Maria Rita Gamberini
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Explore the profile of Maria Rita Gamberini including associated specialties, affiliations and a list of published articles.
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56
Citations
979
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Recent Articles
1.
Gianesin B, Piel F, Musallam K, Barella S, Casale M, Cassinerio E, et al.
Haematologica
. 2025 Jan;
PMID: 39844751
Not available.
2.
Gambari R, Gamberini M, Cosenza L, Zuccato C, Finotti A
J Clin Med
. 2025 Jan;
14(1.
PMID: 39797371
: Cellular biobanks are of great interest for performing studies finalized in the development of personalized approaches for genetic diseases, including β-thalassemia and sickle cell disease (SCD), important diseases affecting...
3.
Zurlo M, Zuccato C, Cosenza L, Gamberini M, Finotti A, Gambari R
J Clin Med
. 2024 May;
13(9).
PMID: 38731008
: in β-thalassemia, important clinical complications are caused by the presence of free α-globin chains in the erythroid cells of β-thalassemia patients. These free α-globin chains are present in excess...
4.
Zurlo M, Zuccato C, Cosenza L, Gasparello J, Gamberini M, Stievano A, et al.
Int J Mol Sci
. 2023 Oct;
24(20).
PMID: 37894732
The β-thalassemias are hereditary monogenic diseases characterized by a low or absent production of adult hemoglobin and excess in the content of α-globin. This excess is cytotoxic for the erythroid...
5.
Gambari R, Zuccato C, Cosenza L, Zurlo M, Gasparello J, Finotti A, et al.
Biology (Basel)
. 2023 Sep;
12(9).
PMID: 37759601
In this review article, we present the fascinating story of rapamycin (sirolimus), a drug able to induce γ-globin gene expression and increased production of fetal hemoglobin (HbF) in erythroid cells,...
6.
Meloni A, Pistoia L, Lupi A, Righi R, Vallone A, Missere M, et al.
Tomography
. 2023 Sep;
9(5):1711-1722.
PMID: 37736989
Background: The E-MIOT (Extension-Myocardial Iron Overload in Thalassemia) project is an Italian Network assuring high-quality quantification of tissue iron overload by magnetic resonance imaging (MRI). We evaluated the impact of...
7.
Gamberini M, Zuccato C, Zurlo M, Cosenza L, Finotti A, Gambari R
Hematol Rep
. 2023 Jul;
15(3):432-439.
PMID: 37489374
The β-thalassemias are a group of monogenic hereditary hematological disorders caused by deletions and/or mutations of the β-globin gene, leading to low or absent production of adult hemoglobin (HbA). For...
8.
Meloni A, Pistoia L, Gamberini M, Spasiano A, Cuccia L, Allo M, et al.
Eur J Intern Med
. 2023 May;
114:93-100.
PMID: 37150716
Background: No study has evaluated the effect of hepatitis C virus (HCV) infection on the wide spectrum of complications affecting patients with thalassemia. Objectives: This multicenter study prospectively assessed the...
9.
Origa R, Gianesin B, Longo F, Di Maggio R, Cassinerio E, Gamberini M, et al.
Cancer
. 2023 Mar;
129(10):1616-1617.
PMID: 36917138
No abstract available.
10.
Meloni A, Pistoia L, Gamberini M, Cuccia L, Lisi R, Cecinati V, et al.
Diagnostics (Basel)
. 2023 Mar;
13(5).
PMID: 36900034
We assessed the prognostic value of multiparametric cardiovascular magnetic resonance (CMR) in predicting death from heart failure (HF) in thalassemia major (TM). We considered 1398 white TM patients (30.8 ±...