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JAMA Neurology
|
August 29, 2022
Efficacy and Safety of Vamorolone vs Placebo and Prednisone Among Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial
Michela Guglieri, Paula R Clemens, Seth J Perlman, et al.
Neurology
|
December 5, 2020
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome
Silvia Masnada, Anna Pichiecchio, Manuela Formica, et al.
American Journal of Human Genetics
|
April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Brain : a Journal of Neurology
|
September 3, 2020
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
Jorge Alonso-Pérez, Lidia González-Quereda, Luca Bello, et al.
Brain : a Journal of Neurology
|
October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond
Carla Marini, Alessandro Porro, Agnès Rastetter, et al.
Annals of Neurology
|
January 24, 2025
Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Sandra Coppens, Nicolas Deconinck, Patricia Sullivan, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Annals of Neurology
|
April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
Emily C Oates, Kristi J Jones, Sandra Donkervoort, et al.
Nature Genetics
|
October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
JAMA Neurology
|
August 29, 2022
Efficacy and Safety of Vamorolone vs Placebo and Prednisone Among Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial
Michela Guglieri, Paula R Clemens, Seth J Perlman, et al.
Neurology
|
December 5, 2020
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome
Silvia Masnada, Anna Pichiecchio, Manuela Formica, et al.
American Journal of Human Genetics
|
April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Brain : a Journal of Neurology
|
September 3, 2020
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
Jorge Alonso-Pérez, Lidia González-Quereda, Luca Bello, et al.
Brain : a Journal of Neurology
|
October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond
Carla Marini, Alessandro Porro, Agnès Rastetter, et al.
Annals of Neurology
|
January 24, 2025
Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Sandra Coppens, Nicolas Deconinck, Patricia Sullivan, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Annals of Neurology
|
April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
Emily C Oates, Kristi J Jones, Sandra Donkervoort, et al.
Nature Genetics
|
October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
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of 8