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Pediatric Cardiology
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September 6, 2024
Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac Segments
Carolina Putotto, Paolo Versacci, Bruno Marino
Anatomical Record (Hoboken, N.J. : 2007)
|
February 13, 2013
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects
Angelo 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 aspects
Angelo 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 heart
Carolina 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 gene
Carolina Putotto, Elio Caruso, Bruno Marino, et al.
Translational Pediatrics
|
October 10, 2023
Gender differences in congenital heart defects: a narrative review
Flaminia 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 defects
Flaminia 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 series
Isabella 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 report
Francesco Martino, Alessandra Magenta, Maria Letizia Troccoli, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Pediatric Cardiology
|
September 6, 2024
Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac Segments
Carolina Putotto, Paolo Versacci, Bruno Marino
Anatomical Record (Hoboken, N.J. : 2007)
|
February 13, 2013
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects
Angelo 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 aspects
Angelo 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 heart
Carolina 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 gene
Carolina Putotto, Elio Caruso, Bruno Marino, et al.
Translational Pediatrics
|
October 10, 2023
Gender differences in congenital heart defects: a narrative review
Flaminia 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 defects
Flaminia 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 series
Isabella 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 report
Francesco Martino, Alessandra Magenta, Maria Letizia Troccoli, et al.
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of 6