Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Elisa Fermo"'
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:
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:
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:
Noémi B. A. Roy, Lydie Da Costa, Roberta Russo, Paola Bianchi, Maria del Mar Mañú-Pereira, Elisa Fermo, Immacolata Andolfo, Barnaby Clark, Melanie Proven, Mayka Sanchez, Richard van Wijk, Bert van der Zwaag, Mark Layton, David Rees, Achille Iolascon, on behalf of the British Society for Haematology and the European Hematology Association
Publikováno v:
HemaSphere, Vol 6, Iss 6, p e739 (2022)
Externí odkaz:
https://doaj.org/article/9374bbd49e7c4657be3e9a7c2dd0e7d2
Autor:
Achille Iolascon, Immacolata Andolfo, Roberta Russo, Wilma Barcellini, Elisa Fermo, Gergely Toldi, Stefano Ghirardello, Davis Rees, Richard Van Wijk, Antonis Kattamis, Patrick G. Gallagher, Noemi Roy, Ali Taher, Razan Mohty, Andreas Kulozik, Lucia De Franceschi, Antonella Gambale, Mariane De Montalembert, Gian Luca Forni, Cornelis L. Harteveld, Josef Prchal, Paola Bianchi, on behalf of SWG of Red Cell and Iron of EHA and EuroBloodNet
Publikováno v:
HemaSphere, Vol 5, Iss 12, p e660 (2021)
Externí odkaz:
https://doaj.org/article/fa52406ab7464209b23b224ac22e0faf
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
Autor:
Greta Simionato, Konrad Hinkelmann, Revaz Chachanidze, Paola Bianchi, Elisa Fermo, Richard van Wijk, Marc Leonetti, Christian Wagner, Lars Kaestner, Stephan Quint
Publikováno v:
PLoS Computational Biology, Vol 17, Iss 5, p e1008934 (2021)
The investigation of cell shapes mostly relies on the manual classification of 2D images, causing a subjective and time consuming evaluation based on a portion of the cell surface. We present a dual-stage neural network architecture for analyzing fin
Externí odkaz:
https://doaj.org/article/abbea161750f4e0c8f2d62cf2a7c9fcd
Autor:
Daniele Cattaneo, Giorgio Alberto Croci, Cristina Bucelli, Silvia Tabano, Marta Giulia Cannone, Gabriella Gaudioso, Maria Chiara Barbanti, Kordelia Barbullushi, Paola Bianchi, Elisa Fermo, Sonia Fabris, Luca Baldini, Umberto Gianelli, Alessandra Iurlo
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Lack of demonstrable mutations affecting JAK2, CALR, or MPL driver genes within the spectrum of BCR-ABL1-negative myeloproliferative neoplasms (MPNs) is currently referred to as a triple-negative genotype, which is found in about 10% of patients with
Externí odkaz:
https://doaj.org/article/d475a7f7136547a19dc24610dbb8620e
Autor:
Acaynne Lira Zidanes, Giacomo Marchi, Fabiana Busti, Alessandro Marchetto, Elisa Fermo, Alejandro Giorgetti, Alice Vianello, Annalisa Castagna, Oliviero Olivieri, Paola Bianchi, Domenico Girelli
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Iron loading anemias are characterized by ineffective erythropoiesis and iron overload. The prototype is non-transfusion dependent ß-thalassemia (NTDT), with other entities including congenital sideroblastic anemias, congenital dyserythropoietic ane
Externí odkaz:
https://doaj.org/article/2086565e089b4eceafd52f82c6fa3df4