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期刊名:Haemophilia

缩写:HAEMOPHILIA

ISSN:1351-8216

e-ISSN:1365-2516

IF/分区:3.0/Q2

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共收录本刊相关文章索引4435
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Carla Daffunchio,Gustavo Galatro,Martín Rossi et al. Carla Daffunchio et al.
Introduction: Primary prophylaxis is the current gold standard in haemophilia care for the prevention of bleeding and ensuing joint damage. Early detection of joint bleeding, whether symptomatic or subclinical, preferably...
Jan Astermark,Anna Olsson,Pierre Chelle et al. Jan Astermark et al.
Introduction: The use of pharmacokinetic assessment for optimal prophylactic dosing of factor concentrates in haemophilia has gained increasing enthusiasm over the last decade. However, blood sampling on several occasions...
Johanna Wilhelmina Hoefnagels,Kathelijn Fischer,Ruud A T Bos et al. Johanna Wilhelmina Hoefnagels et al.
Introduction: Adherence to prophylactic treatment (prophylaxis) in persons with haemophilia is challenging and has been reported at only ±50%. Acceptance problems are one of the main reasons for non-adherence in haemophi...
Johnny Mahlangu,Howard Levy,Martin Lee et al. Johnny Mahlangu et al.
Aim: Phase 2b study to assess efficacy, safety, thrombogenicity, immunogenicity and tolerability with 28 days of daily dosing of subcutaneous (SQ) dalcinonacog alfa as prophylaxis for haemophilia B (HB). ...
Pier Mannuccio Mannucci,Paolo Angelo Cortesi,Matteo Nicola Dario Di Minno et al. Pier Mannuccio Mannucci et al.
The need to reduce the burden of injections, and improve adherence and clinical outcomes in haemophilia A led to the development of recombinant FVIII products endowed with an extended plasma half-life (EHL-rFVIII) in comparison with standar...
Marcel A L Hendriks,Johanna W M van Wanroij,Britta A P Laros-van Gorkom et al. Marcel A L Hendriks et al.
Introduction: People with haemophilia suffer from haemophilic joint disease that may result in physical inactivity and overweight. Shared medical appointments (SMAs) might help limit the consequences of haemophilic arthro...