Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Caterina, Lambiase"'
Autor:
Francesca Crea, Filippo Maria Panfili, Maria Elisa Amodeo, Danilo Fintini, Francesco Paolo Rossi, Italo Trenta, Alessandra Menichella, Chiara Ossella, Andrea Deidda, Roberta Lidano, Giulia Macchiarulo, Caterina Lambiase, Maria Antonietta Barbieri, Massimiliano Raponi
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-10 (2021)
Abstract Background Numerous studies described the epidemiological link and main clinical features of pediatric COVID-19, during the first pandemic period. Our study encompasses several different phases since the National Lockdown in Italy. The prima
Externí odkaz:
https://doaj.org/article/b27e3a7b7cca496cabff79c36179ff34
Autor:
Raffaella Nenna, Fabio Midulla, Caterina Lambiase, Giovanna De Castro, Anna Maria Zicari, Luciana Indinnimeo, Giuseppe Cimino, Patrizia Troiani, Serena Quattrucci, Giancarlo Tancredi
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-6 (2017)
Abstract Background This crossover, randomized, double-blind study (conducted over a 32-week period) was performed to determine, in clinically stable Cystic fibrosis (CF) preschool children: the effects of 7% inhaled hypertonic saline on spirometry a
Externí odkaz:
https://doaj.org/article/c0b0ee3863db47f4945c8932f382cc38
Autor:
Gioia Mastromoro, Giulio Calcagni, Paolo Versacci, Carolina Putotto, Marcello Chinali, Caterina Lambiase, Marta Unolt, Elena Pelliccione, Silvia Anaclerio, Cinzia Caprio, Sara Cioffi, Marchesa Bilio, Anwar Baban, Fabrizio Drago, Maria Cristina Digilio, Bruno Marino, Antonio Baldini
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0211170 (2019)
INTRODUCTION AND HYPOTHESIS:Patients with 22q11 deletion syndrome (22q11.2DS) present, in about 75% of cases, typical patterns of cardiac defects, with a particular involvement on the ventricular outflow tract and great arteries. However, in this gen
Externí odkaz:
https://doaj.org/article/b11194a58e96490993baa88b1b30daeb
Autor:
Carolina Putotto, Marta Unolt, Caterina Lambiase, Flaminia Marchetti, Silvia Anaclerio, Alessandra Favoriti, Giancarlo Tancredi, Gioia Mastromoro, Flaminia Pugnaloni, Natascia Liberati, Enrica De Luca, Luigi Tarani, Daniela De Canditiis, Viviana Caputo, Laura Bernardini, Maria Cristina Digilio, Bruno Marino, Paolo Versacci
Publikováno v:
European Journal of Medical Genetics. 66:104651
Diagnosis and treatment of 22q11.2 deletion syndrome (22q11.2DS) have led to improved life expectancy and achievement of adulthood. Limited data on long-term outcomes reported an increased risk of premature death for cardiovascular causes, even witho
Autor:
Roberta Lidano, Alessandra Menichella, Maria Antonietta Barbieri, Caterina Lambiase, Filippo Maria Panfili, Italo Trenta, Giulia Macchiarulo, Francesca Crea, Danilo Fintini, Francesco Paolo Rossi, Maria Elisa Amodeo, Andrea Deidda, Chiara Ossella, Massimiliano Raponi
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-10 (2021)
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-10 (2021)
Background Numerous studies described the epidemiological link and main clinical features of pediatric COVID-19, during the first pandemic period. Our study encompasses several different phases since the National Lockdown in Italy. The primary outcom
Autor:
Italo Trenta, Francesca Crea, M.A. Barbieri, A. Menichella, Lidano R, Caterina Lambiase, Giulia Macchiarulo, Filippo Maria Panfili, Massimiliano Raponi, Chiara Ossella, Andrea Deidda, Francesco Paolo Rossi, Amodeo Me, Danilo Fintini
Publikováno v:
SSRN Electronic Journal.
Background: Numerous studies described the epidemiological link and main clinical features of pediatric COVID-19, during the first pandemic period, while this is the first study that encompass several different phases of National Lockdown in a Europe
Autor:
Claudio Colonnese, Alessandra Morano, Marco Ceccanti, Antonino Buzzanca, Massimo Biondi, Antonio Pizzuti, Martina Fanella, Marianna Frascarelli, Alfredo Berardelli, Carlo Di Bonaventura, Caterina Lambiase, Alessandro Viganò, Jinane Fattouch, Natascia Liberati, Fabio Di Fabio, Marta Unolt, Tommaso Accinni, Anna Teresa Giallonardo
Background22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophrenia. However, its polymorphic nature has led researchers to further investigate its neuropsychiatric manifestations.MethodsWe enrolled 56 adults (38 men,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91ccd9298d76ccb3de503775755711e
http://hdl.handle.net/11573/1462070
http://hdl.handle.net/11573/1462070
Autor:
Maria Cristina Digilio, Donna M. McDonald-McGinn, Paolo Versacci, Elizabeth Goldmuntz, Marta Unolt, Terrence B. Crowley, Elaine H. Zackai, Caterina Lambiase, Adriano Carotti, Giulio Calcagni, Bruno Marino, Silvia Anaclerio, Matteo Trezzi, James W Gaynor
Congenital heart diseases (CHDs) and cardiovascular abnormalities are one of the pillars of clinical diagnosis of 22q11.2 deletion syndrome (22q11.2DS) and still represent the main cause of mortality in the affected children. In the past 30 years, mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a19aae91c9ce7a62759dc6dd338993
https://europepmc.org/articles/PMC6497171/
https://europepmc.org/articles/PMC6497171/
Publikováno v:
Advances in experimental medicine and biology. 1000
Exercise represents an important lifestyle factor in all human ages when felt in harmony with other psycho-physical and environmental variables that affect individual life (e. g. quality of interest, affections, environment, diet and food). Consequen
Publikováno v:
Minerva Respiratory Medicine. 56