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EHA-JSH Travel Grant
Financial support to help EHA members under 40 attend the Japanese Society of Hematology's Annual Meeting in October 2024.
Read moreSWG Preceptorship Program
Funding to enable an SWG create its own preceptorship—and promote learning and innovation in our community. The call for proposals closed at 12:00 CEST on March 28, 2025.
Read moreWithout access to treatment, can we truly innovate in rare diseases?
Interview with Giampaolo Merlini
There have been many developments on rare diseases since the EU Orphan Medicinal Products Regulation came into force in 2000. As the European Commission is evaluating its effectiveness, EHA discussed with Prof.
EBAH CME policy
Welcome to the EBAH CME Accreditation policy for EHA2025 Congress. Below you will find an overview of the EBAH CME credits that can be collected for physical attendance as well as virtual attendance of the sessions.
Read moreHow to apply
The CRTH 2025 call for applications is now closed. Timelines
Application CRTH 2025
Deadline: September 24, 2024 (15:00 CEST)
Notification
November 2024
Questions: training@ehaweb. orgDownload the Signature letter template.
EHA-ASH Translational Research Training in Hematology
How to apply for TRTH 2026
The application process for TRTH 2026 is being managed by the American Society of Hematology (ASH).
Meet Robin Foà, our Volunteer of the Month
Can you tell us what you do for EHA and when you started?
I have been a member of EHA from its beginning and have participated in all EHA Congresses.
Meet Robin Foà, our Volunteer of the Month
Can you tell us what you do for EHA and when you started?
I have been a member of EHA from its beginning and have participated in all EHA Congresses.
A new form of inherited thrombocytopenia (ETV6-related thrombocytopenia, ETV6-RT): NEVER JUDGE A BOOK BY ITS COVER!
A new form of inherited thrombocytopenia (ETV6-related thrombocytopenia, ETV6-RT): NEVER JUDGE A BOOK BY ITS COVER!
We recently discovered a new form of an inherited deficiency of platelets (inherited thrombocytopenia-IT), which is caused by mutations in the ETV6-gene.
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