Ennio Del Giudice

Naples, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 38 publications

Sleep disruption and neuropsychiatric features in Angelman syndrome: insights into underlying neurobiology.

Sleep disruption and neuropsychiatric features in Angelman syndrome: insights into underlying neurobiology.

Journal: Sleep medicine

Published: April 27, 2026

Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements.

Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements.

Journal: Journal of clinical medicine

Published: January 13, 2024

Electroencephalographic findings in ATRX syndrome: A new case series and review of literature.

Electroencephalographic findings in ATRX syndrome: A new case series and review of literature.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: April 05, 2022

Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications.

Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: September 14, 2021

Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy.

Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: April 06, 2020

A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome.

A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome.

Journal: Seizure

Published: February 18, 2020

A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.

A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.

Journal: Clinical genetics

Published: February 17, 2020

Expansion of the phenotype of lateral meningocele syndrome.

Expansion of the phenotype of lateral meningocele syndrome.

Journal: American journal of medical genetics. Part A

Published: November 20, 2019

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.

Journal: Epilepsy & behavior : E&B

Published: July 15, 2019

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.

Journal: American journal of human genetics

Published: July 02, 2019

Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment.

Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment.

Journal: Minerva pediatrics

Published: May 28, 2019

Epilepsy in Rett Syndrome: can seizures play an encephalopathic effect in this disorder?

Epilepsy in Rett Syndrome: can seizures play an encephalopathic effect in this disorder?

Journal: Minerva pediatrica

Published: April 10, 2019

Showing 1-12 of 38

Last Updated: 09/26/2026