Zobrazeno 1 - 10
of 742
pro vyhledávání: '"Francesco, Fabozzi"'
Publikováno v:
Frontiers in Nutrition, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/cbff964cfc424ba78542d31d3cca1b51
Autor:
Maria Antonietta De Ioris, Francesco Fabozzi, Francesca Del Bufalo, Giada Del Baldo, Maria Felicia Villani, Maria Giuseppina Cefalo, Maria Carmen Garganese, Alessandra Stracuzzi, Federica Tangari, Arturo Maria Greco, Isabella Giovannoni, Roberto Carta, Maria Luisa D’Andrea, Angela Mastronuzzi, Franco Locatelli
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-5 (2023)
Abstract The prognosis of relapsed/refractory (R/R) neuroblastoma (NB) is dismal, calling for new therapeutic strategies. Venetoclax (VEN) is a highly selective, potent, orally bioavailable, BCL-2 inhibitor small-molecule that showed a synergistic ef
Externí odkaz:
https://doaj.org/article/d9a3f4ab567b4cb2b052b48621dda13d
Autor:
Francesco Fabozzi, Rosalba Carrozzo, Mariachiara Lodi, Angela Di Giannatale, Selene Cipri, Chiara Rosignoli, Isabella Giovannoni, Alessandra Stracuzzi, Teresa Rizza, Claudio Montante, Emanuele Agolini, Michela Di Nottia, Federica Galaverna, Giada Del Baldo, Francesco Del Bufalo, Angela Mastronuzzi, Maria Antonietta De Ioris
Publikováno v:
Frontiers in Oncology, Vol 13 (2024)
The increased availability of genetic technologies has significantly improved the detection of novel germline variants conferring a predisposition to tumor development in patients with malignant disease. The identification of variants of uncertain si
Externí odkaz:
https://doaj.org/article/9a9082b1342045729d45a563947a18ad
Autor:
Selene Cipri, Francesco Fabozzi, Giada Del Baldo, Giuseppe Maria Milano, Luigi Boccuto, Andrea Carai, Angela Mastronuzzi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
The family of the neurotrophic tyrosine kinase receptor (NTRK) gene encodes for members of the tropomyosin receptor kinase (TRK) family. Rearrangements involving NTRK1/2/3 are rare oncogenic factors reported with variable frequencies in an extensive
Externí odkaz:
https://doaj.org/article/cf10beb382ba46aeafc72aef2a0d4839
Autor:
Alberto Eugenio Tozzi, Ileana Croci, Paul Voicu, Francesco Dotta, Giovanna Stefania Colafati, Andrea Carai, Francesco Fabozzi, Giuseppe Lacanna, Roberto Premuselli, Angela Mastronuzzi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionEurope works to improve cancer management through the use of artificialintelligence (AI), and there is a need to accelerate the development of AI applications for childhood cancer. However, the current strategies used for algorithm develo
Externí odkaz:
https://doaj.org/article/3576878600004d74b2062c7bdbc5fb54
Autor:
Selene Cipri, Giada Del Baldo, Francesco Fabozzi, Luigi Boccuto, Andrea Carai, Angela Mastronuzzi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
In the past decade significant advancements have been made in the discovery of targetable lesions in pediatric low-grade gliomas (pLGGs). These tumors account for 30-50% of all pediatric brain tumors with generally a favorable prognosis. The latest 2
Externí odkaz:
https://doaj.org/article/d55253fed96e488195cf82a47ad3b1ef
Autor:
Francesco Sciancalepore, Francesco Fabozzi, Giulia Albino, Giada Del Baldo, Valentina Di Ruscio, Beatrice Laus, Danilo Menegatti, Roberto Premuselli, Domitilla Elena Secco, Alberto Eugenio Tozzi, Eleonora Lacorte, Nicola Vanacore, Andrea Carai, Angela Mastronuzzi, Allena-Mente Study Group
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundThis systematic review has been conducted with the aim of characterizing cognitive deficits and analyzing their frequency in survivors of paediatric Central Nervous System tumours.Materials and methodsAll literature published up to January
Externí odkaz:
https://doaj.org/article/581c78f08ce94e79a6203365b9cee287
Autor:
Francesco Fabozzi, Angela Mastronuzzi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Advances in molecular biology and genetic testing have greatly improved our understanding of the genetic basis of hematologic malignancies and have enabled the identification of new cancer predisposition syndromes. The recognition of a germline mutat
Externí odkaz:
https://doaj.org/article/d490e3178a274704aef7df54594080b3
Autor:
Antonella Cacchione MD, Francesco Fabozzi MD, Andrea Carai MD, PhD, Giovanna Stefania Colafati MD, Giada del Baldo MD, Sabrina Rossi MD, Martino Diana MD, Giacomina Megaro MD, Giuseppe Maria Milano MD, PhD, Marina Macchiaiolo MD, Alessandro Crocoli MD, Maria Antonietta De Ioris MD, Luigi Boccuto MD, Domitilla Elena Secco MD, Mario Zama MD, Emanuele Agolini MD, Paolo Tomà, Angela Mastronuzzi MD, PhD
Publikováno v:
Cancer Control, Vol 30 (2023)
Introduction Plexiform neurofibromas (PN) represent the main cause of morbidity in patients affected by Neurofibromatosis Type 1 (NF1). Until recently, surgery has been the main treatment option in these patients, but it is burdened with a low effica
Externí odkaz:
https://doaj.org/article/c71c0bb345cb455e834e23068b4708cd
Autor:
Francesco Fabozzi, Rita De Vito, Stefania Gaspari, Fabrizio Leone, Maurizio Delvecchio, Emanuele Agolini, Federica Galaverna, Angela Mastronuzzi, Daria Pagliara, Maria Antonietta De Ioris
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
We reported a new pathogenic variant of LRBA deficiency with a complex phenotype—neonatal diabetes, very early-onset inflammatory bowel disease, and polyarthritis—who presented with lymph node enlargement. A case of Rosai-Dorfman’s disease (RDD
Externí odkaz:
https://doaj.org/article/545da8a76a5b426199371beba67b5b76