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Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008.
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- Haemophilia, 2012, v. 18, n. 2, p. 268, doi. 10.1111/j.1365-2516.2011.02692.x
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- Article
Haemostasis prophylaxis using single dose desmopressin acetate and extended use epsilon aminocaproic acid for adenotonsillectomy in patients with type 1 von Willebrand disease.
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- Haemophilia, 2012, v. 18, n. 2, p. 200, doi. 10.1111/j.1365-2516.2011.02619.x
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Health care expenditures for Medicaid-covered males with haemophilia in the United States, 2008.
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- Haemophilia, 2012, v. 18, n. 2, p. 276, doi. 10.1111/j.1365-2516.2011.02713.x
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Heterozygote frequencies of common polymorphic markers of factor VIII ( f8) and factor IX ( f9) genes in indigenous Nepali population.
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- Haemophilia, 2012, v. 18, n. 2, p. e44, doi. 10.1111/j.1365-2516.2011.02736.x
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Activated factor VII: my story.
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- Haemophilia, 2012, v. 18, n. 2, p. 147, doi. 10.1111/j.1365-2516.2012.02753.x
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The status of carrier and prenatal diagnosis of haemophilia in China.
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- Haemophilia, 2012, v. 18, n. 2, p. 235, doi. 10.1111/j.1365-2516.2011.02630.x
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Factor VIII haplotypes of Japanese population show similarity to those of Caucasian populations.
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- Haemophilia, 2012, v. 18, n. 2, p. e43, doi. 10.1111/j.1365-2516.2011.02715.x
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On-demand treatment of bleeds in haemophilia patients with inhibitors: strategies for securing and maintaining predictable efficacy with recombinant activated factor VII.
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- Haemophilia, 2012, v. 18, n. 2, p. 255, doi. 10.1111/j.1365-2516.2011.02612.x
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Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
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- Haemophilia, 2012, v. 18, n. 2, p. 205, doi. 10.1111/j.1365-2516.2011.02621.x
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The economics of inpatient on-demand treatment for haemophilia with high-responding inhibitors: a US retrospective data analysis.
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- Haemophilia, 2012, v. 18, n. 2, p. 284, doi. 10.1111/j.1365-2516.2011.02623.x
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Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius.
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- Haemophilia, 2012, v. 18, n. 2, p. 222, doi. 10.1111/j.1365-2516.2011.02616.x
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Another role for the VW molecule.
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- Haemophilia, 2012, v. 18, n. 2, p. 246, doi. 10.1111/j.1365-2516.2011.02696.x
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Benefits associated with a broad selection of dosage strengths for recombinant factor VIII products.
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- Haemophilia, 2012, v. 18, n. 2, p. 182, doi. 10.1111/j.1365-2516.2011.02627.x
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The influence of prophylactic factor VIII in severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 2, p. 193, doi. 10.1111/j.1365-2516.2011.02638.x
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Health technology assessment and haemophilia.
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- Haemophilia, 2012, v. 18, n. 2, p. 152, doi. 10.1111/j.1365-2516.2012.02754.x
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Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes.
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- Haemophilia, 2012, v. 18, n. 2, p. e55, doi. 10.1111/j.1365-2516.2011.02707.x
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Immunoprotective effect of von Willebrand factor towards therapeutic factor VIII in experimental haemophilia A.
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- Haemophilia, 2012, v. 18, n. 2, p. 248, doi. 10.1111/j.1365-2516.2011.02679.x
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Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency.
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- Haemophilia, 2012, v. 18, n. 2, p. e51, doi. 10.1111/j.1365-2516.2011.02747.x
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First trimester sonographic determination of foetal gender: a cost effective non-invasive technique for prenatal screening of haemophilia in low income countries.
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- Haemophilia, 2012, v. 18, n. 2, p. e49, doi. 10.1111/j.1365-2516.2011.02729.x
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A severe haemophiliac patient with acute coronary syndrome admitted to cardiac rehabilitation.
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- Haemophilia, 2012, v. 18, n. 2, p. e45, doi. 10.1111/j.1365-2516.2011.02746.x
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Platelet factor V levels in moderate to severe congenital factor V deficiency.
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- Haemophilia, 2012, v. 18, n. 2, p. e53, doi. 10.1111/j.1365-2516.2011.02717.x
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Molecular evidence of HIV-1 transmission in 20 Korean individuals with haemophilia: phylogenetic analysis of the vif gene.
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- Haemophilia, 2012, v. 18, n. 2, p. 291, doi. 10.1111/j.1365-2516.2011.02620.x
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Cord blood hematopoietic stem cell transplantation in an adolescent with haemophilia.
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- Haemophilia, 2012, v. 18, n. 2, p. e48, doi. 10.1111/j.1365-2516.2011.02734.x
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Effect of intracranial bleeds on the neurocognitive, academic, behavioural and adaptive functioning of boys with haemophilia.
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- Haemophilia, 2012, v. 18, n. 2, p. 229, doi. 10.1111/j.1365-2516.2011.02632.x
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Changes in the levels of factor VIII and von Willebrand factor in the puerperium.
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- Haemophilia, 2012, v. 18, n. 2, p. 241, doi. 10.1111/j.1365-2516.2011.02625.x
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Treatment of haemophilia A and B and von Willebrand's disease: summary and conclusions of a systematic review as part of a Swedish health-technology assessment.
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- Haemophilia, 2012, v. 18, n. 2, p. 158, doi. 10.1111/j.1365-2516.2011.02723.x
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Retrospective analysis of differences in annual factor VIII utilization among haemophilia A patients.
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- Haemophilia, 2012, v. 18, n. 2, p. 187, doi. 10.1111/j.1365-2516.2011.02636.x
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Risk of inhibitor development in mild haemophilia A increases with age.
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- Haemophilia, 2012, v. 18, n. 2, p. 263, doi. 10.1111/j.1365-2516.2011.02629.x
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Clinical efficacy, safety and pharmacokinetic properties of the plasma-derived factor IX concentrate Haemonine<sup>®</sup> in previously treated patients with severe haemophilia B.
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- Haemophilia, 2012, v. 18, n. 2, p. 175, doi. 10.1111/j.1365-2516.2011.02624.x
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Liver transplantation in the haemophilia patient.
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- Haemophilia, 2012, v. 18, n. 2, p. 300, doi. 10.1111/j.1365-2516.2011.02631.x
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Exploring internet needs and use among adolescents with haemophilia: a website development project.
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- Haemophilia, 2012, v. 18, n. 2, p. 216, doi. 10.1111/j.1365-2516.2011.02613.x
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Prolonged bleeding after exfoliation of a deciduous tooth in a patient with Glanzmann's thrombasthenia.
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- Haemophilia, 2012, v. 18, n. 2, p. e58, doi. 10.1111/j.1365-2516.2011.02727.x
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Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran.
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- Haemophilia, 2012, v. 18, n. 2, p. 211, doi. 10.1111/j.1365-2516.2011.02635.x
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The natural history of mild haemophilia: a 30-year single centre experience.
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- Haemophilia, 2012, v. 18, n. 2, p. 166, doi. 10.1111/j.1365-2516.2011.02617.x
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