Diagnosis of Hemophilia and Other Bleeding Disorders: A Laboratory Manual – Arabic
The 3rd edition is available in: English, Spanish Written and reviewed by the world’s leading experts in coagulation testing, this is the definitive, how-to guide for the accurate diagnosis of hemophilia and other bleeding disorders.
Guidelines for the Management of Hemophilia – Arabic
The 3rd edition has also been translated into the following languages, with permission from the WFH, by NMOs/Other Organizations: Georgian, Portuguese, Ukrainian The 2nd edition is available in: Simplified Chinese The 2nd edition has also been translated into the following languages, with permission from the WFH, by NMOs: Azerbaijani, Polish, Traditional Chinese This third edition, fully […]
Structure and Functions of Comprehensive Hemophilia Treatment Centres – Arabic
Also Available In: Japanese Access to a comprehensive hemophilia treatment centre (HTC) is a critical component of care. This fact sheet outlines how HTCs are set up and the ways in which they improve the overall health and well-being of patients with bleeding disorders.
What are Inherited Platelet Function Disorders? – Arabic
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of inherited platelet function disorders.
What are Rare Clotting Factor Deficiencies? – Arabic
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.
Patient Outreach Guide for Hemophilia and Other Bleeding Disorders – Arabic
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.
Advantages of a National Tender System for Clotting Factor Concentrates – Arabic
Also Available In: Japanese A national tender system is a cost-effective system for the purchase of products or services, such as clotting factor concentrates, that facilitates the prediction of demand and use of factor products and can lead to a higher standard of care.
What is von Willebrand Disease? – Arabic
This edition is also available in: Japanese This edition of this resource has also been translated into the following languages, with permission from the WFH, by NMOs: Farsi, Polish, Bengali, Setswana This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of von Willebrand disease.
Hemophilia in Pictures Educator’s Guide – Arabic
Also Available In: Japanese A companion to Hemophilia in Pictures, this Educator’s guide provides more detailed information for advanced learning. Also includes tips for effective patient education, key talking points, and review quizzes.
Benefits of a National Patient Registry – Arabic
Also Available In: Japanese Patient registries are crucial for monitoring trends in health, allocating resources, organizing and tracking distribution of treatment products, and improving the purchasing process on a national scale.
Hemophilia in Pictures – Arabic
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Estonian, Farsi, Greek, Indonesian, Italian, Macedonian, Polish, Portuguese, Sesotho, Vietnamese A colour-illustrated guide to hemophilia. It is the perfect educational tool for parents, nurses and other healthcare providers, and anyone seeking to transmit basic information about hemophilia and its […]
Guide to Developing a National Patient Registry – Arabic
Having a national patient registry means being able to answer fundamental questions about the hemophilia population within a given country. This step-by-step guide outlines the basic principles of data collection, maintenance, and analysis and compares different types of registries.