Year: 2009
Language: Japanese
Author(s): World Federation of Hemophilia
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Traditional Chinese
この患者向けハンドブックには、稀な凝固因子欠乏症の遺伝特性、診断、症状、管理についての基本情報が記載されています。
Also Available In: Japanese This resource has also been translated into the following languages, with permission from the WFH, by
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of inherited platelet function disorders.
In these sessions from the WFH 2022 World Congress, David Lillicrap, Len Valentino, Sophie Susen, Mrinal Gounder, Rebecca Kruse-Jarres, Christine
In the Monday afternoon session entitled Rare Bleeding Disorders, Gillian Gidley reviews the genotypes and phenotypes associated with FXI deficiency,
In the Monday afternoon session entitled Rare Bleeding Disorders, Flora Peyvandi gives an overview of RBDs in Europe and discusses
Adapted from: Global NMO Training 2016 plenary presentation by Glenn PierceReviewed by: Glenn PierceEdited by: Georghia Michael This first eLearning
