Academic title: PhD
Charge: Researcher associate
Which is your area of expertise for the "Disease/group of diseases"?
Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):
Hereditary anemia due to membrane defects, specially hereditary stomatocytosis, Molecular diagnosis and research on pathogenetic mechanism and new causative genes discovery.
Atypical hemolytic-uremic syndrome Hemoglobinopathy (Other than THAL and SCD) Hereditary elliptocytosis Hereditary spherocytosis Hereditary stomatocytosis Porphyrias Rare constitutional hemolytic anemia due to an enzyme disorder (Other than PKD) Rare constitutional hemolytic anemia due to pyruvate kinase deficiency
Which is your patient age coverage?
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Department of Laboratory Medicine||Dipartimento di Medicina di Laboratorio||Red blood cell defects, Bone marrow failure||AOU Federico II - Naples|