
Diagnóstico de Hemofilia e Outros Distúrbios Hemorrágicos: Manual de Laboratório, terceira edição
A 3ª edição do Manual de Laboratório da WFH é o guia definitivo para o diagnóstico preciso da hemofilia e
Year:
Language: English
Author(s): World Federation of Hemophilia
This session from the WFH 2020 Virtual Summit was developed as an educational response to the COVID-19 pandemic for the global bleeding disorders community. Speakers Radoslaw Kaczmarek, Flora Peyvandi, Cedric Hermans and Mark Skinner discuss the pathophysiology and clinical manifestations of COVID-19, practical advice on the management of COVID-19, and safety and supply of plasma derived products during the pandemic.
The WFH does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, the WFH recommends that you contact your physician or local treatment centre. Before administering any products, the WFH urges patients to check dosages with a physician or hemophilia centre staff, and to consult the pharmaceutical company’s printed instructions.
The WFH does not promote any particular pharmaceutical product and any mention of any commercial brand in this presentation is strictly for educational purposes.

A 3ª edição do Manual de Laboratório da WFH é o guia definitivo para o diagnóstico preciso da hemofilia e

People with bleeding disorders continue to face significant challenges in diagnosis, access to treatment and care around the world. To

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

This information sheet is designed to help understand the similarities, differences, and current state of knowledge for the existing genetic