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Alessandro Capuano

Showing results (41-50 of 71) 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.
Neuroscience Research|July 9, 2013
Different SEP recovery cycle in adolescent migraineurs with exploding or imploding painElisa Iacovelli, Samuela Tarantino, Alessandro Capuano, et al.
Parkinsonism & Related Disorders|June 9, 2016
Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrumFrancesco Nicita, Lorena Travaglini, Sandro Sabatini, 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.
Parkinsonism & Related Disorders|December 24, 2018
A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorderFederica Graziola, Fabrizia Stregapede, Lorena Travaglini, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, 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.
The Journal of Headache and Pain|May 9, 2013
Clinical features, anger management and anxiety: a possible correlation in migraine childrenSamuela Tarantino, Cristiana De Ranieri, Cecilia Dionisi, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
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.
Neuroscience Research|July 9, 2013
Different SEP recovery cycle in adolescent migraineurs with exploding or imploding painElisa Iacovelli, Samuela Tarantino, Alessandro Capuano, et al.
Parkinsonism & Related Disorders|June 9, 2016
Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrumFrancesco Nicita, Lorena Travaglini, Sandro Sabatini, 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.
Parkinsonism & Related Disorders|December 24, 2018
A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorderFederica Graziola, Fabrizia Stregapede, Lorena Travaglini, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, 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.
The Journal of Headache and Pain|May 9, 2013
Clinical features, anger management and anxiety: a possible correlation in migraine childrenSamuela Tarantino, Cristiana De Ranieri, Cecilia Dionisi, et al.
Pageof 8