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Ettore Piro

Showing results (51-60 of 70) with videos related to

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Pharmaceuticals (Basel, Switzerland)|July 11, 2020
Oxidative Stress in Preterm Infants: Overview of Current Evidence and Future ProspectsRaffaele Falsaperla, Filadelfo Lombardo, Federica Filosco, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlationGiovanni Corsello, Emanuela Salzano, Davide Vecchio, et al.
Italian Journal of Pediatrics|September 29, 2021
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-upGregorio Serra, Vincenzo Antona, Mario Giuffré, et al.
Italian Journal of Pediatrics|December 8, 2021
Developments in pediatrics in 2020: choices in allergy, autoinflammatory disorders, critical care, endocrinology, genetics, infectious diseases, microbiota, neonatology, neurology, nutrition, ortopedics, respiratory tract illnesses and rheumatologyCarlo Caffarelli, Francesca Santamaria, Michela Procaccianti, et al.
Italian Journal of Pediatrics|June 20, 2025
Congenital cytomegalovirus infection and brain injury in a newborn following maternal non-primary infection: case report of an unexpected diagnosisGregorio Serra, Ettore Piro, Deborah Bacile, et al.
Italian Journal of Pediatrics|October 16, 2020
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcomeGregorio Serra, Giovanni Corsello, Vincenzo Antona, et al.
Italian Journal of Pediatrics|February 4, 2022
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case reportIngrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
Italian Journal of Pediatrics|February 10, 2023
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conceptionGregorio Serra, Vincenzo Antona, Marcello Cimador, et al.
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.
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.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Pharmaceuticals (Basel, Switzerland)|July 11, 2020
Oxidative Stress in Preterm Infants: Overview of Current Evidence and Future ProspectsRaffaele Falsaperla, Filadelfo Lombardo, Federica Filosco, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlationGiovanni Corsello, Emanuela Salzano, Davide Vecchio, et al.
Italian Journal of Pediatrics|September 29, 2021
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-upGregorio Serra, Vincenzo Antona, Mario Giuffré, et al.
Italian Journal of Pediatrics|December 8, 2021
Developments in pediatrics in 2020: choices in allergy, autoinflammatory disorders, critical care, endocrinology, genetics, infectious diseases, microbiota, neonatology, neurology, nutrition, ortopedics, respiratory tract illnesses and rheumatologyCarlo Caffarelli, Francesca Santamaria, Michela Procaccianti, et al.
Italian Journal of Pediatrics|June 20, 2025
Congenital cytomegalovirus infection and brain injury in a newborn following maternal non-primary infection: case report of an unexpected diagnosisGregorio Serra, Ettore Piro, Deborah Bacile, et al.
Italian Journal of Pediatrics|October 16, 2020
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcomeGregorio Serra, Giovanni Corsello, Vincenzo Antona, et al.
Italian Journal of Pediatrics|February 4, 2022
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case reportIngrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
Italian Journal of Pediatrics|February 10, 2023
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conceptionGregorio Serra, Vincenzo Antona, Marcello Cimador, et al.
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.
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.
Pageof 7