MPN&MPNr-EuroNet Twelfth Meeting May 10-12, 2017

Diagnostic of Sporadic and Hereditary Myeloproliferative Diseases

The aims of MPN&MPNr-EuroNet's twelfth meeting to be held in Göteborg, Sweden, on May 10-12, 2017 are: 

To share information on the newest developments in MPNs and related congenital diseases, hereditary erythrocytosis and hereditary thrombocytosis;
To exchange and diffuse the latest information and recommendations on the molecular assays developed for diagnosis or research in laboratories working on MPNs and related diseases across Europe. NGS will be a special focus of this meeting;
To provide recommendations for the molecular diagnosis of MPN, hereditary erythrocytosis and hereditary thrombocytosis;
To discuss and plan for the various tasks and objectives of the three MPN&MPNr-EuroNet working groups (WG);
To help and mentor young scientists interested in MPNs.

To do so, abstracts will be selected for short talks in the different sessions. Posters will be presented during the whole length of the meeting.

Plenary sessions will cover the newest knowledge in MPNs. Each WG will convene under the direction of the WG chairs. New participants are encouraged to become actively involved in specific WG tasks.

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