Year: 2023
Language: English
This resource is also available in:
Also Available In: Japanese
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Traditional Chinese
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of rare coagulation factor deficiencies.
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia
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
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the