Massimo Maffei

7PUBLICATIONS
30CO-AUTHORS
HaematologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Feb 02, 2026
Familial erythrocytosis and phenotypic heterogeneity associated with different defects in alpha globin genes: a significant new case of Hb Wroclaw (α88(F9) Ala>Glu; HBA1: c.266C>A).

Valentina Carrai, Cristina Giubbilei, Tiziana Biagioli

|Aug 14, 2025
Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia.

Gianluca Dell'Orso, Tommaso Passarella, Serena Cappato

|Jan 25, 2025
Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs.

Rita Selvatici, Valentina Guida, Massimo Maffei

|Dec 17, 2024
Hb A2-Pontedera [δ93(F9) Cys > Trp; HBD: C.282T > G]: A New δ-Globin Chain Variant Detected by Screening Tests for Hemoglobinopathies.

Massimo Maffei, Massimo Mogni, Serena Manzini

|Nov 11, 2024
Ability of the Capillary Electrophoresis-based HbA1c Assay to Detect Rare Hemoglobin Variants.

Melania Olivieri, Marco Rosetti, Giovanni Poletti

|Sep 15, 2022
Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary Electrophoresis.

Lara Calcagno, Maria M Ciriello, Monica Maccarini

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Frequent Collaborators

5 joint publications

Domenico Coviello

2 joint publications

Cristina Curcio

1 joint publications

Valeria Maria Pinto

1 joint publications

Melania Olivieri