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Acceptable, hopeful, and useful: development and mixed‑method evaluation of an educational tool about reproductive options for people with sickle cell disorder or trait

Early, M.L., Strodel, R.J., Lake, I.V. et al.
Sickle Cell Disease

Low von Willebrand Factor in Children and Adolescents: A Review

Srivaths L, Kouides PA
Von Willebrand Disease

Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States

Miller CH, Soucie JM, Byams VR, Payne AB, Sidonio RF Jr, Buckner TW, Bean CJ.
Acquired Hemophilia

A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH

van Galen KPM, d'Oiron R, James P, Abdul-Kadir R, Kouides PA, Kulkarni R, Mahlangu JN, Othman M, Peyvandi F, Rotellini D, Winikoff R, Sidonio RF.
Acquired Hemophilia

Is ≥ 100% the magic number to rule out the laboratory diagnosis of von Willebrand disease based on initial testing?

Weyand AC, Kouides P, Malvar J, Jaffray J.
LAN Developed Von Willebrand Disease

Standardizing care to manage bleeding disorders in adolescents with heavy menses—A joint project from the ISTH pediatric/neonatal and women’s health SSCs

Background Bleeding disorders (BD) are under-recognized in adolescents with heavy menstrual bleeding (HMB). Objectives The lack of clinical guidelines and variable symptomatic management of HMB…

Zia, A, Kouides, P, Khodyakov, D, et al.