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    • Home
    • Diagnostics
      • Polycythemia Vera
      • Essential Thrombocythemia
      • Primary Myelofibrosis
      • Congenital Erythrocytosis
      • Hereditary Thrombocytosis
    • Molecular analyses
      • JAK2V617F
      • JAK2 Exon 12 mutations
      • Mpl/TPO_Receptor
      • Calreticulin (CALR)
      • Other genes mutated in MPN
      • EPO-Receptor
      • Oxygen sensing pathway genes
      • THPO
    • Events
    • Useful links
    • Members
    • Registration
    • INTRANET

      Events

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      • Munich, Germany – September 2011

      Munich, Germany – September 2011

      EVENT DESCRIPTION

      Participants to the twelfth MPN&MPNr-EuroNet meeting will have the opportunity to hear from international experts about the newest developments in the molecular diagnosis of MPNs and related congenital/hereditary diseases.

      EVENT CONTENT

      • to share information on the newest developments in MPN and related congenital diseases, congenital erythrocytosis and hereditary thrombocythemia;
      • to exchange and diffuse information on the molecular assays developed for diagnosis or research in laboratories working on MPN and related diseases across Europe;
      • to discuss and plan for the various tasks and objectives of the 4 working groups (WG).

      MORE INFORMATION

      Start Time

      4:00 pm

      September 14, 2011

      Finish Time

      2:00 pm

      September 16, 2011

      Address

      Max-Lebsche-Platz 31 81377 München, Germany

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      Former EU-sponsored COST Action BM0902 (2009-2013), a network of experts … “

      by MPN&MPNr-EuroNet.

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