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Marta Unolt

Showing results (1-10 of 34) with videos related to

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Anatomical Record (Hoboken, N.J. : 2007)|February 13, 2013
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defectsAngelo Restivo, Marta Unolt, Carolina Putotto, et al.
Genome Medicine|August 13, 2024
Laterality, heterotaxy, and isolated congenital heart defects : The genetic basis of the segmental nature of the heartCarolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Journal of Cardiovascular Development and Disease|May 5, 2018
Some Isolated Cardiac Malformations Can Be Related to Laterality DefectsPaolo Versacci, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
Expert Review of Molecular Diagnostics|July 27, 2017
Congenital heart disease and genetic syndromes: new insights into molecular mechanismsGiulio Calcagni, Marta Unolt, Maria Cristina Digilio, et al.
Frontiers in Pediatrics|January 9, 2014
Transposition of great arteries: new insights into the pathogenesisMarta Unolt, Carolina Putotto, Lucia M Silvestri, et al.
American Journal of Medical Genetics. Part A|December 22, 2015
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndromeFrancesca Clementina Radio, Maria Cristina Digilio, Rossella Capolino, et al.
Pacing and Clinical Electrophysiology : PACE|April 2, 2020
Left ventricular (LV) pacing in newborns and infants: Echo assessment of LV systolic function and synchrony at 5-year follow-upMassimo Stefano Silvetti, Giulia Muzi, Marta Unolt, et al.
Children (Basel, Switzerland)|June 24, 2022
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart DefectsCarolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
American Journal of Medical Genetics. Part A|September 30, 2016
Congenital diaphragmatic hernia in 22q11.2 deletion syndromeMarta Unolt, Lauren DiCairano, Kathryn Schlechtweg, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Anatomical Record (Hoboken, N.J. : 2007)|February 13, 2013
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defectsAngelo Restivo, Marta Unolt, Carolina Putotto, et al.
Genome Medicine|August 13, 2024
Laterality, heterotaxy, and isolated congenital heart defects : The genetic basis of the segmental nature of the heartCarolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Journal of Cardiovascular Development and Disease|May 5, 2018
Some Isolated Cardiac Malformations Can Be Related to Laterality DefectsPaolo Versacci, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
Expert Review of Molecular Diagnostics|July 27, 2017
Congenital heart disease and genetic syndromes: new insights into molecular mechanismsGiulio Calcagni, Marta Unolt, Maria Cristina Digilio, et al.
Frontiers in Pediatrics|January 9, 2014
Transposition of great arteries: new insights into the pathogenesisMarta Unolt, Carolina Putotto, Lucia M Silvestri, et al.
American Journal of Medical Genetics. Part A|December 22, 2015
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndromeFrancesca Clementina Radio, Maria Cristina Digilio, Rossella Capolino, et al.
Pacing and Clinical Electrophysiology : PACE|April 2, 2020
Left ventricular (LV) pacing in newborns and infants: Echo assessment of LV systolic function and synchrony at 5-year follow-upMassimo Stefano Silvetti, Giulia Muzi, Marta Unolt, et al.
Children (Basel, Switzerland)|June 24, 2022
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart DefectsCarolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
American Journal of Medical Genetics. Part A|September 30, 2016
Congenital diaphragmatic hernia in 22q11.2 deletion syndromeMarta Unolt, Lauren DiCairano, Kathryn Schlechtweg, et al.
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