Platelet Function Disorders
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Russian A discussion of platelet physiology and the mechanisms of platelet activation as pertains to the diagnosis and management of platelet function disorders.
Factor XI Deficiency and its Management
A comprehensive overview of factor XI deficiency, the most common of the rare bleeding disorders.
Protocols for the Treatment of Hemophilia and von Willebrand Disease
This monograph outlines the treatment protocol used by healthcare providers in Georgia, U.S.A., as an example of a strategy to provide quality standards of care for the management of hemophilia.
Hereditary Plasma Clotting Factor Disorders and their Management
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Russian This monograph provides an overview of the most common types of hereditary bleeding disorders, general principles of care, treatment options, and management of complications.
What is von Willebrand Disease? – Japanese
The 2023 edition is available in: English This edition is also available in: Spanish, French, Arabic, Russian, Simplified Chinese This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Farsi, Polish, Bengali, Setswana この患者向けハンドブックには、フォン・ヴィレブランド病の遺伝特性、診断、症状、管理についての基本情報が記載されています。
Advantages of a National Tender System for Clotting Factor Concentrates – Japanese
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese 国ごとの国家入札制度は、凝固因子製剤等の製品やサービスを購入するコスト効率の高い制度で、治療用製剤の需要や使用量の予測を促進し、より高水準な治療を可能にします。
What is von Willebrand Disease? – Polish
The 2023 edition is available in: English, Spanish, French This edition is also available in: Arabic, Russian, Simplified Chinese, Japanese This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Farsi, Bengali, Setswana This patient handbook contains basic information about the inheritance, diagnosis, symptoms and […]
What is von Willebrand Disease? – Farsi
The 2023 edition is available in: English, Spanish, French This edition is also available in: Arabic, Russian, Simplified Chinese, Japanese This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Polish, Bengali, Setswana This patient handbook contains basic information about the inheritance, diagnosis, symptoms and […]
Manufactured Shoes and Orthopedic Shoes – Japanese
Also Available In: English, Spanish This is not an official WFH translation. This resource has been translated with permission by a WFH National Member Organization (NMO), and is shared here with their kind permission. Translating organizations are encouraged to have translations reviewed by local experts, the WFH is not responsible for the translation or for […]
Report on the Annual Global Survey 2006
Compiled annually, the Annual Global Survey (AGS) provides demographic and other data on people with hemophilia, von Willebrand disease , other rare factor deficiencies, and inherited platelet disorders throughout the world.
Benefits of a National Patient Registry
Also Available In: Japanese Patient registries are crucial for monitoring trends in health, allocating resources, organizing and tracking distribution of treatment products, and improving the purchasing process on a national scale.
Proceedings of the WFH’s Fifth Global Forum on the Safety and Supply of Treatment Products for Bleeding Disorders
A summary of discussions held at the World Federation of Hemophilia’s Global Forum on the Safety and Supply of Hemophilia Treatment Products, which brings together patient groups, healthcare providers, regulators, industry representatives, and not-for-profit fractionators.