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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center study
Vito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions
|
August 26, 2023
Aspiration thrombectomy of M2 segment in acute ischemic stroke: The clinical reality in a neurovascular reference center
Marco Nezzo, Gianluca Cecchi, Francesco Nicita, 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.
Cerebellum (London, England)
|
February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations
Tommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
Italian Journal of Pediatrics
|
June 22, 2012
WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features
Anna Maria Zicari, Luigi Tarani, Daniela Perotti, et al.
Current Neuropharmacology
|
December 2, 2010
Clinical and pharmacological aspects of inflammatory demyelinating diseases in childhood: an update
Alberto Spalice, Pasquale Parisi, Laura Papetti, 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.
Neuromuscular Disorders : NMD
|
August 11, 2022
Neuropsychological and behavioral profile in a cohort of Becker muscular dystrophy pediatric patients
Francesca Cumbo, Michele Tosi, Michela Catteruccia, et al.
International Journal of Molecular Sciences
|
February 23, 2020
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics
Antonella Sferra, Stefania Petrini, Emanuele Bellacchio, et al.
Clinical Neurology and Neurosurgery
|
March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia
Giulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
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Search research articles
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Showing results (41-50 of 120) with videos related to
Sort By:
Page
of 12
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center study
Vito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions
|
August 26, 2023
Aspiration thrombectomy of M2 segment in acute ischemic stroke: The clinical reality in a neurovascular reference center
Marco Nezzo, Gianluca Cecchi, Francesco Nicita, 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.
Cerebellum (London, England)
|
February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations
Tommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
Italian Journal of Pediatrics
|
June 22, 2012
WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features
Anna Maria Zicari, Luigi Tarani, Daniela Perotti, et al.
Current Neuropharmacology
|
December 2, 2010
Clinical and pharmacological aspects of inflammatory demyelinating diseases in childhood: an update
Alberto Spalice, Pasquale Parisi, Laura Papetti, 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.
Neuromuscular Disorders : NMD
|
August 11, 2022
Neuropsychological and behavioral profile in a cohort of Becker muscular dystrophy pediatric patients
Francesca Cumbo, Michele Tosi, Michela Catteruccia, et al.
International Journal of Molecular Sciences
|
February 23, 2020
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics
Antonella Sferra, Stefania Petrini, Emanuele Bellacchio, et al.
Clinical Neurology and Neurosurgery
|
March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia
Giulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
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of 12