Found: 80
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Porcine factor VIII.
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- Haemophilia, 2012, v. 18, n. 3, p. 305, doi. 10.1111/j.1365-2516.2012.02803.x
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- Article
Exploring the biological basis of haemophilic joint disease: experimental studies.
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- Haemophilia, 2012, v. 18, n. 3, p. 310, doi. 10.1111/j.1365-2516.2011.02669.x
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Recommendations for assessment, monitoring and follow-up of patients with haemophilia.
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- Haemophilia, 2012, v. 18, n. 3, p. 319, doi. 10.1111/j.1365-2516.2011.02671.x
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Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case-control survey study.
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- Haemophilia, 2012, v. 18, n. 3, p. 326, doi. 10.1111/j.1365-2516.2011.02626.x
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Healthcare resource utilization among haemophilia A patients in the United States.
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- Haemophilia, 2012, v. 18, n. 3, p. 332, doi. 10.1111/j.1365-2516.2011.02677.x
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Deaths associated with acquired haemophilia in France from 2000 to 2009: multiple cause analysis for best care strategies.
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- Haemophilia, 2012, v. 18, n. 3, p. 339, doi. 10.1111/j.1365-2516.2011.02647.x
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Health-related quality of life and psychological well-being in elderly patients with haemophilia.
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- Haemophilia, 2012, v. 18, n. 3, p. 345, doi. 10.1111/j.1365-2516.2011.02643.x
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Cross-cultural validation of the CHO-KLAT and HAEMO-QoL-A in Canadian French.
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- Haemophilia, 2012, v. 18, n. 3, p. 353, doi. 10.1111/j.1365-2516.2011.02703.x
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- Article
Pre-operative flexion contracture determines the functional outcome of haemophilic arthropathy treated with total knee arthroplasty.
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- Haemophilia, 2012, v. 18, n. 3, p. 358, doi. 10.1111/j.1365-2516.2011.02695.x
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Ultrasonography of haemophilic arthropathy.
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- Haemophilia, 2012, v. 18, n. 3, p. 364, doi. 10.1111/j.1365-2516.2011.02672.x
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Identification and long-term observation of early joint damage by magnetic resonance imaging in clinically asymptomatic joints in patients with haemophilia A or B despite prophylaxis.
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- Haemophilia, 2012, v. 18, n. 3, p. 369, doi. 10.1111/j.1365-2516.2011.02682.x
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F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity.
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- Haemophilia, 2012, v. 18, n. 3, p. 375, doi. 10.1111/j.1365-2516.2011.02700.x
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Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey.
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- Haemophilia, 2012, v. 18, n. 3, p. 383, doi. 10.1111/j.1365-2516.2011.02693.x
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Patient/Caregiver-reported recombinant factor VIIa (rFVIIa) dosing: home treatment of acute bleeds in the Dosing Observational Study in Hemophilia (DOSE).
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- Haemophilia, 2012, v. 18, n. 3, p. 392, doi. 10.1111/j.1365-2516.2011.02704.x
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U.S. survey of surgical capabilities and experience with surgical procedures in patients with congenital haemophilia with inhibitors.
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- Haemophilia, 2012, v. 18, n. 3, p. 400, doi. 10.1111/j.1365-2516.2011.02698.x
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- Article
Pregnancy in type 2B VWD: a case series.
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- Haemophilia, 2012, v. 18, n. 3, p. 406, doi. 10.1111/j.1365-2516.2011.02691.x
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The outcome of endometrial ablation in women with inherited bleeding disorders.
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- Haemophilia, 2012, v. 18, n. 3, p. 413, doi. 10.1111/j.1365-2516.2011.02712.x
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Operative management and outcomes in children with congenital bleeding disorders: a retrospective review at a single haemophilia treatment centre.
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- Haemophilia, 2012, v. 18, n. 3, p. 421, doi. 10.1111/j.1365-2516.2011.02667.x
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Circumcision and complications in patients with haemophilia in southern part of Turkey: Çukurova experience.
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- Haemophilia, 2012, v. 18, n. 3, p. 426, doi. 10.1111/j.1365-2516.2011.02706.x
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Pharmacokinetic properties of two different recombinant activated factor VII formulations.
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- Haemophilia, 2012, v. 18, n. 3, p. 431, doi. 10.1111/j.1365-2516.2011.02674.x
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Severe haemophilia A patients have reduced numbers of peripheral memory B cells.
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- Haemophilia, 2012, v. 18, n. 3, p. 437, doi. 10.1111/j.1365-2516.2011.02642.x
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Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease.
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- Haemophilia, 2012, v. 18, n. 3, p. 444, doi. 10.1111/j.1365-2516.2011.02645.x
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A Modified I-PCR to detect the factor VIII Inv22 for genetic diagnosis and prenatal diagnosis in haemophilia A.
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- Haemophilia, 2012, v. 18, n. 3, p. 452, doi. 10.1111/j.1365-2516.2011.02670.x
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Protein C, protein S and von Willebrand factor levels correlate with bleeding symptoms: a population-based study.
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- Haemophilia, 2012, v. 18, n. 3, p. 457, doi. 10.1111/j.1365-2516.2011.02678.x
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Whole blood rotation thromboelastometry (ROTEM<sup>®</sup>) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V.
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- Haemophilia, 2012, v. 18, n. 3, p. 463, doi. 10.1111/j.1365-2516.2011.02710.x
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Understanding FVIII/VWF complex - report from a symposium of XXIX WFH meeting 2010.
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- Haemophilia, 2012, v. 18, n. 3, p. 469, doi. 10.1111/j.1365-2516.2011.02655.x
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Abstracts of articles published in the May 2012 online supplement.
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- Haemophilia, 2012, v. 18, n. 3, p. 476, doi. 10.1111/j.1365-2516.2012.02788.x
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- Article
The international factor IX treatment network survey.
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- Haemophilia, 2012, v. 18, n. 3, p. e60, doi. 10.1111/j.1365-2516.2012.02767.x
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Invasive procedures and minor surgery in factor VII deficiency.
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- Haemophilia, 2012, v. 18, n. 3, p. e63, doi. 10.1111/j.1365-2516.2012.02751.x
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The challenging management of a child with type 3 von Willebrand disease and antibodies to von Willebrand factor.
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- Haemophilia, 2012, v. 18, n. 3, p. e66, doi. 10.1111/j.1365-2516.2012.02799.x
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Successful immune tolerance induction in two boys with haemophilia B and inhibitory antibodies.
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- Haemophilia, 2012, v. 18, n. 3, p. e67, doi. 10.1111/j.1365-2516.2012.02784.x
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Re-emergence of a low-titre factor VIII inhibitor after liver transplant.
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- Haemophilia, 2012, v. 18, n. 3, p. e69, doi. 10.1111/j.1365-2516.2012.02811.x
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A study of 46 patients with acquired haemophilia A in Taiwan finds elevated LDH level and mucosal bleedings associated with reduced response to immunosuppressive therapy.
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- Haemophilia, 2012, v. 18, n. 3, p. e71, doi. 10.1111/j.1365-2516.2012.02807.x
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Acquired haemophilia in a patient treated with interferon-α for hepatitis C infection.
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- Haemophilia, 2012, v. 18, n. 3, p. e73, doi. 10.1111/j.1365-2516.2012.02775.x
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Acquired haemophilia A treated with Rituximab in a patient with prostatic melioidosis.
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- Haemophilia, 2012, v. 18, n. 3, p. e74, doi. 10.1111/j.1365-2516.2012.02800.x
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Complete immunotolerance induction after FEIBA prophylaxis in a haemophilia A patient with high-titre inhibitor.
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- Haemophilia, 2012, v. 18, n. 3, p. e75, doi. 10.1111/j.1365-2516.2012.02776.x
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Aphthous oral ulceration and its successful management by Lactobacillus brevis CD2 extract in an adult haemophilic patient.
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- Haemophilia, 2012, v. 18, n. 3, p. e78, doi. 10.1111/j.1365-2516.2012.02757.x
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von Willebrand factor: demographics of plasma protein level in a large blood donor cohort from South Wales in the United Kingdom.
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- Haemophilia, 2012, v. 18, n. 3, p. e79, doi. 10.1111/j.1365-2516.2012.02782.x
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Pain management issues in haemophilia.
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- Haemophilia, 2012, v. 18, n. 3, p. e81, doi. 10.1111/j.1365-2516.2012.02764.x
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Does weight reduction in haemophilia lead to a decrease in joint bleeds?
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- Haemophilia, 2012, v. 18, n. 3, p. e82, doi. 10.1111/j.1365-2516.2011.02521.x
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Non-operative management of blunt major hepatic injury in a young adult with severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 3, p. e84, doi. 10.1111/j.1365-2516.2012.02761.x
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Acquired factor V deficiency and mini literature review.
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- Haemophilia, 2012, v. 18, n. 3, p. e86, doi. 10.1111/j.1365-2516.2011.02650.x
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How we manage prostate biopsy and prostate cancer therapy in men with haemophilia.
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- Haemophilia, 2012, v. 18, n. 3, p. e88, doi. 10.1111/j.1365-2516.2012.02787.x
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A study of variations in the reported haemophilia B prevalence around the world.
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- Haemophilia, 2012, v. 18, n. 3, p. e91, doi. 10.1111/j.1365-2516.2011.02588.x
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- Article
Utilization patterns and associated costs of factor assistance programmes among persons with haemophilia: a single institution review.
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- Haemophilia, 2012, v. 18, n. 3, p. e95, doi. 10.1111/j.1365-2516.2011.02649.x
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Psychosocial aspects of haemophilia: a systematic review of methodologies and findings.
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- Haemophilia, 2012, v. 18, n. 3, p. e101, doi. 10.1111/j.1365-2516.2011.02683.x
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A national study of pain in the bleeding disorders community: a description of haemophilia pain.
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- Haemophilia, 2012, v. 18, n. 3, p. e115, doi. 10.1111/j.1365-2516.2011.02709.x
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A qualitative study identifying the knowledge, attitudes and behaviours of young men with mild haemophilia.
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- Haemophilia, 2012, v. 18, n. 3, p. e120, doi. 10.1111/j.1365-2516.2011.02714.x
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Emergency and out of hours care of patients with inherited bleeding disorders.
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- Haemophilia, 2012, v. 18, n. 3, p. e126, doi. 10.1111/j.1365-2516.2011.02721.x
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Investigation of disease-associated factors in haemophilia A patients without detectable mutations.
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- Haemophilia, 2012, v. 18, n. 3, p. e132, doi. 10.1111/j.1365-2516.2011.02737.x
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- Article