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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
Yi Hu,Dasheng Luo,Defu Yu Yi Hu
Background: Haemophilic arthropathy (HA) is a common complication of haemophilia, characterized by progressive joint degeneration due to recurrent bleeding. Iron overload from erythrocyte lysis is thought to play a key ro...
Sylvia von Mackensen,Carolin Moorthi,Ronald Fischer et al. Sylvia von Mackensen et al.
Introduction: Assessment of health-related quality of life (HRQoL) is relatively new in von Willebrand disease (VWD). So far, generic questionnaires have mainly been used for HRQoL assessment in VWD. ...
Seyed Mohammad Javad Mortazavi,Babak Haghpanah,Mohammadhasan Kaseb et al. Seyed Mohammad Javad Mortazavi et al.
Aim: This study aims to evaluate the natural course and resolution of flexion contracture following total knee arthroplasty (TKA) in individuals with haemophilic arthropathy. ...
Klaudia Paczóska,Wanda Badowska,Halina Bobrowska et al. Klaudia Paczóska et al.
Background: Modern prophylaxis in haemophilia aims not only to prevent bleeding but also to ensure a quality of life (QoL) comparable to healthy peers. Real-world data on health-related QoL (HRQoL) in children receiving p...
Jelien den Hollander,Marjon H Cnossen,Ron A A Mathôt Jelien den Hollander
Introduction: Efanesoctocog alfa is a novel factor VIII (FVIII) concentrate with a unique molecular design that enables Von Willebrand Factor-independent clearance in patients with haemophilia A. Limited sampling strategi...
Nita Radhakrishnan,Archit Pandharipande,Ritu Gupta et al. Nita Radhakrishnan et al.
Background: In India, persons with haemophilia (PWH) are entitled to free diagnostic services, clotting-factor concentrates and physiotherapy. However, families often continue to experience substantial financial hardships...
Divyaswathi Citla-Sridhar,Daniel Liu Divyaswathi Citla-Sridhar
Background: Glanzmann Thrombasthenia (GT) is a rare autosomal recessive bleeding disorder characterised by defective platelet aggregation due to abnormalities in the glycoprotein IIb/IIIa complex. With a lack of large rea...
Susan Halimeh,Cornelia Wermes,Carolin Moorthi et al. Susan Halimeh et al.
Introduction: Von Willebrand disease (VWD) is one of the most common hereditary disorders of primary haemostasis. Females with VWD often report heavy menstrual bleeding (HMB) that can significantly impact health-related q...
Ze Chen,Guiyong Jiang,Yaowen Xu et al. Ze Chen et al.
Introduction: Achilles tendon lengthening combined with external fixation (EF) has shown promising outcomes in managing haemophilia-related Achilles tendon contracture. ...