Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Gabriella DE ROSA"'
Autor:
Donato Rigante, Gabriella De Rosa, Angelica Bibiana Delogu, Giulia Rotunno, Rossella Cianci, Claudia Di Pangrazio, Giorgio Sodero, Umberto Basile, Marcello Candelli
Publikováno v:
Diagnostics, Vol 14, Iss 12, p 1228 (2024)
Introduction: An aberrant immune response involving yet unidentified environmental and genetic factors plays a crucial role in triggering Kawasaki disease (KD). Aims: The aim of this study was to assess general and laboratory data at the onset of KD
Externí odkaz:
https://doaj.org/article/d82569f9f33d4250befb78437cc0016f
Publikováno v:
Fire, Vol 6, Iss 3, p 91 (2023)
The main objective of this study is to compare the results in terms of gas temperature and structural elements temperature, using different localized fire models. In particular, with reference to an open car park fire, the simplified Hasemi localized
Externí odkaz:
https://doaj.org/article/e27eaf2a4bdb4ba6a5333e8b353b691c
Autor:
Alessandro Gambacorta, Danilo Buonsenso, Gabriella De Rosa, Ilaria Lazzareschi, Antonio Gatto, Federica Brancato, Davide Pata, Piero Valentini
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Kawasaki disease (KD) is an acute, febrile illness of unknown etiology that mainly affects children under 5 years of age. intravenous immunoglobulin (IVIG), the standard treatment, has reduced coronary involvement to
Externí odkaz:
https://doaj.org/article/3f1b0bf190b444e8be1a45229666e07d
Autor:
Giorgio Sodero, Francesco Mariani, Francesco Proli, Ilaria Lazzareschi, Giulia Bersani, Angelica Bibiana Delogu, Gabriella De Rosa, Giuseppe Zampino, Piero Valentini, Danilo Buonsenso
Publikováno v:
Acta Paediatrica. 112:1038-1040
Autor:
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, Rachele Adorisio, Juan Pablo Kaski, Rita Blandino, Stella Maiolo, Emanuele Monda, Carolina Putotto, Gabriella De Rosa, Kathryn C. Chatfield, Bruce D. Gelb, Giulio Calcagni
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical geneticsREFERENCES. 190(4)
The cardiovascular phenotype associated with RASopathies has expanded far beyond the original descriptions of pulmonary valve stenosis by Dr Jaqueline Noonan in 1968 and hypertrophic cardiomyopathy by Hirsch et al. in 1975. Because of the common unde
Autor:
Alessia Nunziata, Marcello Covino, Antonio Chiaretti, Gabriella De Rosa, Alessandro Gambacorta, Federica Brancato, Pietro Ferrara, Danilo Buonsenso
Publikováno v:
Pediatric Emergency Care. 37:e1589-e1592
Chest pain is a common cause to admission to the pediatric emergency department and often leads to an extensive cardiac evaluation. The objective of this study was to evaluate the usefulness of the troponin (TN) plasma level determination in the init
Autor:
Marco Piastra, Alessia Tempera, Tony Christian Morena, Lucilla Pezza, Vittoria Ferrari, Maria Cristina Fedele, Enzo Picconi, Giorgio Conti, Gabriella De Rosa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0f6c77afa934cf11f4fdaa9f784f53a
https://hdl.handle.net/10807/226027
https://hdl.handle.net/10807/226027
Autor:
Roberta Onesimo, Angelica Bibiana Delogu, Gaetano Antonio Lanza, Giuseppe Zampino, Rita Blandino, Gabriella De Rosa, Donato Rigante, Marco Tartaglia, Valeria Verusio, Chiara Leoni, Maria Vittoria Marino
Congenital heart disease (CHD) and hypertrophic cardiomyopathy (HCM) are common features in patients affected by RASopathies. The aim of this study was to assess genotype- phenotype correlations, focusing on the cardiac features and outcomes of inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42059ad814313ef249015b5a21718c2a
http://hdl.handle.net/10807/193501
http://hdl.handle.net/10807/193501
Autor:
Alessandro Gambacorta, Federica Brancato, Claudia Aurilia, Donato Rigante, Marco Piastra, Gabriella De Rosa
Publikováno v:
Paediatrics and international child health. 41(4)
Background: Myocardial bridging is largely considered to be a benign, symptomless congenital anomaly of the coronary arteries in which the intramyocardial coronary course is partially 'tunnelled' and leads to vessel compression during ventricular sys
Autor:
Roberta Onesimo, Giuseppe Zampino, Paolo Versacci, Gabriella De Rosa, Giulio Calcagni, Marcella Zollino, Maria Cristina Digilio, Bruno Marino, Chiara Leoni, Angelica Bibiana Delogu, Flaminia Pugnaloni, Rita Blandino
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(7)
Smith-Magenis syndrome (SMS) is a genetic disorder characterized by multiple congenital anomalies, sleep disturbance, behavioral impairment, and intellectual disability. Its genetic cause has been defined as an alteration in the Retinoic Acid-Induced