Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Tommaso Mina"'
Autor:
Raffaele Mattera, Maria Caterina Putti, Alessandra Biffi, Rosanna Parasole, Valentino Conter, Carmelo Rizzari, Maria Grazia Valsecchi, Daniela Silvestri, Andrea Biondi, Franco Locatelli, Elena Barisone, Concetta Micalizzi, Tommaso Mina, Valentina Kiren
Publikováno v:
HemaSphere, Vol 7, p e1005163 (2023)
Externí odkaz:
https://doaj.org/article/ff021e86dbe64d45ace6d546216fc8bf
Autor:
Pietro Merli, Daria Pagliara, Tommaso Mina, Valentina Bertaina, Giuseppina Li Pira, Stefania Lazzaro, Simone Biagini, Federica Galaverna, Luisa Strocchio, Roberto Carta, Maria Luigia Catanoso, Francesco Quagliarella, Marco Becilli, Emilia Boccieri, Francesca Del Bufalo, Arianna Panigari, Annalisa Agostini, Lucia Pedace, Simone Pizzi, Cesare Perotti, Mattia Algeri, Marco Zecca, Franco Locatelli
Publikováno v:
Haematologica, Vol 107, Iss 12 (2022)
Externí odkaz:
https://doaj.org/article/0dd6b69d88bb495aad7ddaebc370a058
Autor:
Andrea Santangelo, Emanuele Bartolini, Giulia Nuzzi, Thomas Foiadelli, Alexandre Michev, Tommaso Mina, Irene Trambusti, Valeria Fichera, Alice Bonuccelli, Gabriele Massimetti, Diego G. Peroni, Emanuela De Marco, Luca Coccoli, Laura Luti, Sayla Bernasconi, Margherita Nardi, Maria Cristina Menconi, Gabriella Casazza, Dario Pruna, Rosamaria Mura, Chiara Marra, Daniele Zama, Pasquale Striano, Duccio M. Cordelli, Roberta Battini, Alessandro Orsini
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionStroke-like syndrome (SLS) is a rare subacute neurological complication of intrathecal or high-dose (≥500 mg) Methotrexate (MTX) administration. Its clinical features, evoking acute cerebral ischaemia with fluctuating course symptoms an
Externí odkaz:
https://doaj.org/article/3fb8b8378d5a47a782bcc6546e9e5fd0
Autor:
Francesca Compagno, Sabrina Basso, Arianna Panigari, Jessica Bagnarino, Luca Stoppini, Alessandra Maiello, Tommaso Mina, Paola Zelini, Cesare Perotti, Fausto Baldanti, Marco Zecca, Patrizia Comoli
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Post-transplant lymphoproliferative disorders (PTLDs) are life-threatening complications of iatrogenic immune impairment after allogeneic hematopoietic stem cell transplantation (HSCT). In the pediatric setting, the majority of PTLDs are related to t
Externí odkaz:
https://doaj.org/article/ccbe6f159cef40c9b6111c33bcb16ce3
Autor:
Aesha Ibrahim Khalel Ali, Darawan Rinchai, Sara Deola, Mohammed Elanbari, Dhanya Kizhakayil, Shimaa Mohammed Sherif Khedr, Mohammed Toufiq, Tommaso Mina, Kulsoom Ghias, Zehra Fadoo, Sheanna M. Herrera, Che-Ann Lachica, Blessing Dason, Anila Ejaz, Elkhansa E. Elgaali, Ayman Saleh, Davide Bedognetti, Chiara Cugno
Publikováno v:
Blood. 140:11420-11422
Autor:
Lucia Fusco, Laura Sainati, Marta Elena Santarone, Arianna Aceti, Giuseppe Milito, Davide Barbon, Chiara Iurato, Chiara Marra, Giovanni Farello, Riccardo Masetti, Tommaso Mina, Thomas Foiadelli, Francesco Toni, Stefano Sartori, Duccio Maria Cordelli, Lucio Giordano, Daniele Zama, Alessandro Orsini, Alberto Verrotti, Lara Ciampoli
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 30
Aim: The aim of this study was to describe the characteristics of Posterior Reversible Encephalopathy Syndrome (PRES) in infants and young children (
Autor:
Valentina Bertaina, Emilia Boccieri, Stefania Lazzaro, Roberto Carta, Annalisa Agostini, Francesca Del Bufalo, Mattia Algeri, Marco Zecca, Federica Galaverna, Marco Becilli, Daria Pagliara, Tommaso Mina, Pietro Merli, Luisa Strocchio, Simone Biagini, Franco Locatelli, Francesco Quagliarella, Arianna Panigari, Giuseppina Li Pira
Publikováno v:
Blood. 138:170-170
Background: Pediatric myelodysplastic syndromes (MDSs) are a heterogeneous group of clonal disorders, accounting for less than 5% of childhood hematologic malignancies. Usual indications to HSCT are: MDSs with excess of blasts, MDSs secondary to prev
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Autor:
Maria Romagnoli, Marco Zecca, Annalisa Vetro, Anita Wischmeijer, Miriam Carella, Patrizia Sacchini, Edoardo Errichiello, Tommaso Mina, Tiziana Venesio, Orsetta Zuffardi, Enrico Berrino
Publikováno v:
Blood Cells, Molecules & Diseases
Diamond-Blackfan anemia (DBA) is a rare congenital disorder presenting remarkable phenotypic overlap with other inherited bone marrow failure syndromes, making differential diagnosis challenging and its confirmation often reached with great delay. By
Autor:
Giusy Gentilcore, Ramzi Temanni, Tommaso Mina, Chiara Cugno, Muhammad Elnaggar, Fazulur R Vempalli, Sara Deola, Sheanna M Herrera, Che-Ann Lachica, Irene Cavattoni, Dhanya Kizhakayil, Zehra Fadoo, Kulsoom Ghias, Irene Pusceddu, Patrizia Comoli, Ayman Saleh, Najeeb Syed, Anila Ejaz
Publikováno v:
Blood. 136:20-21
Acute leukemias (AL) is a major cause of cancer death in young age. Extensive research is being conducted to identify novel and innovative approaches for leukemia treatment. Transcriptomic and epigenetic studies might help to discover potential targe