Results 91 to 100 of about 32,062 (289)
Meeting the challenges of haemophilia care and patient support in China and Brazil
, 2015 . Projects are underway in many developing countries to try to improve the provision of treatment and access to care for people with haemophilia (PWH), as long-term prophylactic treatment, which improves quality of life for PWH, is still restricted to ...
Ozelo, MC, Matta, MAP, Yang, RC
core +1 more source
A longitudinal study of family structure in Swedish persons with haemophilia
, 2014 Haemophilia is an X-linked inherited rare bleeding disorder affecting mainly men. The treatment consists of replacement therapy that has been associated with severe side effects, such as blood transmitted viral infections, but has markedly improved over ...
Berntorp, Erik, +6 more
core +2 more sources
Real-world comparative analysis of bleeding complications and health-related quality of life in patients with haemophilia A and haemophilia B. [PDF]
, 2018 Clinical severity and impact of haemophilia on quality of life have been generally considered to be lower for haemophilia B (HB) compared with haemophilia A (HA) patients. To compare annual bleeding rate (ABR), target joint development and health-related
O'Hara, Jamie +13 more
core +1 more source
Performing Large‐Scale Genetic Analysis in the Bleeding Disorders Community
Haemophilia, EarlyView.ABSTRACT Inherited bleeding disorders encompass a diverse group of conditions caused by genetic defects affecting coagulation factors, fibrinogen, von Willebrand factor, or platelet function. Despite major advances in quantitative and functional laboratory assays, a substantial diagnostic gap remains, particularly in patients with mild or atypical ...
Anna R. Blankstein +6 more
wiley +1 more source
Recommendations for assessment, monitoring and follow-up of patients with haemophilia
, 2011 Over the last few decades, clinical follow-up of patients with haemophilia has become more complex as a result of the introduction of new treatment strategies, the presence of comorbidities related to haemophilia or ageing, as well as the emergence of ...
Astermark, Jan +27 more
core +1 more source
Haemophilia, EarlyView.ABSTRACT Rare bleeding disorders (RBDs) represent a diverse group of inherited conditions involving coagulation factors or platelets. These conditions, such as Glanzmann thrombasthenia (GT) or severe coagulation factor deficiencies, are uncommon. In contrast, bleeding disorder of unknown cause (BDUC) is a diagnosis of exclusion without an identifiable ...
Alessandro Casini +4 more
wiley +1 more source
Musculoskeletal evaluation in severe haemophilia A patients from Latin America
, 2015 There is a paucity of literature on haemophilia treatment in Latin American countries, a region characterized by rapidly improving systems of care, but with substantial disparities in treatment between countries. The aim of this study was to evaluate the
Chumpitaz, G +11 more
core +1 more source
Patient Preferences for the Treatment of Haemophilia A and B in France
Haemophilia, EarlyView.ABSTRACT Introduction Haemophilia impacts health and quality of life. Advances in treatments such as factor replacement therapy (FRT), bispecific monoclonal antibody (BS‐mAb), gene therapy (GT), rebalancing treatment and high sustained factor necessitate understanding patient preferences to inform therapeutic strategies. Aim This study quantified trade‐
Yesim Dargaud +10 more
wiley +1 more source
Khyber Medical University JournalOBJECTIVE: To investigate the association between coping strategies, meaning in life, and health-related quality of life (HRQoL) among young adults with haemophilia. METHODS: This cross-sectional study was conducted from February 2023 to August 2023 at
Zoya Zeeshan Rao, Saima Ahmad
doaj +1 more source