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Author(s): World Federation of Hemophilia,稀な凝固因子欠乏症とは
Format: Document
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。
This session from the WFH 2020 Virtual Summit was developed as an educational response to the COVID-19 pandemic for the
This workshop from the WFH 2020 Virtual Summit, presented by Ellia Tootoonchian, Mark Skinner, Donna Coffin, Alfonso Iorio, Emna Gouider-Belhadjali
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese, Japanese This is not an official WFH translation. This resource
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