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Bruno Marino

Showing results (81-90 of 156) with videos related to

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American Journal of Medical Genetics. Part A|September 9, 2017
Congenital heart defects in molecularly proven Kabuki syndrome patientsMaria Cristina Digilio, Maria Gnazzo, Francesca Lepri, et al.
International Journal of Cardiology|September 4, 2007
Severe, obstructive biventricular hypertrophy in a patient with Costello syndrome: Clinical impact and managementGiuseppe Limongelli, Giuseppe Pacileo, Maria Cristina Digilio, et al.
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.
Prenatal Diagnosis|April 9, 2024
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluationElizabeth Goldmuntz, Anne S Bassett, Erik Boot, et al.
Journal of Prenatal Medicine|March 23, 2012
Severe, early onset hypertrophic cardiomyopathy in a family with LEOPARD syndromeGiuseppe Limongelli, Giuseppe Pacileo, Maria Giovanna Russo, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|August 28, 2014
Extended normothermic extracorporeal perfusion of isolated human liver after warm ischaemia: a preliminary reportRinaldo Bellomo, Bruno Marino, Graeme Starkey, et al.
Human Mutation|October 1, 2003
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of FallotAntonio Pizzuti, Anna Sarkozy, Anthea L Newton, et al.
Frontiers in Pediatrics|May 8, 2026
Morphological and functional echocardiographic findings in pediatric patients diagnosed with hypermobile Ehlers-Danlos syndromeWalter Vignaroli, Gioia Mastromoro, Carolina Putotto, et al.
Early Intervention in Psychiatry|March 29, 2022
Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndromeAntonino Buzzanca, Tommaso Accinni, Marianna Frascarelli, 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.
Pageof 16

Showing results (81-90 of 156) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Part A|September 9, 2017
Congenital heart defects in molecularly proven Kabuki syndrome patientsMaria Cristina Digilio, Maria Gnazzo, Francesca Lepri, et al.
International Journal of Cardiology|September 4, 2007
Severe, obstructive biventricular hypertrophy in a patient with Costello syndrome: Clinical impact and managementGiuseppe Limongelli, Giuseppe Pacileo, Maria Cristina Digilio, et al.
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.
Prenatal Diagnosis|April 9, 2024
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluationElizabeth Goldmuntz, Anne S Bassett, Erik Boot, et al.
Journal of Prenatal Medicine|March 23, 2012
Severe, early onset hypertrophic cardiomyopathy in a family with LEOPARD syndromeGiuseppe Limongelli, Giuseppe Pacileo, Maria Giovanna Russo, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|August 28, 2014
Extended normothermic extracorporeal perfusion of isolated human liver after warm ischaemia: a preliminary reportRinaldo Bellomo, Bruno Marino, Graeme Starkey, et al.
Human Mutation|October 1, 2003
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of FallotAntonio Pizzuti, Anna Sarkozy, Anthea L Newton, et al.
Frontiers in Pediatrics|May 8, 2026
Morphological and functional echocardiographic findings in pediatric patients diagnosed with hypermobile Ehlers-Danlos syndromeWalter Vignaroli, Gioia Mastromoro, Carolina Putotto, et al.
Early Intervention in Psychiatry|March 29, 2022
Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndromeAntonino Buzzanca, Tommaso Accinni, Marianna Frascarelli, 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.
Pageof 16