Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Giovanna Mangili"'
Autor:
Lorenza Pugni, Beatrice Letizia Crippa, Francesco Raimondi, Giovanni Vento, Giovanna Mangili, Alessandra Coscia, Giacomo Artieri, Andrea Ronchi, Maria Luisa Ventura, Paola Lago, Carlo Pietrasanta, Riccardo Crimi, Giuseppina Bonfante, Serafina Perrone, Alessandra Boncompagni, Agostina Solinas, Massimo Agosti, Chiara Poggi, Alessandra Falcone, Claudia Pagliotta, Daniela Gianotti, Genny Gottardi, Giulia Paviotti, Alessandra Allodi, Gianfranco Maffei, Alice Proto, Antonella Travierso, Serena Salomè, Simonetta Costa, Stefania Ferrari, Chiara Peila, Mariateresa Sinelli, Federica Fanelli, Lucia Giordano, Martina Saruggia, Letizia Capasso, Elena Spada, Camilla Gizzi, Luigi Orfeo, Fabio Mosca
Publikováno v:
International Journal of Infectious Diseases, Vol 140, Iss , Pp 17-24 (2024)
Objectives: To describe how SARS-CoV-2 infection at the time of delivery affected maternal and neonatal outcomes across four major waves of the COVID-19 pandemic in Italy. Methods: This is a large, prospective, nationwide cohort study collecting mate
Externí odkaz:
https://doaj.org/article/a253eadf2ac24f0990fb00a4bb4082a7
Autor:
Lidia Pezzani, Laura Pezzoli, Alessandra Pansa, Barbara Facchinetti, Daniela Marchetti, Agnese Scatigno, Anna R. Lincesso, Loredana Perego, Monica Pingue, Isabella Pellicioli, Lucia Migliazza, Giovanna Mangili, Lorenzo Galletti, Ursula Giussani, Ezio Bonanomi, Anna Cereda, Maria Iascone
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background In the last few years trio‐whole exome sequencing (WES) analysis has demonstrated its potential in obtaining genetic diagnoses even in nonspecific clinical pictures and in atypical presentations of known diseases. Moreover WES a
Externí odkaz:
https://doaj.org/article/37960e69999c427d889309a579225219
Autor:
Laura Pezzoli, Lidia Pezzani, Ezio Bonanomi, Chiara Marrone, Agnese Scatigno, Anna Cereda, Maria Francesca Bedeschi, Angelo Selicorni, Serena Gasperini, Paolo Bini, Silvia Maitz, Carla Maccioni, Cristina Pedron, Lorenzo Colombo, Daniela Marchetti, Matteo Bellini, Anna Rita Lincesso, Loredana Perego, Monica Pingue, Nunzia Della Malva, Giovanna Mangili, Paolo Ferrazzi, Maria Iascone
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 1, p 2 (2021)
Whole-exome sequencing (WES) is a powerful and comprehensive tool for the genetic diagnosis of rare diseases, but few reports describe its timely application and clinical impact on infantile cardiomyopathies (CM). We conducted a retrospective analysi
Externí odkaz:
https://doaj.org/article/3c235ef6734140edb0e00c0d4af8ab5b
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 40, Iss 1 (2018)
Congenital heart disease (CHD) is the most common neonatal congenital malformation. The variety and severity of clinical presentation depend on the cardiac structures involved and their functional impact. The management of newborns with CHD requires
Externí odkaz:
https://doaj.org/article/8e695d10835e4925998ff90cbb42d4cf
Autor:
Giovanna Mangili, Elena Garzoli
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 39, Iss 2 (2017)
The administration of the adequate amount of nutrients helps to improve a correct short-term linear growth and long-term neurocognitive development. To reduce the extra-uterine growth delay in very low birth weight infants (VLBW) the best strategy of
Externí odkaz:
https://doaj.org/article/095886ed170947ddab4b899e4a0786d3
Autor:
Lara Cirnigliaro, Paolo Bianchi, Luisa Sturiale, Domenico Garozzo, Giovanna Mangili, Liesbeth Keldermans, Renata Rizzo, Gert Matthijs, Agata Fiumara, Jaak Jaeken, Rita Barone
BACKGROUND: Deficiency of Conserved Oligomeric Golgi (COG) subunits (COG1-8) is characterized by both N- and O-protein glycosylation defects associated with destabilization and mislocalization of Golgi glycosylation machinery components (COG-CDG). Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774acb3fc2a20adbaa5a275b0e6e0108
http://hdl.handle.net/20.500.11769/519377
http://hdl.handle.net/20.500.11769/519377
Autor:
Lorenzo D'Antiga, Marina Pace, Maurizio Cheli, Sandro Sironi, Antonino Barletta, Giovanna Mangili
Publikováno v:
Clinical Imaging. 54:25-30
Omphalopagus twins are joined ventrally in the umbilical region. In omphalopagus twins, liver's fusion is very frequent, being present in about 80% of cases. Two conjoined twins born in our Hospital were evaluated using plain x-rays, ultrasound (US),
Autor:
Ezio Bonanomi, Maria Iascone, Lorenzo Galletti, Monica Pingue, Alessandra Pansa, Giovanna Mangili, Lucia Migliazza, Daniela Marchetti, Barbara Facchinetti, Anna Cereda, Lidia Pezzani, Anna R. Lincesso, Ursula Giussani, Isabella Pellicioli, Agnese Scatigno, Laura Pezzoli, Loredana Perego
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Background In the last few years trio‐whole exome sequencing (WES) analysis has demonstrated its potential in obtaining genetic diagnoses even in nonspecific clinical pictures and in atypical presentations of known diseases. Moreover WES allows the
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 40, Iss 1 (2018)
Congenital heart disease (CHD) is the most common neonatal congenital malformation. The variety and severity of clinical presentation depend on the cardiac structures involved and their functional impact. The management of newborns with CHD requires
Autor:
Mario, Mastrangelo, Filippo, Manti, Luisa, Patanè, Stefania, Ferrari, Carla, Carducci, Claudia, Carducci, Giovanna, Mangili, Vincenzo, Leuzzi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2053fdd433b939593a14dd1b94de97d4
http://hdl.handle.net/11573/1143252
http://hdl.handle.net/11573/1143252