Giacomo Garone | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Pediatric torticollis: clinical report and predictors of urgency of 1409 cases	THE ITALIAN JOURNAL OF PEDIATRICS	2024
Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies	NEUROLOGY	2023
Acute Pupillary Disorders in Children: A 10-Year Retrospective Study of 101 Patients	CHILDREN	2023
“Spazio Huntington”: Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats	JOURNAL OF PERSONALIZED MEDICINE	2022
“Spazio Huntington”: Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats	JOURNAL OF PERSONALIZED MEDICINE	2022
Highlighting the Dystonic Phenotype Related to GNAO1	MOVEMENT DISORDERS	2022
Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study	EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY	2021
Cognitive deficits in children with brain tumours: A project to create a software for cognitive training	Abstracts from the World Congress of Neurology (WCN 2021)JOURNAL OF THE NEUROLOGICAL SCIENCES	2021
Acute movement disorders in childhood	JOURNAL OF CLINICAL MEDICINE	2021
Cognitive assessment in GNAO1 neurodevelopmental disorder using an eye tracking system	JOURNAL OF CLINICAL MEDICINE	2021
Working memory, attention and planning abilities in NKX2.1-related chorea	PARKINSONISM & RELATED DISORDERS	2021
Characteristics of acute nystagmus in the pediatric emergency department	PEDIATRICS	2020
Impact of Italian lockdown on Tourette's syndrome patients at the time of the COVID-19 pandemic	PSYCHIATRY AND CLINICAL NEUROSCIENCES	2020
Clinical and genetic overview of paroxysmal movement disorders and episodic ataxias	INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES	2020
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations	PEDIATRIC NEUROLOGY	2020
Prestatus and status dystonicus in children and adolescents	DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY	2020
Alternating hemiplegia of childhood: Understanding the genotype–phenotype relationship of ATP1A3 variations	THE APPLICATION OF CLINICAL GENETICS	2020
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review	PARKINSONISM & RELATED DISORDERS	2019
Acute ataxia in paediatric emergency departments: a multicentre Italian study	ARCHIVES OF DISEASE IN CHILDHOOD	2019
Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study	FRONTIERS IN GENETICS	2019