Emanuele Tanzi
Overview
Explore the profile of Emanuele Tanzi including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
11
Followers
0
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Recent Articles
1.
Tanzi E, Di Modica S, Bordini J, Olivari V, Pagani A, Furiosi V, et al.
Am J Hematol
. 2024 Apr;
99(7):1313-1325.
PMID: 38629683
β-thalassemia is a disorder characterized by anemia, ineffective erythropoiesis (IE), and iron overload, whose treatment still requires improvement. The activin receptor-ligand trap Luspatercept, a novel therapeutic option for β-thalassemia, stimulates...
2.
Nai A, Cordero-Sanchez C, Tanzi E, Pagani A, Silvestri L, Di Modica S
Blood Cells Mol Dis
. 2023 Jun;
104:102761.
PMID: 37271682
β-Thalassemia is a genetic form of anemia due to mutations in the β-globin gene, that leads to ineffective and extramedullary erythropoiesis, abnormal red blood cells and secondary iron-overload. The severity...
3.
Olivari V, Di Modica S, Lidonnici M, Aghajan M, Cordero-Sanchez C, Tanzi E, et al.
Kidney Int
. 2023 Mar;
104(1):61-73.
PMID: 36990212
Anemia is a common complication of systemic inflammation. Proinflammatory cytokines both decrease erythroblast sensitivity to erythropoietin (EPO) and increase the levels of the hepatic hormone hepcidin, sequestering iron in stores...
4.
Di Modica S, Tanzi E, Olivari V, Lidonnici M, Pettinato M, Pagani A, et al.
Am J Hematol
. 2022 Sep;
97(10):1324-1336.
PMID: 36071579
β-thalassemia is a genetic disorder caused by mutations in the β-globin gene, and characterized by anemia, ineffective erythropoiesis and iron overload. Patients affected by the most severe transfusion-dependent form of...