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Giacomo Garone

Showing results (1-10 of 41) with videos related to

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The Application of Clinical Genetics|April 14, 2020
Alternating Hemiplegia of Childhood: Understanding the Genotype-Phenotype Relationship of ATP1A3 VariationsAlessandro Capuano, Giacomo Garone, Giuseppe Tiralongo, et al.
Journal of Clinical Medicine|July 2, 2021
Acute Movement Disorders in ChildhoodGiacomo Garone, Federica Graziola, Melissa Grasso, et al.
Journal of Clinical Medicine|August 27, 2021
Cognitive Assessment in <i>GNAO1</i> Neurodevelopmental Disorder Using an Eye Tracking SystemFederica Graziola, Giacomo Garone, Melissa Grasso, et al.
Parkinsonism & Related Disorders|June 6, 2021
Working memory, attention and planning abilities in NKX2.1-related choreaFederica Graziola, Giacomo Garone, Melissa Grasso, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Parkinsonism & Related Disorders|February 26, 2025
RHOBTB2-related paroxysmal hemiparesis: From alternating hemiplegia to hemiplegic migraineAlice Innocenti, Giacomo Garone, Laura Papetti, et al.
Epilepsy & Behavior : E&B|July 23, 2018
Could Rolandic spikes be a prognostic factor of the neurocognitive outcome of children with BECTS?Isabella Tristano, Francesco Nicita, Giacomo Garone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2025
Biallelic Variants in SLC27A3 Cause a Complex Form of Neurodegeneration with Brain Iron AccumulationLorena Travaglini, Cherim Jeon, Teresa Rizza, et al.
Metabolic Brain Disease|July 22, 2015
Severe early onset ethylmalonic encephalopathy with West syndromeLaura Papetti, Giacomo Garone, Livia Schettini, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
The Application of Clinical Genetics|April 14, 2020
Alternating Hemiplegia of Childhood: Understanding the Genotype-Phenotype Relationship of ATP1A3 VariationsAlessandro Capuano, Giacomo Garone, Giuseppe Tiralongo, et al.
Journal of Clinical Medicine|July 2, 2021
Acute Movement Disorders in ChildhoodGiacomo Garone, Federica Graziola, Melissa Grasso, et al.
Journal of Clinical Medicine|August 27, 2021
Cognitive Assessment in <i>GNAO1</i> Neurodevelopmental Disorder Using an Eye Tracking SystemFederica Graziola, Giacomo Garone, Melissa Grasso, et al.
Parkinsonism & Related Disorders|June 6, 2021
Working memory, attention and planning abilities in NKX2.1-related choreaFederica Graziola, Giacomo Garone, Melissa Grasso, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Parkinsonism & Related Disorders|February 26, 2025
RHOBTB2-related paroxysmal hemiparesis: From alternating hemiplegia to hemiplegic migraineAlice Innocenti, Giacomo Garone, Laura Papetti, et al.
Epilepsy & Behavior : E&B|July 23, 2018
Could Rolandic spikes be a prognostic factor of the neurocognitive outcome of children with BECTS?Isabella Tristano, Francesco Nicita, Giacomo Garone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2025
Biallelic Variants in SLC27A3 Cause a Complex Form of Neurodegeneration with Brain Iron AccumulationLorena Travaglini, Cherim Jeon, Teresa Rizza, et al.
Metabolic Brain Disease|July 22, 2015
Severe early onset ethylmalonic encephalopathy with West syndromeLaura Papetti, Giacomo Garone, Livia Schettini, et al.
Pageof 5