Year: 2009
Language: Japanese
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 patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia
Also Available In: Japanese This resource has also been translated into the following languages, with permission from the WFH, by
This edition is available in: English, Spanish, French The previous edition is also available in: Arabic, Russian, Simplified Chinese, Japanese
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of inherited platelet function disorders, including Bernard-Soulier
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the