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Andolfo, Immacolata

About me

Name: Immacolata

Surname: Andolfo

Academic title: PhD

Charge: Researcher associate


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

  • Diagnostics

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.

Disease groups:

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?

  • Pediatrics



Webinars:

Member Go to Member

Name english: AOU Federico II - Naples

Name original: AOU Federico II di Napoli


Healthcare provider Go to healthcare provider

Name english: AOU Federico II - Naples

Name original: AOU Federico II di Napoli

Departments

English name Original name Subnetworks of expertise Healthcare provider