Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Antonella Cacchione"'
Autor:
Giada Del Baldo, Angela Mastronuzzi, Selene Cipri, Emanuele Agolini, Marta Matraxia, Antonio Novelli, Antonella Cacchione, Annalisa Serra, Andrea Carai, Luigi Boccuto, Giovanna Stefania Colafati, Pier Luigi Di Paolo, Evelina Miele, Sabina Barresi, Rita Alaggio, Sabrina Rossi, Isabella Giovannoni
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Cancer predisposition syndromes are recognized in about 10% of pediatric malignancies with several genes specifically involved in a subset of pediatric tumors such as DICER1, in pleuropulmonary blastoma, cystic nephroma, and brain sarcomas.
Externí odkaz:
https://doaj.org/article/6e9544ccf65a442488bd95429b65a943
Autor:
Sara Patrizi, Evelina Miele, Lorenza Falcone, Silvia Vallese, Sabrina Rossi, Sabina Barresi, Isabella Giovannoni, Lucia Pedace, Claudia Nardini, Ilaria Masier, Luana Abballe, Antonella Cacchione, Ida Russo, Angela Di Giannatale, Valentina Di Ruscio, Claudia Maria Salgado, Angela Mastronuzzi, Andrea Ciolfi, Marco Tartaglia, Giuseppe Maria Milano, Franco Locatelli, Rita Alaggio
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-12 (2024)
Abstract Background Malignant peripheral nerve sheath tumors (MPNSTs) account for 3–10% of pediatric sarcomas, 50% of which occur in neurofibromatosis type 1 (NF1). Sporadic MPNSTs diagnosis may be challenging due to the absence of specific markers
Externí odkaz:
https://doaj.org/article/e153def98c9c43fea6e3e57bc6160250
Autor:
Ioan Paul Voicu, Francesco Dotta, Antonio Napolitano, Massimo Caulo, Eleonora Piccirilli, Claudia D’Orazio, Andrea Carai, Evelina Miele, Maria Vinci, Sabrina Rossi, Antonella Cacchione, Sabina Vennarini, Giada Del Baldo, Angela Mastronuzzi, Paolo Tomà, Giovanna Stefania Colafati
Publikováno v:
Cancers, Vol 16, Iss 14, p 2578 (2024)
Background and purpose: Differentiating pediatric posterior fossa (PF) tumors such as medulloblastoma (MB), ependymoma (EP), and pilocytic astrocytoma (PA) remains relevant, because of important treatment and prognostic implications. Diffusion kurtos
Externí odkaz:
https://doaj.org/article/b6a82dd574f24d7b8aa067628f866b49
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Externí odkaz:
https://doaj.org/article/4b0d5e903c874fcfb84e86d5aa5f00c6
Autor:
Federica D’Antonio, Sabrina Rossi, Isabella Giovannoni, Rita Alaggio, Andrea Carai, Giuseppe M. Milano, Antonella Cacchione, Alessandra Cancellieri, Marco Gessi, Manila Antonelli, Giovanna S. Colafati, Giacomina Megaro, Sabina Vennarini, Angela Mastronuzzi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundIntracranial mesenchymal tumors are a rare type of neoplasm (0.3% of all soft tissue tumors) characterized by a fusion of a FET family gene (usually EWSR1, rarely FUS) to CREB family genes (CREB1, ATF1, and CREM) with a slow-growing and fav
Externí odkaz:
https://doaj.org/article/eecde83982b8444d992cf20a06cedd79
Autor:
Giada Del Baldo, Sabina Vennarini, Maristella Toniutti, Rachid Abbas, Stefano Lorentini, Eleonora Piccirilli, Antonella Cacchione, Giacomina Megaro, Valentina Di Ruscio, Maria Antonietta De Ioris, Andrea De Salvo, Giulia Albino, Sabrina Rossi, Giovanna Stefania Colafati, Andrea Carai, Angela Mastronuzzi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundGerm cell tumors (GCT) account for a minority of central nervous system (CNS) malignancies, highly prevalent in adolescents and young adults. Despite their aggressive biological behavior, prognosis is excellent in most cases with risk strat
Externí odkaz:
https://doaj.org/article/5931247dd8ba44e0a7f045301eb3538d
Autor:
Anna Maria Caroleo, Silvia Rotulo, Emanuele Agolini, Marina Macchiaiolo, Luigi Boccuto, Manila Antonelli, Giovanna Stefania Colafati, Antonella Cacchione, Giacomina Megaro, Andrea Carai, Maria Antonietta De Ioris, Mariachiara Lodi, Assunta Tornesello, Valeria Simone, Filippo Torroni, Giuseppe Cinalli, Angela Mastronuzzi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) is a cancer predisposition syndrome characterized by an increased risk of developing benign and malignant tumors, caused by germline pathogenic variants of the PTEN tumour suppress
Externí odkaz:
https://doaj.org/article/503a38aa24fe4b618452fafd6c80ad26
Autor:
Lucia De Martino, Stefania Picariello, Carmela Russo, Maria Elena Errico, Pietro Spennato, Maria Rosaria Papa, Nicola Normanno, Giuseppe Scimone, Giovanna Stefania Colafati, Antonella Cacchione, Angela Mastronuzzi, Maura Massimino, Giuseppe Cinalli, Lucia Quaglietta
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
IntroductionPediatric diffuse midline gliomas (DMG), H3 K27- altered, are the most aggressive pediatric central nervous system (CNS) malignancies. Disease outcome is dismal with a median survival of less than one year. Extra-neural metastases are an
Externí odkaz:
https://doaj.org/article/be6ab18d997c4ffd985367185bd753e8
Autor:
Giuseppina Catanzaro, Zein Mersini Besharat, Andrea Carai, Natalie Jäger, Elena Splendiani, Carole Colin, Agnese Po, Martina Chiacchiarini, Anna Citarella, Francesca Gianno, Antonella Cacchione, Evelina Miele, Francesca Diomedi Camassei, Marco Gessi, Luca Massimi, Franco Locatelli, David T. W. Jones, Dominique Figarella-Branger, Stefan M. Pfister, Angela Mastronuzzi, Felice Giangaspero, Elisabetta Ferretti
Publikováno v:
Biomarker Research, Vol 10, Iss 1, Pp 1-17 (2022)
Abstract Background Pediatric low-grade gliomas (pLGGs), particularly incompletely resected supratentorial tumours, can undergo progression after surgery. However to date, there are no predictive biomarkers for progression. Here, we aimed to identify
Externí odkaz:
https://doaj.org/article/69244695ff9e49f0b2da857c1dfb8362
Autor:
Giada Del Baldo, Francesca Del Bufalo, Claudia Pinacchio, Andrea Carai, Concetta Quintarelli, Biagio De Angelis, Pietro Merli, Antonella Cacchione, Franco Locatelli, Angela Mastronuzzi
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Childhood malignant brain tumors remain a significant cause of death in the pediatric population, despite the use of aggressive multimodal treatments. New therapeutic approaches are urgently needed for these patients in order to improve prognosis, wh
Externí odkaz:
https://doaj.org/article/4dd8274939b54ffea9f0c941d210bd49