Works by Mogni, Massimo

Results: 12

First Characterization of Human Amniotic Fluid Stem Cell Extracellular Vesicles as a Powerful Paracrine Tool Endowed with Regenerative Potential.

Published in:

Stem Cells Translational Medicine, 2017, v. 6, n. 5, p. 1340, doi. 10.1002/sctm.16-0297

By:

Balbi, Carolina;
Piccoli, Martina;
Barile, Lucio;
Papait, Andrea;
Armirotti, Andrea;
Principi, Elisa;
Reverberi, Daniele;
Pascucci, Luisa;
Becherini, Pamela;
Varesio, Luigi;
Mogni, Massimo;
Coviello, Domenico;
Bandiera, Tiziano;
Pozzobon, Michela;
Cancedda, Ranieri;
Bollini, Sveva

Publication type:

Article

Coinheritance of PIEZO1 variants and multi‐locus red blood cell defects account for the symptomatic phenotype in beta‐thalassemia carriers.

Published in:

American Journal of Hematology, 2023, v. 98, n. 6, p. E130, doi. 10.1002/ajh.26901

By:

Pinto, Valeria Maria;
Russo, Roberta;
Quintino, Sabrina;
Rosato, Barbara Eleni;
Marra, Roberta;
Del Giudice, Federica;
Mogni, Massimo;
Maffei, Massimo;
Iolascon, Achille;
Forni, Gian Luca;
Andolfo, Immacolata

Publication type:

Article

Hemoglobin Yamagata [β132(H10)Lys→Asn; (HBB: c.399A>T)]: a mosaic to be put together.

Published in:

Clinical Chemistry & Laboratory Medicine, 2021, v. 59, n. 10, p. 1670, doi. 10.1515/cclm-2021-0376

By:

Iacomelli, Iacopo;
Barberio, Giuseppina;
Pucci, Piero;
Monaco, Vittoria;
Maffei, Massimo;
Mogni, Massimo;
Curcio, Cristina;
Maoggi, Sauro;
Giulietti, Chiara;
Harteveld, Cornelis L.;
Ivaldi, Giovanni

Publication type:

Article

P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI‐LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA‐THALASSEMIA CARRIERS.

Published in:

HemaSphere, 2023, v. 7, p. 1, doi. 10.1097/01.HS9.0000972772.85628.08

By:

Maria Pinto, Valeria;
Russo, Roberta;
Quintino, Sabrina;
Eleni Rosato, Barbara;
Marra, Roberta;
Del Giudice, Federica;
Mogni, Massimo;
Maffei, Massimo;
Iolascon, Achille;
Luca Forni, Gian;
Andolfo, Immacolata

Publication type:

Article

Hemoglobin A 2 and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene.

Published in:

Genes, 2021, v. 12, n. 11, p. 1821, doi. 10.3390/genes12111821

By:

Mahmud, Noraesah;
Maffei, Massimo;
Mogni, Massimo;
Forni, Gian Luca;
Pinto, Valeria Maria;
Barberio, Giuseppina;
Ungari, Silvana;
Maffè, Antonella;
Curcio, Cristina;
Zanolli, Francesco;
Paventa, Raffaella;
Carta, Mariarosa;
Caleffi, Alberta;
Mercadanti, Mariella;
Maoggi, Sauro;
Ivaldi, Giovanni;
Coviello, Domenico

Publication type:

Article

Hb A<sub>2</sub>-Pontedera [δ93(F9) Cys > Trp; HBD: C.282T > G]: A New δ-Globin Chain Variant Detected by Screening Tests for Hemoglobinopathies.

Published in:

2024

By:

Maffei, Massimo;
Mogni, Massimo;
Manzini, Serena;
Murratzu, Clizia;
Stenner, Elisabetta;
Fiorini, Marcello;
Bacciardi, Paola;
Maoggi, Sauro;
Ivaldi, Giovanni;
Coviello, Domenico

Publication type:

Letter to the Editor

δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?

Published in:

Hemoglobin, 2024, v. 48, n. 5, p. 349, doi. 10.1080/03630269.2024.2414109

By:

Giubbilei, Cristina;
D'Angelo, Simona;
Fotzi, Ilaria;
Mogni, Massimo;
Guglielmelli, Paola;
Vannucchi, Alessandro Maria;
Carrai, Valentina

Publication type:

Article

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.

Published in:

Hemoglobin, 2022, v. 46, n. 4, p. 240, doi. 10.1080/03630269.2022.2118605

By:

Calcagno, Lara;
Ciriello, Maria M.;
Maccarini, Monica;
Mogni, Massimo;
Maffei, Massimo;
Barberio, Giuseppina;
Maoggi, Sauro;
Coviello, Domenico;
Ivaldi, Giovanni

Publication type:

Article

Hb A<sub>2</sub>-Pistoia [δ89(F5)Ser→Asn, HBD: c.269G>a]: a Novel Mutation on the δ-Globin Gene in an Italian Child.

Published in:

Hemoglobin, 2020, v. 44, n. 5, p. 368, doi. 10.1080/03630269.2020.1815766

By:

Guastini, Adriana;
Rizzi, Leonardo;
Santoni, Fabiano;
Mogni, Massimo;
Maffei, Massimo;
Vinci, Santina;
Barberio, Giuseppina;
Coviello, Domenico;
Ivaldi, Giovanni

Publication type:

Article

Next Generation Sequencing-Based Diagnosis in Thalassemia.

Published in:

2019

By:

Coviello, Domenico;
Maffei, Massimo;
Mogni, Massimo;
Mahmud, Noraesah

Publication type:

Abstract

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

Published in:

Genes, 2025, v. 16, n. 1, p. 28, doi. 10.3390/genes16010028

By:

Selvatici, Rita;
Guida, Valentina;
Maffei, Massimo;
Irrera, Milena Agata;
Margutti, Alice;
Bisceglia, Paola;
Mogni, Massimo;
Melchionda, Erica;
Stoico, Giuseppina;
Grifone, Nicoletta;
Bocciardo, Laura;
Salerio, Simone;
Nagliati, Vittoria;
Alberico, Angela;
Tringali, Giusy;
Melles, Cristina;
De Luca, Alessandro;
Ferlini, Alessandra;
Coviello, Domenico;
Curcio, Cristina

Publication type:

Article

Familial Robertsonian 13;14 Translocation With Mental Retardation and Epilepsy.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 6, p. 531, doi. 10.1177/08830738060210060701

By:

Buoni, Sabrina;
Zannolli, Raffaella;
Macucci, Francesca;
Pucci, Lucia;
Mogni, Massimo;
Pierluigi, Mauro;
Fois, Alberto

Publication type:

Article