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Ettore Piro

Showing results (31-40 of 70) with videos related to

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Critical Care Research and Practice|August 24, 2021
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter ProjectRaffaele Falsaperla, Laura Mauceri, Milena Motta, et al.
Italian Journal of Pediatrics|September 7, 2023
Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonologyCarlo Caffarelli, Francesca Santamaria, Ettore Piro, et al.
Italian Journal of Pediatrics|April 6, 2018
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1Giovanni Corsello, Vincenzo Antona, Gregorio Serra, et al.
Italian Journal of Pediatrics|July 29, 2022
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorderIngrid Anne Mandy Schierz, Salvatore Amoroso, Vincenzo Antona, et al.
Italian Journal of Pediatrics|July 29, 2022
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 geneGregorio Serra, Vincenzo Antona, Chiara Cannata, et al.
Italian Journal of Pediatrics|November 26, 2022
New insights in pediatrics in 2021: choices in allergy and immunology, critical care, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, neurology, nutrition, palliative care, respiratory tract illnesses and telemedicineCarlo Caffarelli, Francesca Santamaria, Ettore Piro, et al.
American Journal of Medical Genetics. Part A|November 10, 2005
Perlman syndrome: clinical report and nine-year follow-upMaria Piccione, Massimiliano Cecconi, Mario Giuffrè, et al.
Italian Journal of Pediatrics|September 19, 2020
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutationEttore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
Italian Journal of Pediatrics|September 19, 2020
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case reportIngrid Anne Mandy Schierz, Marcello Cimador, Mario Giuffrè, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 21, 2019
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcomeEttore Piro, Rosaria Nardello, Elena Gennaro, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Critical Care Research and Practice|August 24, 2021
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter ProjectRaffaele Falsaperla, Laura Mauceri, Milena Motta, et al.
Italian Journal of Pediatrics|September 7, 2023
Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonologyCarlo Caffarelli, Francesca Santamaria, Ettore Piro, et al.
Italian Journal of Pediatrics|April 6, 2018
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1Giovanni Corsello, Vincenzo Antona, Gregorio Serra, et al.
Italian Journal of Pediatrics|July 29, 2022
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorderIngrid Anne Mandy Schierz, Salvatore Amoroso, Vincenzo Antona, et al.
Italian Journal of Pediatrics|July 29, 2022
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 geneGregorio Serra, Vincenzo Antona, Chiara Cannata, et al.
Italian Journal of Pediatrics|November 26, 2022
New insights in pediatrics in 2021: choices in allergy and immunology, critical care, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, neurology, nutrition, palliative care, respiratory tract illnesses and telemedicineCarlo Caffarelli, Francesca Santamaria, Ettore Piro, et al.
American Journal of Medical Genetics. Part A|November 10, 2005
Perlman syndrome: clinical report and nine-year follow-upMaria Piccione, Massimiliano Cecconi, Mario Giuffrè, et al.
Italian Journal of Pediatrics|September 19, 2020
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutationEttore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
Italian Journal of Pediatrics|September 19, 2020
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case reportIngrid Anne Mandy Schierz, Marcello Cimador, Mario Giuffrè, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 21, 2019
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcomeEttore Piro, Rosaria Nardello, Elena Gennaro, et al.
Pageof 7