Members

Name: Paola

Surname: Giordano

Academic title: Prof

Which is your area of expertise for the "Disease/group of diseases"?

• Diagnostics
• Treatment and care

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Clinical trial, Diagnosis, Treatment and Care

Disease groups:

Alpha- thalassaemia diseases Atypical hemolytic-uremic syndrome Beta-thalassemia and related diseases Hemoglobinopathy (Other than THAL and SCD) Hemophilia A Hemophilia B Hereditary elliptocytosis Hereditary spherocytosis Hereditary stomatocytosis Myeloproliferative neoplasm (Other than Chronic myeloid leukemia and Primary myelofibrosis) Porphyrias Rare constitutional aplastic anemia (Other than BDA, DKC, FA, SDS) Rare constitutional hemolytic anemia due to an enzyme disorder (Other than PKD) Rare constitutional hemolytic anemia due to pyruvate kinase deficiency Rare hemorrhagic disease due to constitutional coagulation factors defects (Other than Hemophilia and Von Willebrand disease) Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to an acquired platelet anomaly Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to quantitative platelet anomaly (High) Rare thrombotic disorder due to quantitative platelet anomaly (Low) Sickle cell disease and related diseases Typical hemolytic-uremic syndrome Von Willebrand disease

Which is your patient age coverage?

• Pediatrics

Member Representative

Subnetwork representative:

• Red blood cell defects