Works matching IS 13518216 AND DT 2012 AND VI 18 AND IP 5
Results: 46
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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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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Malignant disease in the haemophilic population: moving towards a management consensus?
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- Haemophilia, 2012, v. 18, n. 5, p. 664, doi. 10.1111/j.1365-2516.2012.02846.x
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Acquired haemophilia A. First line treatment with calcineurin inhibitors and steroid pulses: a 10-year follow-up study.
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- Haemophilia, 2012, v. 18, n. 5, p. 789, doi. 10.1111/j.1365-2516.2012.02772.x
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The group medical appointment (GMA) in haemophilia and von Willebrand's disease: a new development in outpatient paediatric care.
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- Haemophilia, 2012, v. 18, n. 5, p. 766, doi. 10.1111/j.1365-2516.2012.02783.x
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The AIDS epidemic in haemophilia patients II: pursuing absolute viral safety of clotting factor concentrates 1985-1988.
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- Haemophilia, 2012, v. 18, n. 5, p. 649, doi. 10.1111/hae.12000
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The importance of haemophilia treatment centre administrators in patient care.
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- Haemophilia, 2012, v. 18, n. 5, p. e366, doi. 10.1111/j.1365-2516.2012.02900.x
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Efficacy evaluation of products for treatment of bleeding episodes.
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- Haemophilia, 2012, v. 18, n. 5, p. e367, doi. 10.1111/j.1365-2516.2012.02911.x
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Late immune tolerance induction in an adult with severe haemophilia A and high-responder inhibitor: 1-year outcome.
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- Haemophilia, 2012, v. 18, n. 5, p. e388, doi. 10.1111/j.1365-2516.2012.02870.x
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Is it justifiable to transplant infected livers into haemophilia recipients?
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- Haemophilia, 2012, v. 18, n. 5, p. 685, doi. 10.1111/j.1365-2516.2012.02801.x
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Characterization of tyrosine sulphation in rFVIII (turoctocog alfa) expressed in CHO and HEK-293 cells.
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- Haemophilia, 2012, v. 18, n. 5, p. e397, doi. 10.1111/j.1365-2516.2012.02881.x
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Joint distraction results in clinical and structural improvement of haemophilic ankle arthropathy: a series of three cases.
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- Haemophilia, 2012, v. 18, n. 5, p. 810, doi. 10.1111/j.1365-2516.2012.02805.x
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Efficacy of factor IX Grifols<sup>®</sup> in surgery: experience of an international multicentre retrospective study.
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- Haemophilia, 2012, v. 18, n. 5, p. e372, doi. 10.1111/j.1365-2516.2012.02919.x
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Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients.
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- Haemophilia, 2012, v. 18, n. 5, p. 794, doi. 10.1111/j.1365-2516.2012.02845.x
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Cartilage restoration in haemophilia: advanced therapies.
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- Haemophilia, 2012, v. 18, n. 5, p. 672, doi. 10.1111/j.1365-2516.2012.02816.x
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Treatment of spontaneous intracerebral haemorrhage in Glanzmann's thrombasthenia.
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- Haemophilia, 2012, v. 18, n. 5, p. e381, doi. 10.1111/j.1365-2516.2012.02878.x
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The potential role of synovial thrombomodulin in the pathophysiology of joint bleeds in haemophilia.
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- Haemophilia, 2012, v. 18, n. 5, p. 818, doi. 10.1111/j.1365-2516.2012.02809.x
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E-learning improves knowledge and practical skills in haemophilia patients on home treatment: a randomized controlled trial.
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- Haemophilia, 2012, v. 18, n. 5, p. 693, doi. 10.1111/j.1365-2516.2012.02786.x
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Methodological concerns regarding 'Assessment of von Willebrand disease as a risk factor for primary postpartum haemorrhage'.
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- Haemophilia, 2012, v. 18, n. 5, p. e379, doi. 10.1111/j.1365-2516.2012.02910.x
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Rare coagulation disorders: a study of 70 cases in the Egyptian population.
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- Haemophilia, 2012, v. 18, n. 5, p. e386, doi. 10.1111/j.1365-2516.2012.02914.x
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Evaluation of the safety and efficacy of recombinant factor IX (nonacog alfa) in minimally treated and previously treated Chinese patients with haemophilia B.
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- Haemophilia, 2012, v. 18, n. 5, p. e374, doi. 10.1111/j.1365-2516.2012.02907.x
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Successful in vitro fertilization and pregnancy in Glanzmann thrombasthenia.
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- Haemophilia, 2012, v. 18, n. 5, p. e380, doi. 10.1111/j.1365-2516.2012.02873.x
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False-positive results in ELISA-based anti FVIII antibody assay may occur with lupus anticoagulant and phospholipid antibodies.
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- Haemophilia, 2012, v. 18, n. 5, p. 777, doi. 10.1111/j.1365-2516.2012.02781.x
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Intrafamilial transmission of hepatitis C virus in patients with severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 5, p. 824, doi. 10.1111/j.1365-2516.2012.02792.x
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Surgical treatment of a complete symptomatic ossification of quadratus femoris muscle in a young haemophilic patient.
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- Haemophilia, 2012, v. 18, n. 5, p. e395, doi. 10.1111/j.1365-2516.2012.02877.x
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Pain management in patients with haemophilia: a European survey.
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- Haemophilia, 2012, v. 18, n. 5, p. 743, doi. 10.1111/j.1365-2516.2012.02808.x
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Mortality, health care utilization and associated diagnoses in hospitalized patients with haemophilia in the United States: first reported nationwide estimates.
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- Haemophilia, 2012, v. 18, n. 5, p. 688, doi. 10.1111/j.1365-2516.2012.02774.x
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The impact of a specific aqua-training for adult haemophilic patients - results of the WATERCISE study (WAT-QoL).
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- Haemophilia, 2012, v. 18, n. 5, p. 714, doi. 10.1111/j.1365-2516.2012.02819.x
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Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran.
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- Haemophilia, 2012, v. 18, n. 5, p. 773, doi. 10.1111/j.1365-2516.2012.02785.x
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Pharmacokinetics and safety of OBI-1, a recombinant B domain-deleted porcine factor VIII, in subjects with haemophilia A.
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- Haemophilia, 2012, v. 18, n. 5, p. 798, doi. 10.1111/j.1365-2516.2012.02789.x
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Severe factor V deficiency in two brothers with different clinical presentations.
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- Haemophilia, 2012, v. 18, n. 5, p. e383, doi. 10.1111/j.1365-2516.2012.02902.x
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Abdominal pain in a patient with haemophilia and metallic valve replacement.
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- Haemophilia, 2012, v. 18, n. 5, p. e370, doi. 10.1111/j.1365-2516.2012.02913.x
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Continuous infusion in haemophilia: current practice in Europe.
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- Haemophilia, 2012, v. 18, n. 5, p. 753, doi. 10.1111/j.1365-2516.2012.02810.x
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Late-Breaking Abstracts from the WFH 2012 Hemophilia World Congress.
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- Haemophilia, 2012, v. 18, n. 5, p. 828, doi. 10.1111/j.1365-2516.2012.02924.x
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Allergenic vaccines administration and inhibitor development in haemophilia.
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- Haemophilia, 2012, v. 18, n. 5, p. e392, doi. 10.1111/j.1365-2516.2012.02872.x
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Successful treatment of acquired haemophilia in a patient with bullous pemphigoid with single-dosing regimen of rituximab.
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- Haemophilia, 2012, v. 18, n. 5, p. e393, doi. 10.1111/j.1365-2516.2012.02917.x
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Tertiary prophylaxis in adults: is there a rationale?
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- Haemophilia, 2012, v. 18, n. 5, p. 722, doi. 10.1111/j.1365-2516.2012.02843.x
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A sensitive venous bleeding model in haemophilia A mice: effects of two recombinant FVIII products (N8 and Advate<sup>®</sup>).
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- Haemophilia, 2012, v. 18, n. 5, p. 782, doi. 10.1111/j.1365-2516.2012.02780.x
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Quality of life in haemophilia A: Hemophilia Utilization Group Study Va (HUGS-Va).
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- Haemophilia, 2012, v. 18, n. 5, p. 699, doi. 10.1111/j.1365-2516.2012.02791.x
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Haemophilia Care in Europe: the ESCHQoL study.
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- Haemophilia, 2012, v. 18, n. 5, p. 729, doi. 10.1111/j.1365-2516.2012.02847.x
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