Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ettore Piro

Showing results (41-50 of 70) with videos related to

Pageof 7
Sort By:
Italian Journal of Pediatrics|November 28, 2025
Pediatrics advances in 2024: choices in allergy, cardiology, critical care, endocrinology, gastroenterology, immunology, infectious diseases, neonatology, nephrology, neurology, nutrition, palliative care respiratory tract illnesses, and social mediaCarlo Caffarelli, Elena Bozzola, Ettore Piro, et al.
Frontiers in Pediatrics|December 3, 2021
Case Report: Unusual Clinical Presentation of a Rare Cardiac Inflammatory Myofibroblastic Tumor in Children: The Differential Diagnosis With Pediatric EmergenciesClio Bilotta, Giulio Perrone, Emiliano Maresi, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 5, 2022
Clinical and genetic approach in the characterization of newborns with anorectal malformationIngrid Anne Mandy Schierz, Ettore Piro, Mario Giuffrè, et al.
Italian Journal of Pediatrics|August 19, 2022
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 geneFrancesca Mercadante, Ettore Piro, Martina Busè, et al.
American Journal of Perinatology|March 5, 2013
Predictive factors of abdominal compartment syndrome in neonatal ageIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Journal of Applied Genetics|May 1, 2012
Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGHChiara Donatella Viaggi, Simona Cavani, Mauro Pierluigi, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A premature infant with Costello syndrome due to a rare G13C HRAS mutationMaria Piccione, Ettore Piro, Maria Grazia Pomponi, et al.
European Journal of Medical Genetics|March 13, 2012
Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlationMaria Piccione, Ettore Piro, Francesca Serraino, et al.
Italian Journal of Pediatrics|September 25, 2020
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patientEttore Piro, Gregorio Serra, Vincenzo Antona, et al.
Italian Journal of Pediatrics|February 22, 2025
KBG syndrome: report and follow-up on three unrelated patients observed at different agesGregorio Serra, Pierandrea Elefante, Ylenia Gazzitano, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Italian Journal of Pediatrics|November 28, 2025
Pediatrics advances in 2024: choices in allergy, cardiology, critical care, endocrinology, gastroenterology, immunology, infectious diseases, neonatology, nephrology, neurology, nutrition, palliative care respiratory tract illnesses, and social mediaCarlo Caffarelli, Elena Bozzola, Ettore Piro, et al.
Frontiers in Pediatrics|December 3, 2021
Case Report: Unusual Clinical Presentation of a Rare Cardiac Inflammatory Myofibroblastic Tumor in Children: The Differential Diagnosis With Pediatric EmergenciesClio Bilotta, Giulio Perrone, Emiliano Maresi, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 5, 2022
Clinical and genetic approach in the characterization of newborns with anorectal malformationIngrid Anne Mandy Schierz, Ettore Piro, Mario Giuffrè, et al.
Italian Journal of Pediatrics|August 19, 2022
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 geneFrancesca Mercadante, Ettore Piro, Martina Busè, et al.
American Journal of Perinatology|March 5, 2013
Predictive factors of abdominal compartment syndrome in neonatal ageIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Journal of Applied Genetics|May 1, 2012
Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGHChiara Donatella Viaggi, Simona Cavani, Mauro Pierluigi, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A premature infant with Costello syndrome due to a rare G13C HRAS mutationMaria Piccione, Ettore Piro, Maria Grazia Pomponi, et al.
European Journal of Medical Genetics|March 13, 2012
Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlationMaria Piccione, Ettore Piro, Francesca Serraino, et al.
Italian Journal of Pediatrics|September 25, 2020
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patientEttore Piro, Gregorio Serra, Vincenzo Antona, et al.
Italian Journal of Pediatrics|February 22, 2025
KBG syndrome: report and follow-up on three unrelated patients observed at different agesGregorio Serra, Pierandrea Elefante, Ylenia Gazzitano, et al.
Pageof 7