Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Carmelo, Fidone"'
Autor:
Maria Denaro, Elisa Ferro, Giuseppe Barrano, Salvatore Meli, Mariangela Busacca, Damiano Corallo, Alessia Capici, Alessandra Zisa, Luana Cucuzza, Sandra Gradante, Marialuisa Occhipinti, Paola Santalucia, Raffaele Elia, Angelo Aliquò, Daniele Tibullo, Carmelo Fidone, Vincenzo Bramanti
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4742 (2023)
The coronavirus disease 19 (COVID-19) post pandemic evolution is correlated to the development of new variants. Viral genomic and immune response monitoring are fundamental to the surveillance of severe acute respiratory syndrome coronavirus 2 (SARS-
Externí odkaz:
https://doaj.org/article/27a2e0bf7b7b482e8ebf6a01bb945669
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:
Giovanna Russo, Lucia De Franceschi, Raffaella Colombatti, Paolo Rigano, Silverio Perrotta, Vincenzo Voi, Giovanni Palazzi, Carmelo Fidone, Alessandra Quota, Giovanna Graziadei, Antonello Pietrangelo, Valeria Pinto, Giovan Battista Ruffo, Francesco Sorrentino, Donatella Venturelli, Maddalena Casale, Francesca Ferrara, Laura Sainati, Maria Domenica Cappellini, Antonio Piga, Aurelio Maggio, Gian Luca Forni
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS). Clinical manifestations of SCD are mainly characterized by chronic hemolysis and acute vaso-oc
Externí odkaz:
https://doaj.org/article/4eb86eed929a495c968f5398eba2981d
Autor:
Sabrina Quintino, Filomena Longo, Maurizio Miano, Vincenzo Voi, Maria Caterina Putti, Margerita Migone De Amicis, Monica Fortini, Susanna Barella, Barbara Gianesin, Federico Bonetti, Andrea Beccaria, Manuela Balocco, Andrea Piolatto, Saveria Campisi, Rosamaria Rosso, Angelantonio Vitucci, Valentina Carrai, Alessandra Quota, Zelia Borsellino, Antonio Piga, Maddalena Casale, Anna Rita Denotti, Michela Ribersani, Maria Rita Gamberini, Domenico Roberti, Alberto Piperno, Roberto Lisi, Carmelo Fidone, Maria Domenica Cappellini, Sabrina Bagnato, Anna De Giovanni, Micol Quaresima, Valeria Maria, Lorella Pitrolo, Marco Marziali, Giovanna Graziadei, Carmen Gaglioti, Aldo Filosa, Chiara Dal Zotto, Lucia De Franceschi, Irene Motta, Immacolata Tartaglione, Francesco Arcioni, Aurelio Maggio, Marilena Serra, Giovan Battista Ruffo, Massimo Gentile, Elisa De Michele, Anna Spasiano, Paolo Ricchi, Antonella Massa, Silverio Perrotta, R. Mariani, Gian Luca Forni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e77154d342eff5f5889b25c798571759
http://hdl.handle.net/11591/458236
http://hdl.handle.net/11591/458236
High Dickkopf-1 levels are associated with chronic inflammation in children with sickle cell disease
Autor:
Paola Giordano, Giovanni Carlo Del Vecchio, Giovanna Russo, Viviana Valeria Palmieri, Laura Piacente, Carmelo Fidone, Flavia Urbano, Maria Felicia Faienza
Publikováno v:
European journal of haematologyREFERENCES. 108(4)
Sickle bone disease (SBD) is a chronic complication of sickle cell disease (SCD) whose pathogenesis is not completely understood. Chronic inflammation associated with SCD could alter bone remodeling. Our aim was to analyze the serum levels of bone re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9114f5444d06e753fe005af6d09eab8
https://pubmed.ncbi.nlm.nih.gov/34962669
https://pubmed.ncbi.nlm.nih.gov/34962669
Autor:
Maria Rita Gamberini, Roberto Lisi, Zelia Borsellino, Maddalena Casale, Maurizio Mangione, Massimo Allò, Maria Caterina Putti, Alessia Pepe, Massimo Midiri, Carmelo Fidone, Vincenzo Positano, Laura Pistoia, Antonella Quarta, Tommaso Casini, Domenico Giuseppe D'Ascola, Aldo Filosa, Gennaro Restaino, Antonella Meloni
Publikováno v:
JACC: Cardiovascular Imaging. 13:1284-1286
A retrospective magnetic resonance imaging (MRI) study on a large cohort of children with thalassemia major (TM) showed cardiac involvement by early childhood; 21% of children presented with abnormal cardiac T2* and 16% with cardiac fibrosis. Moreove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80c2ceb46b7df87761d438d6d92794c9
https://doi.org/10.1016/j.jcmg.2019.12.015
https://doi.org/10.1016/j.jcmg.2019.12.015
Autor:
Ibrahim El-Battrawy, Elisa De Michele, Manuela Balocco, Immacolata Tartaglione, Carmelo Fidone, Roberto Lisi, Maria Caterina Putti, Marcos Garca-Aguado, Michela Ribersani, Ramón Arroyo-Espliguero, Vicente Estrada, Lucia De Franceschi, Maurizio Miano, Antonella Massa, Alessandra Quota, Vincenzo Voi, Monica Fortini, Maria Domenica Cappellini, Inmaculada Fernández-Rozas, Marco Marziali, Giovanna Graziadei, Angelantonio Vitucci, Alberto Piperno, Iván Núñez Gil Md, Irene Motta, Wulandewi Marhaeni, Marco Zecca, Maddalena Casale, Antonio Piga, Silverio Perrotta, Bryan Rupinski, Charbel Maroun, Filomena Longo, Rodolfo Romero, R. Mariani, Domenico Roberti, Susanna Barella, Andrea Beccaria, Valeria Pinto, Barbara Gianesin, Mohammad Abumayyaleh, Rosamaria Rosso, Carolina Espejo Paeres, Álvaro Aparisi, Gian Luca Forni, Rita Gamberini, Ibrahim Akin, Anna Rita Denotti, Federico Bonetti, Alessia Marcon
Publikováno v:
SSRN Electronic Journal.
Background: Although numerous patient specific co-factors have been shown to be associated with worse outcomes in COVID-19, the prognostic value of thalasemic syndromes in COVID-19 patients remains poorly understood. Aims: We studied the outcomes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a288b2670a771cbcfbedc2dc80a2dbd
https://doi.org/10.2139/ssrn.3801721
https://doi.org/10.2139/ssrn.3801721
Autor:
Alessia, Pepe, Antonella, Meloni, Aldo, Filosa, Laura, Pistoia, Zelia, Borsellino, Domenico Giuseppe, D'Ascola, Roberto, Lisi, Maria Caterina, Putti, Massimo, Allò, Maria Rita, Gamberini, Antonella, Quarta, Carmelo, Fidone, Tommaso, Casini, Gennaro, Restaino, Massimo, Midiri, Maurizio, Mangione, Vincenzo, Positano, Maddalena, Casale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::34b6f7130b1d41b7e0b26b73aaaa4ee9
http://hdl.handle.net/11591/429172
http://hdl.handle.net/11591/429172
Autor:
Valeria Pinto, Vincenzo Voi, Barbara Gianesin, Paola Corti, Maddalena Casale, Sabrina Quintino, Gian Luca Forni, Carmelo Fidone
Manual erythroexchange (MEEX) was proven to be effective and safe in the management of sickle cell disease (SCD). The goal is to quickly reduce the percentage of hemoglobin S (HbS%). A national survey of the Italian Society for Thalassemia and Hemogl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e7f23beff34779c29c201685658faed
http://hdl.handle.net/11591/435262
http://hdl.handle.net/11591/435262
Autor:
Francesca Ferrara, Carmelo Fidone, Giovanna Graziadei, Aurelio Maggio, Maria Domenica Cappellini, Antonio Piga, Vincenzo Voi, Giovan Battista Ruffo, Laura Sainati, Lucia De Franceschi, Antonello Pietrangelo, Alessandra Quota, Maddalena Casale, Raffaella Colombatti, Valeria Pinto, Donatella Venturelli, Silverio Perrotta, Sorrentino F, Paolo Rigano, Gian Luca Forni, Giovanna Russo, Giovanni Palazzi
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS). Clinical manifestations of SCD are mainly characterized by chronic hemolysis and acute vaso-occlusive c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c18e501f553ec019298ce67aa4aa12f
http://hdl.handle.net/11591/417409
http://hdl.handle.net/11591/417409