Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Attilio, Rovelli"'
Autor:
Alessandro Cattoni, Sofia Chiaraluce, Serena Gasperini, Silvia Molinari, Andrea Biondi, Attilio Rovelli, Rossella Parini
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss , Pp 100787- (2021)
The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mucopolysaccharidosis I Hurler (MPS-IH) has been historically regarded as unsatisfactory. Nevertheless, the growth patterns recorded in transplanted pat
Externí odkaz:
https://doaj.org/article/871bed4ef1294b12b94b5522a97289e9
Autor:
Anna Maria Peri, Marta Verna, Stefano Biffi, Laura Alagna, Benedetta Longhi, Guglielmo Marco Migliorino, Sergio Foresti, Alessandra Bandera, Attilio Rovelli, Carmelo Rizzari, Andrea Gori, Antonella Colombini
Publikováno v:
Pathogens and Immunity, Vol 4, Iss 2, Pp 180-194 (2019)
Background: Invasive mold infections in children with hematological malignancies are associated with high mortality rates. The use of combination antifungal therapy in cases with a severe clinical course is increasing, although information on the eff
Externí odkaz:
https://doaj.org/article/91dc5f12cd7e47cda616ff4f53c9fa8f
Autor:
Francesca Furlan, Attilio Rovelli, Miriam Rigoldi, Mirella Filocamo, Barbara Tappino, Douglas Friday, Serena Gasperini, Silvana Mariani, Claudia Izzi, Maria Pia Bondioni, Cinzia Gellera, Anna Venerando, Nicoletta Villa, Maria del Carmen Rodriguez Perez, Fabio Pavan, Andrea Biondi, Rossella Parini
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss S2, Pp 155-161 (2018)
Abstract A new patient with severe mucopolysaccharidosis (MPS) type VII is reported. Non-immune hydrops fetalis (NIHF) was diagnosed during pregnancy. At birth, he showed generalized hydrops and dysmorphic features typical of MPS. Many diagnoses were
Externí odkaz:
https://doaj.org/article/bf196ba6282642fb95ff385ad35b564e
Autor:
Silvia Nucera, Grazia Fazio, Rocco Piazza, Silvia Rigamonti, Diletta Fontana, Carlo Gambacorti Passerini, Silvia Maitz, Attilio Rovelli, Andrea Biondi, Giovauni Cazzaniga, Adriana Balduzzi
Publikováno v:
HemaSphere, Vol 4, Iss 5, p e460 (2020)
Externí odkaz:
https://doaj.org/article/f25f4da871414192bc7e6648d2da6d26
Autor:
Guido Costamagna, MD, FACG, FJGES, Vincenzo Bove, MD, Antonio Ruggiero, MD, Attilio Rovelli, MD, Andrea Tringali, MD, PhD
Publikováno v:
VideoGIE, Vol 6, Iss 4, Pp 176-177 (2021)
Externí odkaz:
https://doaj.org/article/10f41bd7ab9149bea0f51170c2629ee0
Autor:
Ignazio Majolino, Dereen Mohammed, Dastan Hassan, Francesco Ipsevich, Chra Abdullah, Rebar Mohammed, Angelo Palmas, Marco Possenti, Diana Noori, Dlir Ali, Harem Karem, Salah Salih, Michele Vacca, Claudia Del Fante, Angelo Ostuni, Andrea Frigato, Maria Speranza Massei, Annunziata Manna, Stefania Vasta, Marcela Gabriel, Marta Verna, Attilio Rovelli, Valentino Conter, Kosar Ali, Dosti Othman
Publikováno v:
Journal of Global Oncology, Vol 4, Pp 1-8 (2017)
Introduction: At Hiwa Cancer Hospital (Sulaymaniyah, Iraqi Kurdistan) after the center was started by a cooperative project in June 2016, autologous transplantation was developed. Patients and Methods: To develop the project, the capacity-building ap
Externí odkaz:
https://doaj.org/article/6205ba151248437980c4a45e5a59459e
Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
Autor:
Mieke Aldenhoven, Brigitte T.A. van den Broek, Robert F. Wynn, Anne O'Meara, Paul Veys, Attilio Rovelli, Simon A. Jones, Rossella Parini, Peter M. van Hasselt, Marleen Renard, Victoria Bordon, Tom J. de Koning, Jaap Jan Boelens
Publikováno v:
Blood Advances, Vol 1, Iss 24, Pp 2236-2242 (2017)
Abstract: Hurler syndrome (HS) is a lysosomal storage disease characterized by multisystem morbidity and death in early childhood. Hematopoietic stem cell transplantation (HSCT) results in long-term survival, although with significant residual diseas
Externí odkaz:
https://doaj.org/article/816b9f5cde4c46069c9a97066048c833
Autor:
Rossella Parini, Federica Deodato, Maja Di Rocco, Edoardo Lanino, Franco Locatelli, Chiara Messina, Attilio Rovelli, Maurizio Scarpa
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-9 (2017)
Abstract Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic disease caused by mutations of IDUA gene encoding the lysosomal α-L-iduronidase enzyme. MPS I-H is a rare, life-threatening disease, evolving in multisy
Externí odkaz:
https://doaj.org/article/cfa741142ece4f568cd344f804fa569f
Autor:
Bernhard, Gentner, Francesca, Tucci, Stefania, Galimberti, Francesca, Fumagalli, Maurizio, De Pellegrin, Paolo, Silvani, Chiara, Camesasca, Silvia, Pontesilli, Silvia, Darin, Francesca, Ciotti, Marina, Sarzana, Giulia, Consiglieri, Chiara, Filisetti, Giulia, Forni, Laura, Passerini, Daniela, Tomasoni, Daniela, Cesana, Andrea, Calabria, Giulio, Spinozzi, Maria-Pia, Cicalese, Valeria, Calbi, Maddalena, Migliavacca, Federica, Barzaghi, Francesca, Ferrua, Vera, Gallo, Simona, Miglietta, Erika, Zonari, Patali S, Cheruku, Claudia, Forni, Marcella, Facchini, Ambra, Corti, Michela, Gabaldo, Stefano, Zancan, Serena, Gasperini, Attilio, Rovelli, Jaap-Jan, Boelens, Simon A, Jones, Robert, Wynn, Cristina, Baldoli, Eugenio, Montini, Silvia, Gregori, Fabio, Ciceri, Maria G, Valsecchi, Giancarlo, la Marca, Rossella, Parini, Luigi, Naldini, Alessandro, Aiuti, Maria-Ester, Bernardo, Ilaria, Visagalli
Publikováno v:
New England Journal of Medicine. 385:1929-1940
Background Allogeneic hematopoietic stem-cell transplantation is the standard of care for Hurler syndrome (mucopolysaccharidosis type I, Hurler variant [MPSIH]). However, this treatment is only partially curative and is associated with complications.
Autor:
Sonia Bonanomi, Andrea Biondi, Laura Rachele Bettini, Giorgio Ottaviano, Roberto Rona, Sara Napolitano, Adriana Balduzzi, Attilio Rovelli, Vincenzo Russotto
Publikováno v:
Tumori Journal. 108:556-562
Background: Cytokine release syndrome (CRS) is a major complication after chimeric-antigen receptor T-cell treatment, characterized by an uncontrolled systemic inflammatory reaction. We investigated the potential role of diclofenac in the management