Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Gerardo Piacentini"'
Autor:
Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Laura Bernardini, Antonella Giancotti, Gerardo Piacentini, Alessandro De Luca, Antonio Pizzuti
Publikováno v:
Diagnostics, Vol 13, Iss 1, p 48 (2022)
Fetal Nuchal fluid collections can manifest with two distinct presentations attributable to the same phenotypic spectrum: increased nuchal translucency (iNT) and cystic hygroma. The prenatal detection of these findings should prompt an accurate asses
Externí odkaz:
https://doaj.org/article/c64ca71febf946c8a8bcb74933338c65
Autor:
Gioia Mastromoro, Nader Khaleghi Hashemian, Daniele Guadagnolo, Maria Grazia Giuffrida, Barbara Torres, Laura Bernardini, Flavia Ventriglia, Gerardo Piacentini, Antonio Pizzuti
Publikováno v:
Diagnostics, Vol 12, Iss 6, p 1328 (2022)
Cardiovascular malformations (CVM) represent the most common structural anomalies, occurring in 0.7% of live births. The CVM prenatal suspicion should prompt an accurate investigation with fetal echocardiography and the assessment through genetic cou
Externí odkaz:
https://doaj.org/article/2fb2ac172a94405fbae6a7fee28359f8
Publikováno v:
Circulation: Cardiovascular Imaging.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c666227550c51c0b33742033cbcbe04
https://doi.org/10.1161/circimaging.122.014658
https://doi.org/10.1161/circimaging.122.014658
Autor:
Roberto Formigari, Maria Cristina Digilio, Bruno Marino, Adriano Carotti, Gerardo Piacentini, Guido Michielon, Roberto M. Di Donato, Alessandro Giardini
Publikováno v:
European Journal of Cardio-Thoracic Surgery. 35:606-614
The population of neonates and children with congenital heart defects presents about a 30% prevalence of associated genetic syndrome or additional extracardiac anomalies and may show an increased risk of death or major complication at cardiac surgery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3bc01bbd697614a68eed35453832a26
https://doi.org/10.1016/j.ejcts.2008.11.005
https://doi.org/10.1016/j.ejcts.2008.11.005
Autor:
Bruno Marino, Adriano Carotti, Maria Cristina Digilio, Claudia Saffirio, Gerardo Piacentini, Roberto M. Di Donato
Publikováno v:
Developmental Disabilities Research Reviews. 14:35-42
Specific types and subtypes of cardiac defects have been described in children with 22q11.2 deletion syndrome as well as in other genetic syndromes. The conotruncal heart defects occurring in patients with 22q11.2 deletion syndrome include tetralogy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a6a0b1e6aaa98a535c392c9ea8f678f
https://doi.org/10.1002/ddrr.6
https://doi.org/10.1002/ddrr.6
Autor:
Silvia Placidi, Anna Sarkozy, Bruno Dallapiccola, Bruno Marino, M. Cristina Digilio, Gerardo Piacentini
Congenital heart defects (CHDs) are the most common birth defects in humans and over the last 20 years significant progress has been made in the understanding of the molecular and genetic determinants of an increasing number of CHDs. Fundamental to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb20f2b569ec3df088de5814f9c98c9
http://hdl.handle.net/11573/232072
http://hdl.handle.net/11573/232072
Cardiac outflow tract: a review of some embryogenetic aspects of the conotruncal region of the heart
Publikováno v:
The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology. 288(9)
A review concerning some embryogenetic aspects of the cardiac outflow tract is presented. Two main topics are discussed: the truncal septation and the secondary heart field. In the context of the septation of the truncus arteriosus, the development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a411c271458bc95a4845f935eeec303
https://pubmed.ncbi.nlm.nih.gov/16892424
https://pubmed.ncbi.nlm.nih.gov/16892424
Autor:
Bruno Dallapiccola, Bruno Marino, Maurizio Marasini, M. Cristina Digilio, Gerardo Piacentini, Alessandra Toscano, Anna Sarkozy, Andrea Zorzi, Rita D'Agostino, M. Giovanna Russo, Rossella Capolino
Publikováno v:
American journal of medical genetics. Part A. 137(2)
Familial recurrence of congenitally corrected transposition of the great arteries (CCTGA) is considered uncommon. Most of the previous familial studies involved a small number of patients and referred to all situs and looping anomalies including sing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6acec87b2cad6f6289df2ccce35a166d
https://pubmed.ncbi.nlm.nih.gov/16059940
https://pubmed.ncbi.nlm.nih.gov/16059940
Publikováno v:
The Lancet. 368:1963-1964
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13ba5f887f7c2764e7ba8b753dd9feb
https://doi.org/10.1016/s0140-6736(06)69804-8
https://doi.org/10.1016/s0140-6736(06)69804-8