposure in children with bleeding disorders: an institutional experience.
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- Haemophilia, 2012, v. 18, n. 6, p. 888, doi. 10.1111/j.1365-2516.2012.02851.x
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- Article
Registry of Hemophilia and other bleeding disorders in Syria.
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- Haemophilia, 2012, v. 18, n. 6, p. 851, doi. 10.1111/j.1365-2516.2012.02862.x
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The effect of cooling on coagulation and haemostasis: Should 'Ice' be part of treatment of acute haemarthrosis in haemophilia?
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- Haemophilia, 2012, v. 18, n. 6, p. 843, doi. 10.1111/j.1365-2516.2012.02918.x
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Determinants of participation in patients with severe haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 860, doi. 10.1111/j.1365-2516.2012.02884.x
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- Article
Mutation spectrum and inhibitor risk in 100 Korean patients with severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 6, p. 1008, doi. 10.1111/j.1365-2516.2012.02895.x
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- Article
Experience of recombinant activated factor VII usage during surgery in patients with haemophilia with inhibitors.
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- Haemophilia, 2012, v. 18, n. 6, p. 997, doi. 10.1111/j.1365-2516.2012.02866.x
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- Article
Analysis of F9 point mutations and their correlation to severity of haemophilia B disease.
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- Haemophilia, 2012, v. 18, n. 6, p. 933, doi. 10.1111/j.1365-2516.2012.02848.x
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- Article
Large psoas haematoma and femoral neuropathy in a patient with type 2 B von Willebrand's disease.
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- Haemophilia, 2012, v. 18, n. 6, p. e407, doi. 10.1111/hae.12022
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- Article
Immune system polymorphisms and factor VIII inhibitor formation in Brazilian haemophilia A severe patients.
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- Haemophilia, 2012, v. 18, n. 6, p. e416, doi. 10.1111/hae.12015
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6th Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) 6-8 February 2013, Warsaw, Poland.
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- Haemophilia, 2012, v. 18, n. 6, p. 1014, doi. 10.1111/hae.12037
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- Article
Analyses of recombinant activated factor VII treatments from clinical practice for rapid bleeding and acute pain control in haemophilia patients with inhibitors.
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- Haemophilia, 2012, v. 18, n. 6, p. e409, doi. 10.1111/j.1365-2516.2012.02920.x
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The fraction of recombinant factor VIII:Ag unable to bind von Willebrand factor has no FVIII coagulant activity: studies in vitro.
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- Haemophilia, 2012, v. 18, n. 6, p. 917, doi. 10.1111/j.1365-2516.2012.02861.x
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An MRI scale for assessment of haemophilic arthropathy from the International Prophylaxis Study Group.
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- Haemophilia, 2012, v. 18, n. 6, p. 962, doi. 10.1111/j.1365-2516.2012.02883.x
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Multidisciplinary management of patients with haemophilia with inhibitors undergoing surgery in the United States: perspectives and best practices derived from experienced treatment centres.
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- Haemophilia, 2012, v. 18, n. 6, p. 971, doi. 10.1111/j.1365-2516.2012.02894.x
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Kinetics of the interaction between anti-FVIII antibodies and FVIII from therapeutic concentrates, with and without von Willebrand factor, assessed by surface plasmon resonance.
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- Haemophilia, 2012, v. 18, n. 6, p. 982, doi. 10.1111/j.1365-2516.2012.02858.x
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Feasibility of short message service to document bleeding episodes in children with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 906, doi. 10.1111/j.1365-2516.2012.02869.x
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Spectrum of F8 gene mutations in haemophilia A patients from Slovenia.
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- Haemophilia, 2012, v. 18, n. 6, p. e420, doi. 10.1111/hae.12003
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Corrigendum.
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- 2012
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- Erratum
Trauma-related bleeding complications in South African patients with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. e405, doi. 10.1111/hae.12025
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Joint distraction: a treatment to consider for haemophilic arthropathy.
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- Haemophilia, 2012, v. 18, n. 6, p. e418, doi. 10.1111/hae.12007
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Reply to von Willebrand's disease and postpartum haemorrhage by Chee et al.
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- Haemophilia, 2012, v. 18, n. 6, p. e399, doi. 10.1111/hae.12029
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Regional registry of bleeding disorders in Tunisia.
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- Haemophilia, 2012, v. 18, n. 6, p. e400, doi. 10.1111/j.1365-2516.2012.02930.x
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Factor VIII inhibitors in patients with congenital severe haemophilia A and its relation to genotype.
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- Haemophilia, 2012, v. 18, n. 6, p. e411, doi. 10.1111/j.1365-2516.2012.02923.x
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Polymorphic mi RNA-mediated gene contribution to inhibitor development in haemophilia A.
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- Haemophilia, 2012, v. 18, n. 6, p. 1003, doi. 10.1111/j.1365-2516.2012.02882.x
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Arthroscopic synovectomy of the elbow covered with rFVIIa in a haemophilia B juvenile with inhibitor.
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- Haemophilia, 2012, v. 18, n. 6, p. e414, doi. 10.1111/j.1365-2516.2012.02927.x
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Effect of a self-help program for mothers of hemophilic children in Korea.
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- Haemophilia, 2012, v. 18, n. 6, p. 892, doi. 10.1111/j.1365-2516.2012.02853.x
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Dosing and effectiveness of recombinant activated factor VII (rFVIIA) in congenital haemophilia with inhibitors by bleed type and location: the experience of the Haemophilia and Thrombosis Research Society (HTRS) Registry (2004-2008).
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- Haemophilia, 2012, v. 18, n. 6, p. 990, doi. 10.1111/j.1365-2516.2012.02864.x
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The impact of sport on children with haemophilia.
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- Haemophilia, 2012, v. 18, n. 6, p. 898, doi. 10.1111/j.1365-2516.2012.02857.x
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Pharmacokinetic properties of IB1001, an investigational recombinant factor IX, in patients with haemophilia B: repeat pharmacokinetic evaluation and sialylation analysis.
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- Haemophilia, 2012, v. 18, n. 6, p. 881, doi. 10.1111/j.1365-2516.2012.02897.x
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Daily dosing prophylaxis for haemophilia: a randomized crossover pilot study evaluating feasibility and efficacy.
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- Haemophilia, 2012, v. 18, n. 6, p. 855, doi. 10.1111/j.1365-2516.2012.02879.x
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- Article
Judith Graham Pool and the discovery of cryoprecipitate.
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- Haemophilia, 2012, v. 18, n. 6, p. 833, doi. 10.1111/hae.12042
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A Canadian survey of self-infusion practices in persons with haemophilia A.
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- Haemophilia, 2012, v. 18, n. 6, p. e403, doi. 10.1111/hae.12013
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von Willebrand's disease: a report from a meeting in the Åland islands.
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- Haemophilia, 2012, v. 18, p. 1, doi. 10.1111/j.1365-2516.2012.02925.x
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Acquired, non-amyloid related factor X deficiency: review of the literature.
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- Haemophilia, 2012, v. 18, n. 5, p. 655, doi. 10.1111/j.1365-2516.2012.02773.x
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- Article
Haemophilia prophylaxis: how can we justify the costs?
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- Haemophilia, 2012, v. 18, n. 5, p. 680, doi. 10.1111/j.1365-2516.2012.02790.x
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Platelet inhibition and bleeding complications in patients with haemophilia/von Willebrand's disease and coronary artery disease.
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- Haemophilia, 2012, v. 18, n. 5, p. e364, doi. 10.1111/j.1365-2516.2012.02898.x
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Treatment of Hodgkin's lymphoma in a patient with type III von Willebrand's disease.
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- Haemophilia, 2012, v. 18, n. 5, p. e378, doi. 10.1111/j.1365-2516.2012.02901.x
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A retrospective cohort study of cancer incidence among patients treated with radiosynoviorthesis.
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- Haemophilia, 2012, v. 18, n. 5, p. 805, doi. 10.1111/j.1365-2516.2012.02802.x
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Treatment patterns, health-related quality of life and adherence to prophylaxis among haemophilia A patients in the United States.
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- Haemophilia, 2012, v. 18, n. 5, p. 760, doi. 10.1111/j.1365-2516.2012.02813.x
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F8 gene dosage defects in atypical patients with severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 5, p. 708, doi. 10.1111/j.1365-2516.2012.02818.x
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Is on-demand treatment effective in patients with severe haemophilia?
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- Haemophilia, 2012, v. 18, n. 5, p. 738, doi. 10.1111/j.1365-2516.2012.02806.x
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- Article