Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Serena Ascione"'
Autor:
Caterina Monari, Ferdinando Spagnuolo, Mariantonietta Pisaturo, Serena Ascione, Giovanna Donnarumma, Federica Calò, Elisabetta Caredda, Fortunato Montella, Anna Maietta, Paolo Montaldo, Umberto Pugliese, Massimiliano Galdiero, Mauro Carpentieri, Nicola Coppola
Publikováno v:
Infectious Diseases and Therapy, Vol 12, Iss 2, Pp 727-734 (2022)
Abstract Background The prevalence of certain multidrug-resistant organisms (MDROs), especially Gram-negative bacteria, is dramatically increasing in patient care settings, including pediatric and neonatal units. However, most of the new drugs availa
Externí odkaz:
https://doaj.org/article/48c5e552740e4fe5a1efd92655333988
Autor:
Giancarlo Parenti, Giuseppe Di Iorio, Simone Sampaolo, Giuseppe Fiorentino, Vincenzo Farina, Simona Fecarotta, Fabio Valente, Serena Ascione, Mario Caputi, Generoso Andria
Publikováno v:
Cardiogenetics, Vol 3, Iss 1S, Pp e5-e5 (2013)
Pompe disease (glycogenosis type II) is a rare autosomal recessive lysosomal storage disorder due to mutations of the GAA gene, leading to the deficiency of acid α-glucosidase and consequent glycogen storage in various tissues, mainly in the skeleta
Externí odkaz:
https://doaj.org/article/fd641ed5d0d84b90aff8023d526e046c
Autor:
Paolo Montaldo, Simona Puzone, Elisabetta Caredda, Francesca Galdo, Umberto Pugliese, Anna Maietta, Serena Ascione, Mario Diplomatico, Ferdinando Spagnuolo, Vincenzina Roma, Massimiliano De Vivo, Mauro Carpentieri, Sabino Moschella, Lucio Giordano, Alessandra D’Amico, Carlo Capristo, Laura Travan, Giovanni Chello, Emanuele Miraglia del Giudice, Mario Cirillo
Background: There is increasing concern that infants with mild hypoxic-ischaemic encephalopathy (HIE) may develop seizures and progress to moderate HIE beyond the therapeutic window for cooling. Objective: The aim of this study was to examine the eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9312f19ece85506fcb6308ace00d2463
https://hdl.handle.net/11591/486906
https://hdl.handle.net/11591/486906
Autor:
Bruno Minale, Serena Ascione, Carmen Lubrano, Daniela Molino, Vittorio Serio, Gabriele Malgieri, Lorenza Lepore, Carmine Pecoraro, Luigi Annicchiarico Petruzzelli, Ilaria Luongo
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Acute extracorporeal dialysis is a short treatment, performed by a central venous catheter of large size, ensuring high flow. These devices have limitations: high caliber, excessive length, impossibility of tunneling and exit-site
Autor:
Deianira Pedoto, Carmine Pecoraro, Maria Chiara Rocco, Adele Corcione, Luigi Annicchiarico Petruzzelli, Gabriele Malgieri, Diletta Apuzzo, Serena Ascione, Giuseppina Barra
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims We describe the relationship between overweight and obesity and Hypertension on ABPM. Method We conducted a cross-sectional study using a database of patients aged 6-16 years, who had undergone 24h ABPM from December 2002 through
Autor:
Serena Ascione, Diletta Apuzzo, Luigi Annicchiarico Petruzzelli, Carmine Pecoraro, Annamaria Pagano, Giuseppina Barra, Deianira Pedoto, Lorenza Lepore, Gabriele Malgieri, Adele Corcione, Pasquale Barra
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims The goal of our study was to analyze the difference in ABPM pattern in overweight and non overweight hypertensive children Method The ABPM were performed using Spacelab 90207 and recorded over 24h.Readings were taken every 15 minu
Autor:
Carmine Pecoraro, Gabriele Malgieri, Valentina Bruno, Luigi Annicchiarico Petruzzelli, Serena Ascione, Francesca Nuzzi
Publikováno v:
Nephrology Dialysis Transplantation. 34
Autor:
Gaia Scavia, Gabriele Malgieri, Serena Ascione, Marina Noris, Valentina Bruno, Carmine Pecoraro, Elena Bresin, Angela De Luca, Luigi Annicchiarico Petruzzelli, Alfonso Ferretti
Publikováno v:
Nephrology Dialysis Transplantation. 34
Autor:
Giancarlo Parenti, Simona Fecarotta, Alfonso Romano, Giuseppe Montefusco, Generoso Andria, Roberto Della Casa, Ennio Del Giudice, Paola Villari, Serena Ascione
Publikováno v:
Italian Journal of Pediatrics
Aim Dysphagia is a known complication in Pompe Disease (PD), a severe metabolic myopathy due to alpha-glucosidase deficiency. Enzyme replacement therapy (ERT) with alglucosidase alfa is the only approved therapy for PD. Presently no data are availabl
Autor:
G. Parenti, Simone Sampaolo, Fabio Valente, Mario Caputi, Serena Ascione, Giuseppe Di Iorio, Simona Fecarotta, Giuseppe Fiorentino, Vincenzo Farina, Generoso Andria
Publikováno v:
Cardiogenetics, Vol 3, Iss 1S, Pp e5-e5 (2013)
Cardiogenetics
Volume 3
Issue 11
Cardiogenetics
Volume 3
Issue 11
Pompe disease (glycogenosis type II) is a rare autosomal recessive lysosomal storage disorder due to mutations of the GAA gene, leading to the deficiency of acid &alpha
glucosidase and consequent glycogen storage in various tissues, mainly in th
glucosidase and consequent glycogen storage in various tissues, mainly in th