Works matching IS 13518216 AND DT 2022 AND VI 28 AND IP 4
Results: 25
Supporting patients with haemophilia in a world of crises: New role for the WFH and its partners.
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- Haemophilia, 2022, v. 28, n. 4, p. 521, doi. 10.1111/hae.14610
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CTLA4‐Ig prevents development of neutralizing antibody formation after continuous treatment with human FVIII in HA rats.
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- Haemophilia, 2022, v. 28, n. 4, p. 568, doi. 10.1111/hae.14573
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Diagnostic evaluation of the first macroscopic haematuria episode in adult haemophilia patients.
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- Haemophilia, 2022, v. 28, n. 4, p. e109, doi. 10.1111/hae.14590
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Eradication of FIX inhibitor in haemophilia B children using low‐dose immune tolerance induction with rituximab‐based immunosuppressive agent(s) in China.
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- Haemophilia, 2022, v. 28, n. 4, p. 625, doi. 10.1111/hae.14577
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Clinical application of extended half‐life factor VIII in children with severe haemophilia A.
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- Haemophilia, 2022, v. 28, n. 4, p. 619, doi. 10.1111/hae.14576
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Does difference between label and actual potency of factor VIII concentrate affect pharmacokinetic‐guided dosing of replacement therapy in haemophilia A?
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- Haemophilia, 2022, v. 28, n. 4, p. 610, doi. 10.1111/hae.14575
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A phase IV, multicentre, open‐label study of emicizumab prophylaxis in people with haemophilia A with or without FVIII inhibitors undergoing minor surgical procedures.
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- Haemophilia, 2022, v. 28, n. 4, p. e105, doi. 10.1111/hae.14574
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Platelet function testing: Current practice among clinical centres in Northern Europe.
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- Haemophilia, 2022, v. 28, n. 4, p. 642, doi. 10.1111/hae.14578
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Examining patient and professional perspectives in the UK for gene therapy in haemophilia.
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- Haemophilia, 2022, v. 28, n. 4, p. 588, doi. 10.1111/hae.14572
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Pain, depression and anxiety in people with haemophilia from three Nordic countries: Cross‐sectional survey data from the MIND study.
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- Haemophilia, 2022, v. 28, n. 4, p. 557, doi. 10.1111/hae.14571
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A review of the pharmacokinetics, efficacy and safety of high‐purity factor X for the prophylactic treatment of hereditary factor X deficiency.
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- Haemophilia, 2022, v. 28, n. 4, p. 523, doi. 10.1111/hae.14570
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ADAMTS‐4 as a possible distinguishing indicator between osteoarthritis and haemophilic arthropathy.
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- Haemophilia, 2022, v. 28, n. 4, p. 656, doi. 10.1111/hae.14569
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Altered brain activity and functional networks in school‐age boys with severe haemophilia A: A resting‐state functional magnetic resonance imaging study.
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- Haemophilia, 2022, v. 28, n. 4, p. 578, doi. 10.1111/hae.14567
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European principles of care for physiotherapy provision for persons with inherited bleeding disorders: Perspectives of physiotherapists and patients.
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- Haemophilia, 2022, v. 28, n. 4, p. 649, doi. 10.1111/hae.14566
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Bone health in haemophilia carriers and persons with von Willebrand disease: A large database analysis.
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- Haemophilia, 2022, v. 28, n. 4, p. 671, doi. 10.1111/hae.14565
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- Article
Most subjectively affected joints in patients with haemophilia – what has changed after 20 years in Germany?
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- Haemophilia, 2022, v. 28, n. 4, p. 663, doi. 10.1111/hae.14564
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Association between weight status and joint function in adult and pediatric patients with hemophilia.
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- Haemophilia, 2022, v. 28, n. 4, p. e101, doi. 10.1111/hae.14541
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Advantages of external quality assessment‐EQA programs.
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- Haemophilia, 2022, v. 28, n. 4, p. 679, doi. 10.1111/hae.14562
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Revised terminal half‐life of nonacog alfa as derived from extended sampling data: A real‐world study involving 64 haemophilia B patients on nonacog alfa regular prophylaxis.
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- Haemophilia, 2022, v. 28, n. 4, p. 542, doi. 10.1111/hae.14560
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Iron deficiency anemia and bleeding management in pediatric patients with Bernard‐Soulier syndrome and Glanzmann Thrombasthenia: A single‐institution analysis.
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- Haemophilia, 2022, v. 28, n. 4, p. 633, doi. 10.1111/hae.14559
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Associated comorbidities, healthcare utilization & mortality in hospitalized patients with haemophilia in the United States: Contemporary nationally representative estimates.
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- Haemophilia, 2022, v. 28, n. 4, p. 532, doi. 10.1111/hae.14557
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Eptacog beta efficacy and safety in the treatment and control of bleeding in paediatric subjects (<12 years) with haemophilia A or B with inhibitors.
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- Haemophilia, 2022, v. 28, n. 4, p. 548, doi. 10.1111/hae.14563
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Anti‐platelet treatment challenges in Glanzmann thrombasthenia‐clinical practice when data lacks.
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- Haemophilia, 2022, v. 28, n. 4, p. e98, doi. 10.1111/hae.14527
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Total joint arthroplasty in the patients with haemophilia: General or neuraxial anaesthesia?
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- Haemophilia, 2022, v. 28, n. 4, p. e95, doi. 10.1111/hae.14509
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Issue Information.
- Published in:
- Haemophilia, 2022, v. 28, n. 4, p. i, doi. 10.1111/hae.14568
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- Article