Works matching IS 13518216 AND DT 2011 AND VI 17 AND IP 4
Results: 30
A case report of a premature infant with haemophilia A and factor VIII inhibitor.
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- Haemophilia, 2011, v. 17, n. 4, p. 711, doi. 10.1111/j.1365-2516.2010.02455.x
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- Article
Use of autologous platelet-rich clots for the prevention of local injury bleeding in patients with severe inherited mucocutaneous bleeding disorders.
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- Haemophilia, 2011, v. 17, n. 4, p. 620, doi. 10.1111/j.1365-2516.2010.02480.x
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- Article
Pharmacoeconomic impact of obesity in severe haemophilia children on clotting factor prophylaxis in a single institution.
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- Haemophilia, 2011, v. 17, n. 4, p. 717, doi. 10.1111/j.1365-2516.2010.02462.x
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- Article
A case-control study reveals immunoregulatory gene haplotypes that influence inhibitor risk in severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 4, p. 641, doi. 10.1111/j.1365-2516.2010.02473.x
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- Article
I need to pay more attention to mild haemophilia patients.
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- Haemophilia, 2011, v. 17, n. 4, p. 704, doi. 10.1111/j.1365-2516.2010.02484.x
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- Article
SEMG activation patterns of thigh muscles during upright standing in haemophilic patients.
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- Haemophilia, 2011, v. 17, n. 4, p. 669, doi. 10.1111/j.1365-2516.2010.02466.x
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- Article
The changing face of hepatitis in boys with haemophilia associated with increased prevalence of obesity.
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- Haemophilia, 2011, v. 17, n. 4, p. 689, doi. 10.1111/j.1365-2516.2010.02477.x
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Comparison of physical activity and sedentary behaviours between young haemophilia A patients and healthy adolescents.
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- Haemophilia, 2011, v. 17, n. 4, p. 676, doi. 10.1111/j.1365-2516.2010.02469.x
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- Article
Pathophysiology, diagnosis and prevention of arthropathy in patients with haemophilia.
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- Haemophilia, 2011, v. 17, n. 4, p. 571, doi. 10.1111/j.1365-2516.2010.02472.x
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- Article
Incomplete tyrosine 1680 sulphation in recombinant FVIII concentrates.
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- Haemophilia, 2011, v. 17, n. 4, p. 709, doi. 10.1111/j.1365-2516.2010.02454.x
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A patient-prioritized ability assessment in haemophilia: the Canadian Occupational Performance Measure.
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- Haemophilia, 2011, v. 17, n. 4, p. 605, doi. 10.1111/j.1365-2516.2010.02465.x
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- Article
Identification of ten large deletions and one duplication in the F8 gene of eleven unrelated Iranian severe haemophilia A families using the multiplex ligation-dependent probe amplification technique.
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- Haemophilia, 2011, v. 17, n. 4, p. 705, doi. 10.1111/j.1365-2516.2010.02476.x
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- Article
Surgery-associated acquired haemophilia and response to combined rituximab and cyclosporine treatment.
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- Haemophilia, 2011, v. 17, n. 4, p. 715, doi. 10.1111/j.1365-2516.2010.02458.x
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Exposure and safety of higher doses of recombinant factor VIIa ≥250 μg kg.
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- Haemophilia, 2011, v. 17, n. 4, p. 650, doi. 10.1111/j.1365-2516.2010.02483.x
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- Article
Surgical Experience with rFVIIa (NovoSeven) in congenital haemophilia A and B patients with inhibitors to factors VIII or IX.
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- Haemophilia, 2011, v. 17, n. 4, p. 579, doi. 10.1111/j.1365-2516.2010.02460.x
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- Article
Long-term follow-up of prophylaxis with recombinant activated factor VII in patients with congenital factor VII deficiency.
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- Haemophilia, 2011, v. 17, n. 4, p. 713, doi. 10.1111/j.1365-2516.2010.02471.x
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- Article
An aberrant pattern for intron 1 inversion of factor VIII gene.
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- Haemophilia, 2011, v. 17, n. 4, p. 708, doi. 10.1111/j.1365-2516.2010.02482.x
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- Article
Recombinant factor concentrates may increase inhibitor development: a single centre cohort study.
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- Haemophilia, 2011, v. 17, n. 4, p. 625, doi. 10.1111/j.1365-2516.2010.02464.x
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- Article
Assessment of musculoskeletal function and mood in haemophilia A adolescents: a cross-sectional study.
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- Haemophilia, 2011, v. 17, n. 4, p. 683, doi. 10.1111/j.1365-2516.2010.02475.x
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- Article
A rare case of an acquired inhibitor to factor IX.
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- Haemophilia, 2011, v. 17, n. 4, p. 712, doi. 10.1111/j.1365-2516.2010.02457.x
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- Article
Alloantibodies to factor VIII in haemophilia.
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- Haemophilia, 2011, v. 17, n. 4, p. 636, doi. 10.1111/j.1365-2516.2010.02468.x
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Bone turnover markers and bone mineral density in children with haemophilia.
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- Haemophilia, 2011, v. 17, n. 4, p. 657, doi. 10.1111/j.1365-2516.2010.02439.x
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Assessment of acute and persistent pain management in patients with haemophilia.
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- Haemophilia, 2011, v. 17, n. 4, p. 612, doi. 10.1111/j.1365-2516.2010.02479.x
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A clinical study assessing the pharmacokinetics, efficacy and safety of AlphaNine.
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- Haemophilia, 2011, v. 17, n. 4, p. 590, doi. 10.1111/j.1365-2516.2010.02470.x
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International comparative field study of N8 evaluating factor VIII assay performance.
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- Haemophilia, 2011, v. 17, n. 4, p. 695, doi. 10.1111/j.1365-2516.2010.02481.x
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- Article
Prevalence and risk factors of cardiovascular disease (CVD) events among patients with haemophilia: experience of a single haemophilia treatment centre in the United States (US).
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- Haemophilia, 2011, v. 17, n. 4, p. 597, doi. 10.1111/j.1365-2516.2010.02463.x
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The Swedish version of the Haemophilia Activity List.
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- Haemophilia, 2011, v. 17, n. 4, p. 662, doi. 10.1111/j.1365-2516.2010.02474.x
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Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products.
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- Haemophilia, 2011, v. 17, n. 4, p. 703, doi. 10.1111/j.1365-2516.2010.02485.x
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- Article
An improved, semi quantitative clot based assay for factor XIII.
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- Haemophilia, 2011, v. 17, n. 4, p. 718, doi. 10.1111/j.1365-2516.2010.02456.x
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Sequential combined bypassing therapy is safe and effective in the treatment of unresponsive bleeding in adults and children with haemophilia and inhibitors.
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- Haemophilia, 2011, v. 17, n. 4, p. 630, doi. 10.1111/j.1365-2516.2010.02467.x
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- Article