Zobrazeno 1 - 10
of 253
pro vyhledávání: '"Giuseppe, Zampino"'
Autor:
Valentina Trevisan, Eugenio De Corso, Germana Viscogliosi, Roberta Onesimo, Alessandro Cina, Marco Panfili, Lucrezia Perri, Cristiana Agazzi, Valentina Giorgio, Donato Rigante, Giovanni Vento, Patrizia Papacci, Filomena Valentina Paradiso, Sara Silvaroli, Lorenzo Nanni, Nicoletta Resta, Marco Castori, Jacopo Galli, Gaetano Paludetti, Giuseppe Zampino, Chiara Leoni
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Background Lymphatic malformations are vascular developmental anomalies varying from local superficial masses to diffuse infiltrating lesions, resulting in disfigurement. Patients’ outcomes range from spontaneous regression to severe seque
Externí odkaz:
https://doaj.org/article/87792ea812b04cb19a34faf827c6c476
Autor:
Anna Camporesi, Rosa Morello, Anna La Rocca, Giuseppe Zampino, Federico Vezzulli, Daniel Munblit, Francesca Raffaelli, Piero Valentini, Danilo Buonsenso
Publikováno v:
EClinicalMedicine, Vol 76, Iss , Pp 102815- (2024)
Summary: Background: Children can develop Long Covid, however long term outcomes and their predictors are poorly described in these patients. The primary aim is to describe characteristics and predictors of Long Covid in children assessed in-clinics
Externí odkaz:
https://doaj.org/article/5d6f430ddadc49e5a1a4143a591ef569
Autor:
Angela Maria Giada Giovenale, Elisa Maria Turco, Martina Mazzoni, Ilaria Ferrone, Barbara Torres, Laura Bernardini, Edvige Vulcano, Daniela Ferrari, Roberta Onesimo, Stefano D’Arrigo, Giuseppe Zampino, Maria Pennuto, Alessandro De Luca, Angelo Luigi Vescovi, Jessica Rosati
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103544- (2024)
Smith-Magenis syndrome (SMS) is a complex neurodevelopmental disorder with a birth incidence of 1:25,000. SMS is caused by haploinsufficiency of the retinoic acid-induced retinoic acid1 (RAI1) gene, determined by an interstitial deletion of ∼ 3.7 M
Externí odkaz:
https://doaj.org/article/c7d1741ad7fa4ba3a093621038ca309c
Autor:
Elisa Musto, Maria Luigia Gambardella, Marco Perulli, Michela Quintiliani, Chiara Veredice, Tommaso Verdolotti, Giovanna Berté, Chiara Leoni, Roberta Onesimo, Silvia Maria Pulitanò, Marco Tartaglia, Giuseppe Zampino, Ilaria Contaldo, Domenica Immacolata Battaglia
Publikováno v:
Epilepsia Open, Vol 9, Iss 1, Pp 258-267 (2024)
Abstract Objective Cardio‐facio‐cutaneous syndrome (CFC) is a genetic disorder due to variants affecting genes coding key proteins of the Ras/MAPK signaling pathway. Among the different features of CFC, neurological involvement, including cerebra
Externí odkaz:
https://doaj.org/article/b1b598bca41f464b845f3dbc403a97a7
Autor:
Roberta Onesimo, Cristiana Agazzi, Luca Massimi, Valentina Giorgio, Chiara Leoni, Giuseppe Zampino, Claudia Rendeli
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-5 (2023)
Abstract Background Down syndrome is a genetic disorder caused by trisomy of chromosome 21 and characterized by an increased risk of multiorgan involvement. In Down syndrome children, functional constipation and lower urinary tract infections have be
Externí odkaz:
https://doaj.org/article/4413a360e2ec485bbf47f63e545190a3
Autor:
Roberta Onesimo, Rita De Santis, Chiara Leoni, Mario Rigante, Marco Piastra, Elisabetta Sforza, Angelo Selicorni, Giuseppe Zampino
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-3 (2023)
Abstract Background Cornelia de Lange syndrome is a rare genetic disease with otolaryngological involvement. The classic phenotype is characterized by distinctive facial features, intellectual disability, growth delay, hirsutism, and upper-limb reduc
Externí odkaz:
https://doaj.org/article/efcfeab4e6fb4f649fb1afb4b7e825c9
Autor:
Danilo Buonsenso, Giulia Poretti, Francesco Mariani, Arianna Turriziani Colonna, Simonetta Costa, Lucia Giordano, Francesca Priolo, Guido Conti, Angelo Tizio, Daniela Rodolico, Giulia Maria Amorelli, Lorenzo Orazi, Maria Petrianni, Daniela Ricci, Antonio Lanzone, Maurizio Sanguinetti, Paola Cattani, Francesca Raffaelli, Michela Sali, Giuseppe Zampino, Giovanni Vento, Piero Valentini
Publikováno v:
Heliyon, Vol 9, Iss 9, Pp e19206- (2023)
Introduction.We performed a single-center, prospective, observational study of newborns born from mothers with microbiologically confirmed SARS-CoV-2 infection in pregnancy or at time of delivery to evaluate acute and mid-term multidisciplinary outco
Externí odkaz:
https://doaj.org/article/38aeb7b6fc414001a490193639dd6110
Autor:
Sara Manti, Annamaria Staiano, Luigi Orfeo, Fabio Midulla, Gian Luigi Marseglia, Chiara Ghizzi, Stefania Zampogna, Virgilio Paolo Carnielli, Silvia Favilli, Martino Ruggieri, Domenico Perri, Giuseppe Di Mauro, Guido Castelli Gattinara, Antonio D’Avino, Paolo Becherucci, Arcangelo Prete, Giuseppe Zampino, Marcello Lanari, Paolo Biban, Paolo Manzoni, Susanna Esposito, Giovanni Corsello, Eugenio Baraldi
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-18 (2023)
Abstract Bronchiolitis is an acute respiratory illness that is the leading cause of hospitalization in young children. This document aims to update the consensus document published in 2014 to provide guidance on the current best practices for managin
Externí odkaz:
https://doaj.org/article/bbf3349da47d4c50b1985a71f7a8ae9b
Autor:
Elisa Maria Turco, Angela Maria Giada Giovenale, Laura Sireno, Martina Mazzoni, Alessandra Cammareri, Caterina Marchioretti, Laura Goracci, Alessandra Di Veroli, Elena Marchesan, Daniel D’Andrea, Antonella Falconieri, Barbara Torres, Laura Bernardini, Maria Chiara Magnifico, Alessio Paone, Serena Rinaldo, Matteo Della Monica, Stefano D’Arrigo, Diana Postorivo, Anna Maria Nardone, Giuseppe Zampino, Roberta Onesimo, Chiara Leoni, Federico Caicci, Domenico Raimondo, Elena Binda, Laura Trobiani, Antonella De Jaco, Ada Maria Tata, Daniela Ferrari, Francesca Cutruzzolà, Gianluigi Mazzoccoli, Elena Ziviani, Maria Pennuto, Angelo Luigi Vescovi, Jessica Rosati
Publikováno v:
Cell Death and Disease, Vol 13, Iss 11, Pp 1-16 (2022)
Abstract Smith-Magenis syndrome (SMS) is a neurodevelopmental disorder characterized by cognitive and behavioral symptoms, obesity, and sleep disturbance, and no therapy has been developed to alleviate its symptoms or delay disease onset. SMS occurs
Externí odkaz:
https://doaj.org/article/3481a3d58ebf491c977d49d933ec8e59
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