Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Valentina, Arcangeli"'
Autor:
Giovanni Innella, Cristina Fortuno, Laura Caleca, Bing‐Jian Feng, Courtney Carroll, Michael T. Parsons, Sara Miccoli, Marco Montagna, Daniele Calistri, Laura Cortesi, Barbara Pasini, Siranoush Manoukian, Daniela Giachino, Laura Matricardi, Maria Cristina Foti, Valentina Zampiga, Claudia Piombino, Elena Barbieri, Francesca Vignolo Lutati, Jacopo Azzolini, Rita Danesi, Valentina Arcangeli, Sandrine M. Caputo, Nadia Boutry‐Kryza, Vincent Goussot, Susan Hiraki, Marcy Richardson, Hereditary Breast/Ovarian Cancer IOV network (HBOC IOVnet), Simona Ferrari, Paolo Radice, Amanda B. Spurdle, Daniela Turchetti
Publikováno v:
Cancer Medicine, Vol 13, Iss 16, Pp n/a-n/a (2024)
Abstract Background BRCA1:c.5017_5019del (p.His1673del) is a founder variant relatively frequent in Northern Italy. Despite previous suggestion of pathogenicity, variant classification in public databases is still conflicting, needing additional evid
Externí odkaz:
https://doaj.org/article/32f976e151b24f91bbf40981195926b1
Autor:
Laura Monti, Georgios D. Kotzalidis, Valentina Arcangeli, Camilla Brozzi, Rossella Iacovino, Cristina Giansanti, Daniela Belella, Elisa Marconi, Silvia Maria Pulitanò, Marianna Mazza, Giuseppe Marano, Giorgio Conti, Delfina Janiri, Gabriele Sani, Daniela Pia Rosaria Chieffo
Publikováno v:
Children, Vol 11, Iss 10, p 1218 (2024)
Background/Objectives: Although rare in the Western world, dog bites may be lethal or lead to physically severe outcomes. However, little attention is given to their psychological consequences. We aimed to review their psychological consequences in c
Externí odkaz:
https://doaj.org/article/f838593550074f129da97cfcdd9c6507
Autor:
Stefano Ferretti, Priscilla Sassoli de Bianchi, Debora Canuti, Cinzia Campari, Laura Cortesi, Valentina Arcangeli, Elena Barbieri, Cecilia D’Aloia, Rita Danesi, Pierandrea De Iaco, Margherita De Lillo, Laura Lombardo, Gabriella Moretti, Antonino Musolino, Dante Palli, Caterina Palmonari, Mila Ravegnani, Alfredo Tafà, Alessandra Tononi, Daniela Turchetti, Claudio Zamagni, Valentina Zampiga, Lauro Bucchi, the HBOC Study Group
Publikováno v:
Methods and Protocols, Vol 7, Iss 4, p 63 (2024)
Hereditary breast/ovarian cancer (HBOC) syndrome is caused by the inheritance of monoallelic germline BRCA1/2 gene mutations. If BRCA1/2 mutation carriers are identified before the disease develops, effective actions against HBOC can be taken, includ
Externí odkaz:
https://doaj.org/article/45a7886160724011a27d7da7efcaef86
Autor:
Alberto Farolfi, Elisabetta Petracci, Giorgia Gurioli, Gianluca Tedaldi, Claudia Casanova, Valentina Arcangeli, Andrea Amadori, Marta Rosati, Marco Stefanetti, Salvatore Luca Burgio, Maria Concetta Cursano, Cristian Lolli, Valentina Zampiga, Ilaria Cangini, Giuseppe Schepisi, Ugo De Giorgi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionPrimary debulking surgery (PDS), interval debulking surgery (IDS), and platinum-based chemotherapy are the current standard treatments for advanced ovarian cancer (OC). The time to initiation of adjuvant chemotherapy (TTC) could influence
Externí odkaz:
https://doaj.org/article/81e7da35c11248dd81c0be1df7cd92e2
Autor:
Fabrizio Cocciolillo, Daniela Pia Rosaria Chieffo, Alessandro Giordano, Valentina Arcangeli, Ilaria Lazzareschi, Rosa Morello, Giuseppe Zampino, Piero Valentini, Danilo Buonsenso
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundLong coronavirus disease (COVID) is increasingly recognized in adults and children; however, it is still poorly characterized from a clinical and diagnostic perspective, particularly in the younger populations.Case presentationWe described
Externí odkaz:
https://doaj.org/article/cc7c6796ae85469bae80bc85aac76314
Autor:
Valentina Massaroni, Valentina Delle Donne, Camillo Marra, Valentina Arcangeli, Daniela Pia Rosaria Chieffo
Publikováno v:
Brain Sciences, Vol 14, Iss 1, p 27 (2023)
Screen time refers to the amount of time a child is exposed to a screen, that is, television, computer, smartphone, or any other digital medium. Prolonged screen time in the first years of life may affect a child’s cognitive abilities, especially l
Externí odkaz:
https://doaj.org/article/ae8c4f6ec766489a8f98b323c10d94ec
Autor:
Daniela Pia Rosaria Chieffo, Valentina Arcangeli, Federica Moriconi, Angelica Marfoli, Federica Lino, Sofia Vannuccini, Elisa Marconi, Ida Turrini, Claudia Brogna, Chiara Veredice, Alessandro Antonietti, Gabriele Sani, Eugenio Maria Mercuri
Publikováno v:
Children, Vol 10, Iss 8, p 1356 (2023)
Introduction: Specific Learning Disorder (SLD) is a neurodevelopmental disorder characterized by difficulties in perceiving and processing verbal and non-verbal information. It is usually accompanied by impaired academic skills leading to school drop
Externí odkaz:
https://doaj.org/article/2857525cee714ce0be301c89e0be1f26
Autor:
Ilario Giovanni Rapposelli, Valentina Zampiga, Ilaria Cangini, Valentina Arcangeli, Mila Ravegnani, Martina Valgiusti, Sara Pini, Stefano Tamberi, Giulia Bartolini, Alessandro Passardi, Giovanni Martinelli, Daniele Calistri, Giovanni Luca Frassineti, Fabio Falcini, Rita Danesi
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background Pancreatic cancer (PC) is a major cause of cancer death. In an effort to improve treatment strategies and outcomes, DNA damage repair (DDR) pathways have been introduced as a new target in PC and in other cancers, through the expl
Externí odkaz:
https://doaj.org/article/eb588727dceb41739f721cc956da76f5
Publikováno v:
Korean Journal of Anesthesiology, Vol 74, Iss 6, Pp 552-554 (2021)
Externí odkaz:
https://doaj.org/article/2c35853ee46e4db98d7575d880d7ddc5
Autor:
Erika Bandini, Ilaria Cangini, Valentina Arcangeli, Mila Ravegnani, Virginia Andreotti, Giovanna Prisinzano, Lorenza Pastorino, Giovanni Martinelli, Fabio Falcini, Daniele Calistri, Valentina Zampiga, Rita Danesi
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Birt–Hogg–Dubé syndrome (BHDS) is a rare autosomal dominant inherited disorder caused by a mutation in folliculin (FLCN) gene transmitted via germline autosomal dominant pattern. Patients with this syndrome have an increased susceptibility to re
Externí odkaz:
https://doaj.org/article/1d148c0101d04f9e91aece46a508a586