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Anne Mandy

Showing results (51-60 of 61) with videos related to

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Italian Journal of Pediatrics|September 19, 2023
Report and follow-up on two new patients with congenital mesoblastic nephromaGregorio Serra, Marcello Cimador, Mario Giuffrè, et al.
Journal of Clinical Medicine|February 27, 2026
Neonatal Esophageal Perforation: A Comprehensive Review of the LiteratureGregorio Serra, Veronica Notarbartolo, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|January 28, 2018
Etiological heterogeneity and clinical variability in newborns with esophageal atresiaEttore Piro, Ingrid Anne Mandy Schierz, Mario Giuffrè, et al.
Frontiers in Pediatrics|June 15, 2026
Iatrogenic esophageal perforation in extremely preterm newborn with multiple comorbidities: case report and ethical considerationsGregorio Serra, Veronica Notarbartolo, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|December 29, 2022
Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restrictionGregorio Serra, Maurizio Carta, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|December 16, 2025
SARS-CoV-2 infection during pregnancy and necrotizing enterocolitis: case report and review of the literatureGregorio Serra, Marco Pensabene, Deborah Bacile, et al.
Italian Journal of Pediatrics|December 29, 2022
Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 geneGregorio Serra, Vincenzo Antona, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|April 14, 2024
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcomeGregorio Serra, Vincenzo Antona, Vincenzo Insinga, et al.
Italian Journal of Pediatrics|September 8, 2022
Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndromeGregorio Serra, Clara Giambrone, Vincenzo Antona, et al.
Journal of Clinical Medicine|June 13, 2025
Novel Compound Heterozygous Mutation of the <i>ABCA3</i> Gene in a Patient with Neonatal-Onset Interstitial Lung DiseaseGregorio Serra, Veronica Notarbartolo, Vincenzo Antona, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Italian Journal of Pediatrics|September 19, 2023
Report and follow-up on two new patients with congenital mesoblastic nephromaGregorio Serra, Marcello Cimador, Mario Giuffrè, et al.
Journal of Clinical Medicine|February 27, 2026
Neonatal Esophageal Perforation: A Comprehensive Review of the LiteratureGregorio Serra, Veronica Notarbartolo, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|January 28, 2018
Etiological heterogeneity and clinical variability in newborns with esophageal atresiaEttore Piro, Ingrid Anne Mandy Schierz, Mario Giuffrè, et al.
Frontiers in Pediatrics|June 15, 2026
Iatrogenic esophageal perforation in extremely preterm newborn with multiple comorbidities: case report and ethical considerationsGregorio Serra, Veronica Notarbartolo, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|December 29, 2022
Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restrictionGregorio Serra, Maurizio Carta, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|December 16, 2025
SARS-CoV-2 infection during pregnancy and necrotizing enterocolitis: case report and review of the literatureGregorio Serra, Marco Pensabene, Deborah Bacile, et al.
Italian Journal of Pediatrics|December 29, 2022
Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 geneGregorio Serra, Vincenzo Antona, Maria Rita Di Pace, et al.
Italian Journal of Pediatrics|April 14, 2024
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcomeGregorio Serra, Vincenzo Antona, Vincenzo Insinga, et al.
Italian Journal of Pediatrics|September 8, 2022
Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndromeGregorio Serra, Clara Giambrone, Vincenzo Antona, et al.
Journal of Clinical Medicine|June 13, 2025
Novel Compound Heterozygous Mutation of the <i>ABCA3</i> Gene in a Patient with Neonatal-Onset Interstitial Lung DiseaseGregorio Serra, Veronica Notarbartolo, Vincenzo Antona, et al.
Pageof 7