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Frontiers in Genetics
|
November 19, 2019
Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study
Federica Graziola, Giacomo Garone, Fabrizia Stregapede, et al.
International Journal of Molecular Sciences
|
May 24, 2020
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
Brain Sciences
|
February 26, 2025
Three Cases of Spinocerebellar Ataxia Type 2 (SCA2) and Pediatric Literature Review: Do Not Forget Trinucleotide Repeat Disorders in Childhood-Onset Progressive Ataxia
Jacopo Sartorelli, Maria Grazia Pomponi, Giacomo Garone, et al.
Developmental Medicine and Child Neurology
|
December 15, 2019
Prestatus and status dystonicus in children and adolescents
Giacomo Garone, Federica Graziola, Francesco Nicita, et al.
Italian Journal of Pediatrics
|
May 31, 2018
A cohort study on acute ocular motility disorders in pediatric emergency department
Umberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Frontiers in Pediatrics
|
January 29, 2024
Case Report: A rare form of congenital erythrocytosis due to <i>SLC30A10</i> biallelic variants-differential diagnosis and recommendation for biochemical and genetic screening
Rosalinda Giannini, Emanuele Agolini, Giuseppe Palumbo, et al.
Clinical Toxicology (Philadelphia, Pa.)
|
August 6, 2025
Neurological features of acute poisoning in paediatric patients presenting to the emergency department: a retrospective study
Marco Roversi, Marco Marano, Francesca Cautilli, et al.
Neuropediatrics
|
February 6, 2025
Congenital Ataxia with Progressive Cerebellar Atrophy, Camptodactyly, and Hypertrichosis: A Novel Recognizable Phenotype for NALCN Heterozygous Variants
Jacopo Sartorelli, Lorena Travaglini, Giacomo Garone, et al.
Parkinsonism & Related Disorders
|
January 8, 2025
Segmental brainstem myoclonus in ADCK3-Related ataxia: A novel phenomenon?
Vito Luigi Colona, Giacomo Garone, Francesco Nicita, et al.
Neurology
|
September 25, 2023
Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies
Sterre van der Veen, Gabrielle T W Tse, Alessandro Ferretti, et al.
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Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Frontiers in Genetics
|
November 19, 2019
Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study
Federica Graziola, Giacomo Garone, Fabrizia Stregapede, et al.
International Journal of Molecular Sciences
|
May 24, 2020
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
Brain Sciences
|
February 26, 2025
Three Cases of Spinocerebellar Ataxia Type 2 (SCA2) and Pediatric Literature Review: Do Not Forget Trinucleotide Repeat Disorders in Childhood-Onset Progressive Ataxia
Jacopo Sartorelli, Maria Grazia Pomponi, Giacomo Garone, et al.
Developmental Medicine and Child Neurology
|
December 15, 2019
Prestatus and status dystonicus in children and adolescents
Giacomo Garone, Federica Graziola, Francesco Nicita, et al.
Italian Journal of Pediatrics
|
May 31, 2018
A cohort study on acute ocular motility disorders in pediatric emergency department
Umberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Frontiers in Pediatrics
|
January 29, 2024
Case Report: A rare form of congenital erythrocytosis due to <i>SLC30A10</i> biallelic variants-differential diagnosis and recommendation for biochemical and genetic screening
Rosalinda Giannini, Emanuele Agolini, Giuseppe Palumbo, et al.
Clinical Toxicology (Philadelphia, Pa.)
|
August 6, 2025
Neurological features of acute poisoning in paediatric patients presenting to the emergency department: a retrospective study
Marco Roversi, Marco Marano, Francesca Cautilli, et al.
Neuropediatrics
|
February 6, 2025
Congenital Ataxia with Progressive Cerebellar Atrophy, Camptodactyly, and Hypertrichosis: A Novel Recognizable Phenotype for NALCN Heterozygous Variants
Jacopo Sartorelli, Lorena Travaglini, Giacomo Garone, et al.
Parkinsonism & Related Disorders
|
January 8, 2025
Segmental brainstem myoclonus in ADCK3-Related ataxia: A novel phenomenon?
Vito Luigi Colona, Giacomo Garone, Francesco Nicita, et al.
Neurology
|
September 25, 2023
Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies
Sterre van der Veen, Gabrielle T W Tse, Alessandro Ferretti, et al.
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of 5