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Check out the latest articles on von Willebrand disease

Last update : Monday April 15, 2024

How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause

Evaluating a patient suspected of having a mild to moderate bleeding disorder (MBD) is one of the more challenging tasks in hematology. Many features of the bleeding history are subjective, distinguishing...
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International Journal of Laboratory Hematology 2024; AOP: 10.1111/ijlh.14266
Alessandro Casini et al.

Use of crushed tranexamic acid tablets in water for paediatric patients with bleeding disorders

Antifibrinolytic agents are frequently used to treat patients with bleeding disorders. These agents are lysine analogues that exert their haemostatic effects by binding to plasminogen and inhibiting its...
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Haemophilia 2024; AOP: 10.1111/hae.14996
Ahmad Al‐Huniti et al.

Diagnosis and treatment challenges in lower resource countries: State‐of‐the‐art

In the last several decades, the bleeding disorders community has seen an unprecedented evolution of novel therapies for treating inherited disorders. These therapies have included recombinant clotting...
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Haemophilia 2024; AOP: 10.1111/hae.14956
Johnny Mahlangu et al.

Von Willebrand Disease and Pregnancy: Management Protocol From Labor to the Postpartum Period.

Von Willebrand disease (VWD) is a hemostatic disorder characterized by a quantitative or qualitative deficiency of the Von Willebrand factor (VWF). It affects males and females equally. This pathology has more severe clinical manifestations in females of reproductive age, with a mean age of diagnosis at 19 years. In the pregnant patient, Von Willebrand disease poses an increased risk of complications during labor or the postpartum period, attributed...
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Cureus 2024 Feb; 16(2): e53465
Muoz Vargas Brandon Alejandro et al.

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