Works matching IS 13518216 AND DT 2017 AND VI 23 AND IP 1
Results: 31
The demographics, treatment characteristics and quality of life of adult people with haemophilia in China - results from the HERO study.
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- Haemophilia, 2017, v. 23, n. 1, p. 89, doi. 10.1111/hae.13071
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Physician trust and depression influence adherence to factor replacement: a single-centre cross-sectional study.
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- Haemophilia, 2017, v. 23, n. 1, p. 98, doi. 10.1111/hae.13078
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Clinical characteristics of two patients with α1-antitrypsin Pittsburgh in a Chinese family.
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- Haemophilia, 2017, v. 23, n. 1, p. e33, doi. 10.1111/hae.13113
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Low-factor consumption for major surgery in haemophilia B with long-acting recombinant glyco PEGylated factor IX.
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- Haemophilia, 2017, v. 23, n. 1, p. 67, doi. 10.1111/hae.13041
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Trunk muscle activation characteristics in patients with severe haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. 122, doi. 10.1111/hae.13037
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Treatment of acute bleeding in acquired haemophilia A with recombinant activated factor VII: analysis of 10-year Japanese postmarketing surveillance data.
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- Haemophilia, 2017, v. 23, n. 1, p. 50, doi. 10.1111/hae.13033
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The impact of a haemophilia education intervention on the knowledge and health related quality of life of parents of Indian children with haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. 82, doi. 10.1111/hae.13070
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Recombinant porcine sequence factor VIII (rp FVIII) for acquired haemophilia A: practical clinical experience of its use in seven patients.
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- Haemophilia, 2017, v. 23, n. 1, p. 25, doi. 10.1111/hae.13040
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Long-term outcome of total hip arthroplasty in patients with haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. 129, doi. 10.1111/hae.13045
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Low dose prophylaxis in Tunisian children with haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. 77, doi. 10.1111/hae.13048
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A phase III clinical trial of a mixture agent of plasma-derived factor VIIa and factor X ( MC710) in haemophilia patients with inhibitors.
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- Haemophilia, 2017, v. 23, n. 1, p. 59, doi. 10.1111/hae.13050
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Efficacy and safety of point-of-care ultrasound-guided intra-articular corticosteroid joint injections in patients with haemophilic arthropathy.
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- Haemophilia, 2017, v. 23, n. 1, p. 135, doi. 10.1111/hae.13057
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Relative contributions of bleeding scores and iron status on health-related quality of life in von Willebrand disease: a cross-sectional study.
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- Haemophilia, 2017, v. 23, n. 1, p. 115, doi. 10.1111/hae.13062
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Prevalence and predictors of loss to follow-up in young adults with mild haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. e36, doi. 10.1111/hae.13114
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RCT - subjective physical performance and quality of life after a 6-month programmed sports therapy (PST) in patients with haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. 144, doi. 10.1111/hae.13079
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Visualization of haemophilic arthropathy in F8<sup>−/−</sup> rats by ultrasonography and micro-computed tomography.
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- Haemophilia, 2017, v. 23, n. 1, p. 152, doi. 10.1111/hae.13080
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Choosing outcome assessment tools in haemophilia care and research: a multidisciplinary perspective.
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- Haemophilia, 2017, v. 23, n. 1, p. 11, doi. 10.1111/hae.13088
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Pilot study on <sup>18</sup>F-FDG PET/CT for detection of inflammatory changes in blood-induced knee arthropathy in a rabbit model.
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- Haemophilia, 2017, v. 23, n. 1, p. e25, doi. 10.1111/hae.13090
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Instructions to Authors.
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- Haemophilia, 2017, v. 23, n. 1, p. 164, doi. 10.1111/hae.13092
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- Article
Issue Information.
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- Haemophilia, 2017, v. 23, n. 1, p. 1, doi. 10.1111/hae.13093
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- Article
The importance of mRNA structure in determining the pathogenicity of synonymous and non-synonymous mutations in haemophilia.
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- Haemophilia, 2017, v. 23, n. 1, p. e8, doi. 10.1111/hae.13107
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Recombinant B-domain-deleted porcine sequence factor VIII (r- pFVIII) for the treatment of bleeding in patients with congenital haemophilia A and inhibitors.
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- Haemophilia, 2017, v. 23, n. 1, p. 33, doi. 10.1111/hae.13108
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European retrospective study of real-life haemophilia treatment.
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- Haemophilia, 2017, v. 23, n. 1, p. 105, doi. 10.1111/hae.13111
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Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein ( rFVIIIFc) in the A-LONG and Kids A- LONG Studies.
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- Haemophilia, 2017, v. 23, n. 1, p. e39, doi. 10.1111/hae.13125
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Measuring the quality of haemophilia care across different settings: a set of performance indicators derived from demographics data.
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- Haemophilia, 2017, v. 23, n. 1, p. e1, doi. 10.1111/hae.13127
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Balance evaluation in haemophilic preadolescent patients using Nintendo Wii Balance Board<sup>®</sup>.
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- Haemophilia, 2017, v. 23, n. 1, p. e18, doi. 10.1111/hae.13128
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Determining the health-related quality of life in individuals with haemophilia in developing economies: results from the Brazilian population.
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- Haemophilia, 2017, v. 23, n. 1, p. 42, doi. 10.1111/hae.13130
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Pilot randomized, non-inferiority, cross-over trial of once-weekly vs. three times-weekly recombinant factor VIII prophylaxis in adults with severe haemophilia A.
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- Haemophilia, 2017, v. 23, n. 1, p. e43, doi. 10.1111/hae.13131
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Possible assessment of coagulation function and haemostasis therapy using comprehensive coagulation assays in a patient with acquired haemophilia A.
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- Haemophilia, 2017, v. 23, n. 1, p. e46, doi. 10.1111/hae.13134
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Experience of tailoring prophylaxis using factor VIII pharmacokinetic parameters estimated with myPKFiT<sup>®</sup> in patients with severe haemophilia A without inhibitors.
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- Haemophilia, 2017, v. 23, n. 1, p. e50, doi. 10.1111/hae.13141
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Rapid identification of the intron 22 inversion in haemophilia A.
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- Haemophilia, 2017, v. 23, n. 1, p. e55, doi. 10.1111/hae.13142
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