Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bruno Marino

Showing results (21-30 of 156) with videos related to

Pageof 16
Sort By:
Cardiology in the Young|May 20, 2022
Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal geneCarolina Putotto, Elio Caruso, Bruno Marino, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|January 27, 2007
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implicationsGerardo Piacentini, M Cristina Digilio, Anna Sarkozy, et al.
Translational Pediatrics|October 10, 2023
Gender differences in congenital heart defects: a narrative reviewFlaminia Pugnaloni, Alessandro Felici, Antonio-Francesco Corno, et al.
The Annals of Thoracic Surgery|May 9, 2002
Pulmonary atresia with intact ventricular septum and systemic-pulmonary collateral arteriesSonia B Albanese, Adriano Carotti, Alessandra Toscano, et al.
European Journal of Pediatrics|May 31, 2006
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype"M Cristina Digilio, Anna Sarkozy, Giuseppe Pacileo, et al.
Cardiovascular Diseases|June 1, 1981
Morphology of aortic arch obstruction with patent ductus arteriosusBruno Marino, Luigi Chiariello, Corrado Mercanti, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Developmental Disabilities Research Reviews|July 19, 2008
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndromeAdriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, et al.
Birth Defects Research|July 8, 2024
Partial atrioventricular canal defect and aortic coarctation associated with variants in GDF1 and NOTCH1 genes: A case reportCarolina Putotto, Marco Masci, Monia Magliozzi, et al.
Pageof 16

Showing results (21-30 of 156) with videos related to

Sort By:
Pageof 16
Cardiology in the Young|May 20, 2022
Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal geneCarolina Putotto, Elio Caruso, Bruno Marino, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|January 27, 2007
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implicationsGerardo Piacentini, M Cristina Digilio, Anna Sarkozy, et al.
Translational Pediatrics|October 10, 2023
Gender differences in congenital heart defects: a narrative reviewFlaminia Pugnaloni, Alessandro Felici, Antonio-Francesco Corno, et al.
The Annals of Thoracic Surgery|May 9, 2002
Pulmonary atresia with intact ventricular septum and systemic-pulmonary collateral arteriesSonia B Albanese, Adriano Carotti, Alessandra Toscano, et al.
European Journal of Pediatrics|May 31, 2006
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype"M Cristina Digilio, Anna Sarkozy, Giuseppe Pacileo, et al.
Cardiovascular Diseases|June 1, 1981
Morphology of aortic arch obstruction with patent ductus arteriosusBruno Marino, Luigi Chiariello, Corrado Mercanti, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Developmental Disabilities Research Reviews|July 19, 2008
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndromeAdriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, et al.
Birth Defects Research|July 8, 2024
Partial atrioventricular canal defect and aortic coarctation associated with variants in GDF1 and NOTCH1 genes: A case reportCarolina Putotto, Marco Masci, Monia Magliozzi, et al.
Pageof 16