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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 15, 2021
Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study
Giacomo Garone, Valentina Ferro, Marta Barbato, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2015
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region
Francesco Nicita, Giacomo Garone, Alberto Spalice, et al.
Italian Journal of Pediatrics
|
April 24, 2024
Pediatric torticollis: clinical report and predictors of urgency of 1409 cases
Umberto Raucci, Marco Roversi, Alessandro Ferretti, et al.
Children (Basel, Switzerland)
|
November 25, 2023
Acute Pupillary Disorders in Children: A 10-Year Retrospective Study of 101 Patients
Giacomo Garone, Marco Roversi, Mara Pisani, et al.
BMC Psychiatry
|
February 25, 2025
Understanding and targeting repetitive behaviors and restricted interests in autism spectrum disorder via high-definition transcranial direct current stimulation: a study-protocol
Giulia Lazzaro, Sara Passarini, Andrea Battisti, et al.
Frontiers in Neurology
|
March 2, 2026
The role of pallidotomy in the precision medicine era
Giacomo Garone, Alice Innocenti, Alessandro De Benedictis, et al.
Journal of Personalized Medicine
|
January 21, 2022
"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats
Federica Graziola, Sabrina Maffi, Melissa Grasso, et al.
Pediatric Neurology
|
December 15, 2019
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations
Sabina Barresi, Maria Lisa Dentici, Francesca Manzoni, et al.
Parkinsonism & Related Disorders
|
January 16, 2019
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review
Tommaso Schirinzi, Giacomo Garone, Lorena Travaglini, et al.
Genes
|
April 27, 2024
Spectrum of <i>ERCC6</i>-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, et al.
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Search research articles
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Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 15, 2021
Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study
Giacomo Garone, Valentina Ferro, Marta Barbato, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2015
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region
Francesco Nicita, Giacomo Garone, Alberto Spalice, et al.
Italian Journal of Pediatrics
|
April 24, 2024
Pediatric torticollis: clinical report and predictors of urgency of 1409 cases
Umberto Raucci, Marco Roversi, Alessandro Ferretti, et al.
Children (Basel, Switzerland)
|
November 25, 2023
Acute Pupillary Disorders in Children: A 10-Year Retrospective Study of 101 Patients
Giacomo Garone, Marco Roversi, Mara Pisani, et al.
BMC Psychiatry
|
February 25, 2025
Understanding and targeting repetitive behaviors and restricted interests in autism spectrum disorder via high-definition transcranial direct current stimulation: a study-protocol
Giulia Lazzaro, Sara Passarini, Andrea Battisti, et al.
Frontiers in Neurology
|
March 2, 2026
The role of pallidotomy in the precision medicine era
Giacomo Garone, Alice Innocenti, Alessandro De Benedictis, et al.
Journal of Personalized Medicine
|
January 21, 2022
"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats
Federica Graziola, Sabrina Maffi, Melissa Grasso, et al.
Pediatric Neurology
|
December 15, 2019
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations
Sabina Barresi, Maria Lisa Dentici, Francesca Manzoni, et al.
Parkinsonism & Related Disorders
|
January 16, 2019
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review
Tommaso Schirinzi, Giacomo Garone, Lorena Travaglini, et al.
Genes
|
April 27, 2024
Spectrum of <i>ERCC6</i>-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, et al.
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of 5