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Marta Unolt

Showing results (11-20 of 34) with videos related to

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Genes|December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center StudyCarolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
22q and two: 22q11.2 deletion syndrome and coexisting conditionsJennifer L Cohen, Terrence B Crowley, Daniel E McGinn, et al.
American Journal of Medical Genetics. Part A|May 2, 2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literatureGioia Mastromoro, Giulio Calcagni, Walter Vignaroli, et al.
Genes|August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New InsightsGiulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
The Journal of Pediatrics|July 3, 2018
Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based ExperienceFabrizio Drago, Camilla Calvieri, Silvia Placidi, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 22, 2024
Long-term incidence of arrhythmias in extracardiac conduit Fontan and comparison between systemic left and right ventricleCorrado Di Mambro, Marie Laure Yammine, Pietro Paolo Tamborrino, et al.
European Journal of Medical Genetics|February 16, 2018
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndromeMarta Unolt, Jessica Barry, Maria Cristina Digilio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive conditionMarta Unolt, Molka Kammoun, Beata Nowakowska, et al.
American Journal of Medical Genetics. Part A|April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiersMarta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
Genes|January 21, 2023
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective StudyHayley A Ron, Terrence Blaine Crowley, Yichuan Liu, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Genes|December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center StudyCarolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
22q and two: 22q11.2 deletion syndrome and coexisting conditionsJennifer L Cohen, Terrence B Crowley, Daniel E McGinn, et al.
American Journal of Medical Genetics. Part A|May 2, 2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literatureGioia Mastromoro, Giulio Calcagni, Walter Vignaroli, et al.
Genes|August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New InsightsGiulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
The Journal of Pediatrics|July 3, 2018
Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based ExperienceFabrizio Drago, Camilla Calvieri, Silvia Placidi, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 22, 2024
Long-term incidence of arrhythmias in extracardiac conduit Fontan and comparison between systemic left and right ventricleCorrado Di Mambro, Marie Laure Yammine, Pietro Paolo Tamborrino, et al.
European Journal of Medical Genetics|February 16, 2018
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndromeMarta Unolt, Jessica Barry, Maria Cristina Digilio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive conditionMarta Unolt, Molka Kammoun, Beata Nowakowska, et al.
American Journal of Medical Genetics. Part A|April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiersMarta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
Genes|January 21, 2023
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective StudyHayley A Ron, Terrence Blaine Crowley, Yichuan Liu, et al.
Pageof 4