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Carolina Putotto

Showing results (1-10 of 57) with videos related to

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Pediatric Cardiology|September 6, 2024
Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac SegmentsCarolina Putotto, Paolo Versacci, Bruno Marino
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.
Anatomical Record (Hoboken, N.J. : 2007)|November 25, 2022
Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspectsAngelo Restivo, Cira di Gioia, Bruno Marino, 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.
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.
Translational Pediatrics|October 10, 2023
Gender differences in congenital heart defects: a narrative reviewFlaminia Pugnaloni, Alessandro Felici, Antonio-Francesco Corno, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
International Clinical Psychopharmacology|October 12, 2023
Efficacy and safety of clozapine in treatment-resistant psychotic patients with DiGeorge syndrome (22q11.2 deletion syndrome): a case seriesIsabella Berardelli, Mariarosaria Cifrodelli, Carlotta Giuliani, et al.
Italian Journal of Pediatrics|March 9, 2021
Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case reportFrancesco Martino, Alessandra Magenta, Maria Letizia Troccoli, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Pediatric Cardiology|September 6, 2024
Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac SegmentsCarolina Putotto, Paolo Versacci, Bruno Marino
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.
Anatomical Record (Hoboken, N.J. : 2007)|November 25, 2022
Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspectsAngelo Restivo, Cira di Gioia, Bruno Marino, 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.
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.
Translational Pediatrics|October 10, 2023
Gender differences in congenital heart defects: a narrative reviewFlaminia Pugnaloni, Alessandro Felici, Antonio-Francesco Corno, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
International Clinical Psychopharmacology|October 12, 2023
Efficacy and safety of clozapine in treatment-resistant psychotic patients with DiGeorge syndrome (22q11.2 deletion syndrome): a case seriesIsabella Berardelli, Mariarosaria Cifrodelli, Carlotta Giuliani, et al.
Italian Journal of Pediatrics|March 9, 2021
Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case reportFrancesco Martino, Alessandra Magenta, Maria Letizia Troccoli, et al.
Pageof 6