Report on the Annual Global Survey 2008
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.
Abstracts of the XXVIII International Congress of the World Federation of Hemophilia
This special issue of Haemophilia contains abstracts presented at the XXVIII WFH Congress, Istanbul, Turkey, 1-5 June 2008.
State of the Art XXVIII International Congress of the World Federation of Hemophilia
This special issue of Haemophilia contains reviews and original research reports from selected scientific sessions presented at the XXVIII WFH Congress, Istanbul, Turkey, 1-5 June 2008.
Report on the Annual Global Survey 2007
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.
Patient Outreach Guide for Hemophilia and Other Bleeding Disorders
This guide helps national hemophilia organizations plan and carry out an outreach campaign to identify people with hemophilia or other bleeding disorders who have not been diagnosed or are underserved by healthcare services.
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。
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 […]
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 – Japanese
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese 患者登録は、健康上の傾向のモニタリング、資源の割り当て、治療用製剤供給の調整および追跡、全国規模での購入プロセスの改善に極めて重要です。
Abstracts of the XXVII International Congress of the World Federation of Hemophilia
This special issue of Haemophilia contains abstracts presented at the XXVII WFH Congress, Vancouver, Canada, 21-25 May 2006.
State of the Art XXVII International Congress of the World Federation of Hemophilia
This special issue of Haemophilia contains reviews and original research reports from selected scientific sessions presented at the XXVII WFH Congress, Vancouver, Canada, 21-25 May 2006.