Progressive joint destruction resulting from intra-articular bleeding is the major morbidity affecting patients with haemophilia (PWH), particularly those with inhibitors. Advances in understanding the detrimental processes set in motion by the exposure of joints to bleeding have shaped current management methods. However, to achieve optimal joint health in PWH, in addition to achieving haemostasis at the bleeding vessel, it may be appropriate to explore experimentally other conceptual frameworks. These include the possibilities that markers might help to identify individuals at the risk of more rapid joint deterioration, that clotting factors may have additional local action within tissues, and that outcomes might be improved with therapie...
Hemophilia is a hereditary coagulation disorder caused by a deficiency of either blood coagulation f...
Hemophilia is an X-linked heritable coagulopathy with an overall prevalence of approximately 1 in 10...
Hemophilia is a hematological disorder characterized by a partial or complete deficiency of clotting...
The inherited coagulation disorder haemophilia is characterized by spontaneous and trauma-related bl...
Although effective therapies for haemophilia have been available for decades, the prevention and tre...
Abstract: In patients with haemophilia, regular replacement therapy with clotting factor concentrate...
In patients with haemophilia, regular replacement therapy with clotting factor concentrates (prophyl...
Haemarthroses cause major morbidity in patients with haemophilia. Blood has devastating effects on a...
Haemarthroses cause major morbidity in patients with haemophilia. Blood has devastating effects on a...
Haemophilia is characterized by bleeding longer after an injury, easy bruising, and an increased ris...
Musculoskeletal bleeding is the hallmark of hemophilia and cannot be completely prevented despite cl...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Musculoskeletal bleeding is the hallmark of hemophilia and cannot be fully prevented by prophylactic...
Background: Patients with haemophilia experience recurring hemarthroses, mainly involving knees, elb...
Hemophilia is a congenital clotting factor deficiency characterized by spontaneous and trauma-relate...
Hemophilia is a hereditary coagulation disorder caused by a deficiency of either blood coagulation f...
Hemophilia is an X-linked heritable coagulopathy with an overall prevalence of approximately 1 in 10...
Hemophilia is a hematological disorder characterized by a partial or complete deficiency of clotting...
The inherited coagulation disorder haemophilia is characterized by spontaneous and trauma-related bl...
Although effective therapies for haemophilia have been available for decades, the prevention and tre...
Abstract: In patients with haemophilia, regular replacement therapy with clotting factor concentrate...
In patients with haemophilia, regular replacement therapy with clotting factor concentrates (prophyl...
Haemarthroses cause major morbidity in patients with haemophilia. Blood has devastating effects on a...
Haemarthroses cause major morbidity in patients with haemophilia. Blood has devastating effects on a...
Haemophilia is characterized by bleeding longer after an injury, easy bruising, and an increased ris...
Musculoskeletal bleeding is the hallmark of hemophilia and cannot be completely prevented despite cl...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Musculoskeletal bleeding is the hallmark of hemophilia and cannot be fully prevented by prophylactic...
Background: Patients with haemophilia experience recurring hemarthroses, mainly involving knees, elb...
Hemophilia is a congenital clotting factor deficiency characterized by spontaneous and trauma-relate...
Hemophilia is a hereditary coagulation disorder caused by a deficiency of either blood coagulation f...
Hemophilia is an X-linked heritable coagulopathy with an overall prevalence of approximately 1 in 10...
Hemophilia is a hematological disorder characterized by a partial or complete deficiency of clotting...