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Davide Vecchio

Showing results (1-10 of 46) with videos related to

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The Journal of Pediatrics|June 29, 2016
The Coat-Hanger Angle SignDavide Vecchio, Mario Giuffrè
The Journal of Pediatrics|September 28, 2014
An unusual oral swellingDavide Vecchio, Giovanni Corsello
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Green nail syndromeGiovanni Corsello, Davide Vecchio
Epilepsy & Behavior : E&B|September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosomeMaria Piccione, Davide Vecchio, Emanuela Salzano, et al.
Pediatric Research|February 3, 2021
Ancient Romans and Down SyndromeDavide Vecchio, Marina Macchiaiolo, Michaela Veronika Gonfiantini, et al.
Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplicationMaria Piccione, Davide Vecchio, Simona Cavani, et al.
Frontiers in Genetics|January 8, 2024
Commentary: Case report: Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) presenting with liver cirrhosis and steroid-responsive interstitial pneumoniaFilippo M Panfili, Andrea Pietrobattista, Davide Vecchio, et al.
American Journal of Medical Genetics. Part A|May 13, 2026
Unusual Head and Neck Vascular Patterns in Two Patients With Cornelia de Lange Syndrome: A Case-Based Insight Into Cerebrovascular AnomaliesMarina Macchiaiolo, Alessia Carboni, Michaela Veronika Gonfiantini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2015
4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterizationMaria Piccione, Emanuela Salzano, Davide Vecchio, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|June 29, 2016
The Coat-Hanger Angle SignDavide Vecchio, Mario Giuffrè
The Journal of Pediatrics|September 28, 2014
An unusual oral swellingDavide Vecchio, Giovanni Corsello
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Green nail syndromeGiovanni Corsello, Davide Vecchio
Epilepsy & Behavior : E&B|September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosomeMaria Piccione, Davide Vecchio, Emanuela Salzano, et al.
Pediatric Research|February 3, 2021
Ancient Romans and Down SyndromeDavide Vecchio, Marina Macchiaiolo, Michaela Veronika Gonfiantini, et al.
Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplicationMaria Piccione, Davide Vecchio, Simona Cavani, et al.
Frontiers in Genetics|January 8, 2024
Commentary: Case report: Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) presenting with liver cirrhosis and steroid-responsive interstitial pneumoniaFilippo M Panfili, Andrea Pietrobattista, Davide Vecchio, et al.
American Journal of Medical Genetics. Part A|May 13, 2026
Unusual Head and Neck Vascular Patterns in Two Patients With Cornelia de Lange Syndrome: A Case-Based Insight Into Cerebrovascular AnomaliesMarina Macchiaiolo, Alessia Carboni, Michaela Veronika Gonfiantini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2015
4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterizationMaria Piccione, Emanuela Salzano, Davide Vecchio, et al.
Pageof 5