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Federica Graziola

Showing results (11-20 of 28) with videos related to

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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 StudyFederica 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 AtaxiasGiacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
Frontiers in Neurology|September 5, 2025
Preliminary observations of glucose metabolism dysregulation in pediatric Huntington's diseaseFederica Graziola, Federica Rachele Danti, Martina Penzo, et al.
Cerebellum (London, England)|February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 MutationsTommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
Developmental Medicine and Child Neurology|December 15, 2019
Prestatus and status dystonicus in children and adolescentsGiacomo Garone, Federica Graziola, Francesco Nicita, et al.
Clinical Genetics|May 9, 2019
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxiaFrancesco Nicita, Marta Nardella, Emanuele Bellacchio, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, et al.
Frontiers in Neurology|May 11, 2026
Video-EEG polygraphy in the clinical characterization of hyperkinetic movement disorders: a tertiary referral cohortDavide Caputo, Brando Rasori, Roberta Solazzi, et al.
Parkinsonism & Related Disorders|September 10, 2020
Movement disorders in ADAR1 disease: Insights from a comprehensive cohortGiulia Di Lazzaro, Federica Graziola, Andrea Sancesario, et al.
Pituitary|September 10, 2015
Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngiomaValeria Scagliotti, Laura Avagliano, Angelica Gualtieri, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
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 StudyFederica 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 AtaxiasGiacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
Frontiers in Neurology|September 5, 2025
Preliminary observations of glucose metabolism dysregulation in pediatric Huntington's diseaseFederica Graziola, Federica Rachele Danti, Martina Penzo, et al.
Cerebellum (London, England)|February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 MutationsTommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
Developmental Medicine and Child Neurology|December 15, 2019
Prestatus and status dystonicus in children and adolescentsGiacomo Garone, Federica Graziola, Francesco Nicita, et al.
Clinical Genetics|May 9, 2019
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxiaFrancesco Nicita, Marta Nardella, Emanuele Bellacchio, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, et al.
Frontiers in Neurology|May 11, 2026
Video-EEG polygraphy in the clinical characterization of hyperkinetic movement disorders: a tertiary referral cohortDavide Caputo, Brando Rasori, Roberta Solazzi, et al.
Parkinsonism & Related Disorders|September 10, 2020
Movement disorders in ADAR1 disease: Insights from a comprehensive cohortGiulia Di Lazzaro, Federica Graziola, Andrea Sancesario, et al.
Pituitary|September 10, 2015
Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngiomaValeria Scagliotti, Laura Avagliano, Angelica Gualtieri, et al.
Pageof 3