Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Anna Zaninoni"'
Autor:
Anna Zaninoni, Bruno Fattizzo, Loredana Pettine, Cristina Vercellati, Anna P. Marcello, Wilma Barcellini
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Autoimmune hemolytic anemia (AIHA) is due to autoantibodies with or without complement activation and involves cellular and cytokine dysregulation. Here, we investigated cytokine single-nucleotide polymorphisms (SNPs) of TNF-α, TGF-β1, IL-10, IL-6,
Externí odkaz:
https://doaj.org/article/0067351f118c44ec88bea0250cfa7556
Autor:
Anna Zaninoni, Roberta Marra, Elisa Fermo, Dario Consonni, Immacolata Andolfo, Anna Paola Marcello, Barbara Eleni Rosato, Cristina Vercellati, Wilma Barcellini, Achille Iolascon, Paola Bianchi, Roberta Russo
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Iron homeostasis and dyserythropoiesis are poorly investigated in pyruvate kinase deficiency (PKD), the most common glycolytic defect of erythrocytes. Herein, we studied the main regulators of iron balance and erythropoiesis, as soluble tran
Externí odkaz:
https://doaj.org/article/e45c108bc3d24e5782f00ae3ca79ea19
Autor:
Bruno Fattizzo, Cristina Vercellati, Anna Marcello, Parija Patel, Megan Wind-Rotolo, Loredana Pettine, Simona Leoni, Elisa Fermo, Paola Bianchi, Anna Zaninoni, Wilma Barcellini
Publikováno v:
HemaSphere, Vol 7, p e07083ab (2023)
Externí odkaz:
https://doaj.org/article/50947a31378f4de693a9865969a01c66
Autor:
Michele Sorrenti, Davide Murgia, Loredana Pettine, Giacinto Pedone, Anna Zaninoni, Wilma Barcellini, Bruno Fattizzo
Publikováno v:
HemaSphere, Vol 7, p e3553938 (2023)
Externí odkaz:
https://doaj.org/article/0928c5d7f8b24294b8daa1882dcef8ab
Autor:
Francesco Versino, Nicoletta Revelli, Stefania Villa, Loredana Pettine, Anna Zaninoni, Daniele Prati, Wilma Barcellini, Bruno Fattizzo
Publikováno v:
HemaSphere, Vol 7, p e19974a4 (2023)
Externí odkaz:
https://doaj.org/article/4104d7eeef86488a996619900579d64a
Autor:
Paola Bianchi, Azita Sharif, Cristina Vercellati, Elisa Fermo, Maria Laura Chiaretto, Anna Paola Marcello, Anna Zaninoni, Nadi Mirra, Simona Torricelli, Virna De Zordi, Stefania Bottalico, Wilma Barcellini, Ferruccio Ceriotti, Anna Chiara Migliorini
Publikováno v:
HemaSphere, Vol 7, p e97495be (2023)
Externí odkaz:
https://doaj.org/article/6c4e920a9f204f77a178f4e3468f9c59
Autor:
Bruno Fattizzo, Francesco Versino, Anna Zaninoni, Anna Paola Maria Luisa Marcello, Cristina Vercellati, Silvia Artuso, Wilma Barcellini
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
More than half of patients with paroxysmal nocturnal hemoglobinuria (PNH) treated with complement fraction C5 inhibitors experience residual anemia and hemolysis. This is partly due to the persistent activation of the complement cascade upstream C5,
Externí odkaz:
https://doaj.org/article/1a370f2fd0fd4556ae115c6a51a8a932
Autor:
Cristina Vercellati, Anna Paola Marcello, Bruno Fattizzo, Anna Zaninoni, Agostino Seresini, Wilma Barcellini, Paola Bianchi, Elisa Fermo
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
We investigated by targeted next generation sequencing the genetic bases of hereditary spherocytosis in 25 patients and compared the molecular results with the biochemical lesion of RBC membrane obtained by SDS-PAGE analysis. The HS diagnosis was bas
Externí odkaz:
https://doaj.org/article/21299625cbbe4185b034bf08490ad166
Autor:
Bruno Fattizzo, Giorgia Virginia Levati, Juri Alessandro Giannotta, Giulio Cassanello, Lilla Marcella Cro, Anna Zaninoni, Marzia Barbieri, Giorgio Alberto Croci, Nicoletta Revelli, Wilma Barcellini
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Low-risk myelodysplastic syndromes (LR-MDS) are a very heterogeneous disease, with extremely variable clinical features and outcome. Therapeutic strategies are still limited and mainly consist of erythropoiesis-stimulating agents (ESAs) and transfusi
Externí odkaz:
https://doaj.org/article/d5f012f1e2de4ebc9563150edf185ee7
Autor:
Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Ebru Yilmaz Keskin, Silverio Perrotta, Anna Zaninoni, Valentina Brancaleoni, Alberto Zanella, Juri A. Giannotta, Wilma Barcellini, Paola Bianchi
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Congenital hemolytic anemias (CHAs) are heterogeneous and rare disorders caused by alterations in structure, membrane transport, metabolism, or red blood cell production. The pathophysiology of these diseases, in particular the rarest, is often poorl
Externí odkaz:
https://doaj.org/article/96eeaebcf4f543c6b7485b7d215fce35