Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Barbara Gianesin"'
Autor:
Valeria Maria Pinto, Barbara Gianesin, Salvatore Sardo, Filippo Mazzi, Giammarco Baiardi, Sofia Menotti, Fabio Piras, Sabrina Quintino, Giacomo Robello, Francesca Mattioli, Gabriele Finco, Gian Luca Forni, Lucia De Franceschi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Pain is an hallmark of sickle-cell-related acute clinical manifestations as part of acute vaso-occlusive crisis (VOC). In SCD pain has different origins such as vascular or neuropathic pain, which requires multimodal analgesia. This is based
Externí odkaz:
https://doaj.org/article/7d0cb2daaaaf4f75969177fdc5fd3dc6
Autor:
Veronica Bordoni, Maddalena Casale, Valeria Maria Pinto, Rita Carsetti, Barbara Gianesin, Maria Rita Gamberini, Leila Mazdai, Susanna Barella, Anna Rita Denotti, Francesca Colavita, Silverio Perrotta, Aurelio Maggio, Lorella Pitrolo, Sabrina Quintino, Marco Caminati, Filippo Mazzi, Jacopo Ceolan, Lucia De Franceschi, Gian Luca Forni, Franco Locatelli, Chiara Agrati
Publikováno v:
HemaSphere, Vol 7, p e98163b7 (2023)
Externí odkaz:
https://doaj.org/article/61f3b3097b73470598f72a91beb56bfe
Autor:
Valeria Maria Pinto, Barbara Gianesin, Salvatore Sardo, Filippo Mazzi, Giammarco Baiardi, Sofia Menotti, Fabio Piras, Gabriele Finco, Gian Luca Forni, Lucia De Franceschi
Publikováno v:
HemaSphere, Vol 7, p e2003822 (2023)
Externí odkaz:
https://doaj.org/article/d6b333fde8a94cf38bd5dd1bfe3a40c9
Autor:
Valeria Maria Pinto, Lorenzo Bacigalupo, Barbara Gianesin, Andrea Cazzato, Sabrina Quintino, Gian Luca Forni
Publikováno v:
HemaSphere, Vol 7, p e9400165 (2023)
Externí odkaz:
https://doaj.org/article/3daac3a9862748f988c028bf7dfd2b48
Autor:
Valeria Maria Pinto, Barbara Gianesin, Frédéric B. Piel, Filomena Longo, Paolo Rigano, Alessandra Quota, Vincenzo Spadola, Giovanna Graziadei, Filippo Mazzi, Maria Domenica Cappellini, Aurelio Maggio, Antonio Piga, Lucia De Franceschi, Gian Luca Forni
Publikováno v:
Haematologica, Vol 108, Iss 4 (2022)
Externí odkaz:
https://doaj.org/article/dceb93b8ce9d46abba2232e2a4b8c515
Autor:
Giorgio Derchi, Khaled M. Musallam, Valeria Maria Pinto, Giovanna Graziadei, Marianna Giuditta, Susanna Barella, Raffaella Origa, Gavino Casu, Annamaria Pasanisi, Filomena Longo, Maddalena Casale, Roberta Miceli, Pierluigi Merella, Barbara Gianesin, Pietro Ameri, Immacolata Tartaglione, Silverio Perrotta, Antonio Piga, Maria Domenica Cappellini, Gian Luca Forni
Publikováno v:
Haematologica, Vol 107, Iss 7 (2022)
Externí odkaz:
https://doaj.org/article/cc1bf23e68984769acbf9393f0a002ab
Autor:
Giovanna Graziadei, Lucia De Franceschi, Laura Sainati, Donatella Venturelli, Nicoletta Masera, Piero Bonomo, Aurora Vassanelli, Maddalena Casale, Gianluca Lodi, Vincenzo Voi, Paolo Rigano, Valeria Maria Pinto, Alessandra Quota, Lucia D. Notarangelo, Giovanna Russo, Massimo Allò, Rosamaria Rosso, Domenico D'Ascola, Elena Facchini, Silvia Macchi, Francesco Arcioni, Federico Bonetti, Enza Rossi, Antonella Sau, Saveria Campisi, Gloria Colarusso, Fiorina Giona, Roberto Lisi, Paola Giordano, Gianluca Boscarol, Aldo Filosa, Sarah Marktel, Paola Maroni, Mauro Murgia, Raffaella Origa, Filomena Longo, Marta Bortolotti, Raffaella Colombatti, Rosario Di Maggio, Raffaella Mariani, Alberto Piperno, Paola Corti, Carmelo Fidone, Giovanni Palazzi, Luca Badalamenti, Barbara Gianesin, Frédéric B. Piel, Gian Luca Forni
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Sickle cell disease (SCD) is a worldwide distributed hereditary red cell disorder characterized by recurrent acute vaso-occlusive crises (VOCs and anemia). Gold standard treatments are hydroxycarbamide (HC) and/or different red blood cell (RBC) trans
Externí odkaz:
https://doaj.org/article/398e4c9f5e034cb4a3d5f9a863a7b433
Autor:
Gian Luca, Forni, Barbara, Gianesin, Khaled M, Musallam, Filomena, Longo, Rosamaria, Rosso, Roberto, Lisi, Maria Rita, Gamberini, Valeria Maria, Pinto, Giovanna, Graziadei, Angelantonio, Vitucci, Federico, Bonetti, Pellegrino, Musto, Antonio, Piga, Maria Domenica, Cappellini, Caterina, Borgna-Pignatti
Publikováno v:
American Journal of Hematology. 98:381-387
We report data on survival and complications for a longitudinal cohort of 709 transfusion-dependent β-thalassemia major patients (51.1% males) born between 1970 and 1997 and followed through 2020 at seven major centers in Italy. Overall survival pro
Autor:
Francesca Mattioli, Valeria Marini, Valeria Maria Pinto, Manuela Stella, Carmen Fucile, Francesca Lantieri, Giacomo Luci, Barbara Gianesin, Lorenzo Bacigalupo, Gian Luca Forni
Publikováno v:
Current Drug Metabolism. 23:1072-1079
Background: Iron-chelation therapy is life-saving in patients on a chronic transfusion regimen as it reduces organ damage related to iron deposition in the tissues. Deferasirox, an iron-chelator, is characterized by pharmacokinetics variability, and
Autor:
Rita Carsetti, Chiara Agrati, Valeria Maria Pinto, Barbara Gianesin, Rita Gamberini, Monica Fortini, Susanna Barella, Rita Denotti, Silverio Perrotta, Maddalena Casale, Aurelio Maggio, Lorella Pitrolo, Eleonora Tartaglia, Eva Piano Mortari, Francesca Colavita, Vincenzo Puro, Massimo Francalancia, Valeria Marini, Marco Caminati, Filippo Mazzi, Lucia De Franceschi, Gian Luca Forni, Franco Locatelli
Publikováno v:
Blood. 140:1735-1738
Patients with beta-thalassemia show 5-fold increase in agestandardized lethality due to SARS-CoV-2 infection, representing a high-risk population compared with age- and sex-matched healthy subjects.(1) Vaccination against SARS-CoV-2 is crucial to red