14:00 - 14:15 Opening ceremony

Chairs: JJ Kiladjian (France) & C Harrison (United Kingdom)

14:15 - 15:45 SCIENTIFIC SESSION

Molecular pathogenesis and diagnosis

Chairs: JJ Kiladjian (France) & C Harrison (United Kingdom) 

• Molecular pathogenesis of MPN
  AR Green (United Kingdom)
• Practical use of molecular tests in MPN diagnosis and beyond
  R Skoda (Switzerland)
• New WHO proposals for diagnostic criteria of MPN
  T Barbui (Italy)
• Common mutations but many diseases unravelling the basis for phenotype
  I Plo (France)

09:00 - 11:00 CLINICAL CASES

Clinical Cases (interactive)

Chairs: G Birgegård (Sweden) & R Skoda (Switzerland)

• The young ET/PV patient
  JC Ianotto (France)
• Accelerated phase MF
  J Mascarenhas (USA)
• Guidelines for ET
  J Schwarz (Czech Republic)
• Pregnancy in ET
  M Griesshammer (Germany)
• Atypical CML
  A Almeida (Portugal)

09:00 - 11:00 SCIENTIFIC SESSION

State of the art in rare MPN

Chairs: T Devos (Belgium)

• Eosinophilia: unravelling the mystery
  A Reiter (Germany)
• Advances in the diagnosis and management of CMML
  A Almeida (Portugal)
• State of the art investigation and management of erythrocytosis 
  MF McMullin (United Kingdom)
• Novel data
  C Besses (Spain)
• Panel discussion
  All speakers

11:00 - 11:30 Coffee break

11:30 - 12:20 SCIENTIFIC SESSION

State of the art in rare MPN (continued)

Chairs: A Almeida (Portugal) & MF McMullin (United Kingdom)

• Mastocytosis: a complex but not so rare disease
  A Reiter (Germany)
• Familial MPN
  I Plo (France)