Zobrazeno 1 - 10
of 201
pro vyhledávání: '"Guido, Oppido"'
Publikováno v:
Annals of Pediatric Cardiology, Vol 15, Iss 3, Pp 291-293 (2022)
We report a rare case of vascular ring due to a left cervical circumflex aortic arch with aberrant right subclavian artery arising from a Kommerell diverticulum. This is a very rare case of vascular ring in a newborn with stridor and stenosis of the
Externí odkaz:
https://doaj.org/article/1e20b523636047c88f1fda078b6ed92f
Autor:
Berardo Sarubbi, Gabriella Farina, Diego Colonna, Anna Correra, Emanuele Romeo, Giovanni Domenico Ciriello, Guido Oppido, Maria Giovanna Russo
Publikováno v:
Monaldi Archives for Chest Disease (2022)
Placement of traditional transvenous implantable cardioverter defibrillator (ICD) system in low-weight children is often difficult because of their vessel size, the elevated risk of lead malfunction and failure, children’s growth and various anatom
Externí odkaz:
https://doaj.org/article/6843a70f702c4a1d8ee028aa739c07a6
Autor:
Alessandro Giamberti, Federica Caldaroni, Alessandro Varrica, Carlo Pace Napoleone, Stefano Maria Marianeschi, Nicola Uricchio, Vittorio Vanini, Francesco Santoro, Giovanni Battista Luciani, Giovanni Stellin, Gaetano Gargiulo, Bruno Murzi, Sergio Filippelli, Guido Oppido, Salvatore Agati, Lorenzo Galletti, Alessandro Frigiola
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
More than 4 millions of children with congenital heart disease (CHD) are waiting for cardiac surgery around the world. Few of these patients are treated only thanks to the support of many non-governmental organizations (NGOs). Starting in December 20
Externí odkaz:
https://doaj.org/article/68c15daf0da44ca6b0cb7d519b1004e1
Publikováno v:
Annals of Pediatric Cardiology, Vol 15, Iss 4, Pp 429-430 (2022)
Cor triatriatum dexter is an extremely rare congenital anomaly that is caused by the partitioning of the right atrium by a broad sheet of tissue due to the persistence of the right sinus venosus valve. We describe a rare case of prominent right sinus
Externí odkaz:
https://doaj.org/article/68988171f4c74f0788f7a3ce2a45451b
Publikováno v:
JTCVS Techniques.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7583c429b0fe0ca67ed0d3621c88f130
https://doi.org/10.1016/j.xjtc.2023.03.011
https://doi.org/10.1016/j.xjtc.2023.03.011
Autor:
Gabriele Scalzo, Luigi Arcieri, Vitali Pak, Federico Brunelli, Guido Oppido, Alessandro Varrica, Alessandro Giamberti, Stefano M. Marianeschi, Salvatore Agati, Lorenzo Galletti, Carlo Pace Napoleone, Giovanni Battista Luciani, Gaetano Palma, Gaetano Gargiulo, Massimo A. Padalino
Publikováno v:
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-thoracic Surgery
European Journal of Cardio-Thoracic Surgery
European Journal of Cardio-Thoracic Surgery
OBJECTIVES Italy has been one of the countries most severely affected by the coronavirus disease 2019 (COVID-19). The Italian government was forced to introduce quarantine measures quickly, and all elective health services were stopped or postponed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::217e22753016a72941891346a40d5ef7
http://europepmc.org/articles/PMC7717236
http://europepmc.org/articles/PMC7717236
Publikováno v:
The Annals of thoracic surgery. 112(4)
Type A aortic dissection is a very uncommon finding in children, especially among infants, where no cases seem to have been described. We report the case of an 11-month-old boy with Loeys-Dietz syndrome and asymptomatic type A aortic dissection invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::891d8f5ca35895cd1dc7a2ab548640a1
https://pubmed.ncbi.nlm.nih.gov/33549521
https://pubmed.ncbi.nlm.nih.gov/33549521
Autor:
Stefano Nistri, Pietro Strisciuglio, Emanuele Monda, Guido Oppido, Angelina Grammegna, Mariagiovanna Russo, Alessandro Della Corte, Adelaide Fusco, Martina Caiazza, Annapaola Cirillo, Paolo Calabrò, Guglielmina Pepe, Augusto Esposito, Marta Rubino, Giuseppe Limongelli, Alfredo Mauriello, Felice Gragnano, Daniela Melis
Background:Marfan syndrome is an autosomal dominant disorder of the connective tissue, whose cardinal features affect eyes, musculoskeletal, and cardiovascular system. Despite prevalence and natural history of cardiovascular manifestation are well kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73974d0b32e6e5f690f86d25d24ecbb6
http://hdl.handle.net/11386/4741347
http://hdl.handle.net/11386/4741347
Publikováno v:
Cardiology Research and Practice, Vol 2009 (2009)
Externí odkaz:
https://doaj.org/article/e99345a969e84d3895775224a83cafb4
Autor:
Raffaella Brunetti-Pierri, Vincenzo Nigro, Annalaura Torella, Guido Oppido, Nicola Brunetti-Pierri, Marianna Alagia, Gerarda Cappuccio, Giuseppe Limongelli, Francesca Simonelli, Michele Pinelli, Tudp
Publikováno v:
American Journal of Medical Genetics. Part a
Myhre syndrome is a rare autosomal dominant disorder caused by a narrow spectrum of missense mutations in the SMAD4 gene. Typical features of this disorder are distinctive facial appearance, deafness, intellectual disability, cardiovascular abnormali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbf774781b009607e2f6edbedcf5934
http://europepmc.org/articles/PMC5814867
http://europepmc.org/articles/PMC5814867