Immacolata Andolfo

27PUBLICATIONS
68CO-AUTHORS
Adolescent healthEpigenetics (incl. genome methylation and epigenomics)Microelectromechanical systems (MEMS)Mineral processing/beneficiationMolecular targets
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Publications (27)

|Apr 22, 2026
Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrum.

|Apr 21, 2026
Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red blood cell and iron disorders.

|Feb 09, 2026
Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias.

Antonella Nostroso, Roberta Marra, Barbara Eleni Rosato

|Nov 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis.

Barbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra

|Jul 16, 2024
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia.

Achille Iolascon, Immacolata Andolfo, Roberta Russo

|May 30, 2024
Targeting ATP2B1 impairs PI3K/Akt/FOXO signaling and reduces SARS-COV-2 infection and replication.

Pasqualino de Antonellis, Veronica Ferrucci, Marco Miceli

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Frequent Collaborators

23 joint publications

Roberta Russo

14 joint publications

Achille Iolascon

5 joint publications

Mario Capasso

4 joint publications

Gian Luca Forni