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Neurology. Genetics

Showing results (791-800 of 842) with videos related to

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Neurology. Genetics|May 8, 2024
Large-Scale Whole-Genome Analysis of HTLV-1-Associated Myelopathy Identified Hereditary Spastic ParaplegiasNaoki Takao, Naoko Yagishita, Natsumi Araya, et al.
Neurology. Genetics|April 30, 2024
Erratum: Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
Neurology. Genetics|June 6, 2024
Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic ParaplegiaZhi-Xian Ye, Hao-Ling Xu, Na-Ping Chen, et al.
Neurology. Genetics|May 31, 2024
Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple SclerosisElina Misicka, Yunfeng Huang, Stephanie Loomis, et al.
Neurology. Genetics|May 10, 2024
Homozygosity of a Founder Variant c.1508dupC in <i>DOK7</i> Causes Congenital Myasthenia With Variable SeverityJohanna Palmio, Panu Kiviranta, Päivi H Hartikainen, et al.
Neurology. Genetics|May 8, 2024
Cerebellar Micro-RNA Profile in a Mouse Model of Spinocerebellar Ataxia Type 2Sharan Paul, Warunee Dansithong, Mandi Gandelman, et al.
Neurology. Genetics|May 8, 2024
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic <i>GRIN2A</i> VariantsDaisy G Y Thompson-Lake, Frederique J Liegeois, Ruth O Braden, et al.
Neurology. Genetics|May 28, 2024
Erratum: Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Neurology. Genetics|April 15, 2024
Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical TestingSonya Watson, Kathie J Ngo, Hannah A Stevens, et al.
Neurology. Genetics|January 19, 2026
Autosomal Dominant <i>FTH1</i> Variant Causing Pontocerebellar Hypoplasia and Late-Onset Neuroferritinopathy: A Case ReportJasmijn Annemiek Hebbink, Jikke-Mien F Niermeijer, Elene Vroegindeweij, et al.
Pageof 85

Showing results (791-800 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|May 8, 2024
Large-Scale Whole-Genome Analysis of HTLV-1-Associated Myelopathy Identified Hereditary Spastic ParaplegiasNaoki Takao, Naoko Yagishita, Natsumi Araya, et al.
Neurology. Genetics|April 30, 2024
Erratum: Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
Neurology. Genetics|June 6, 2024
Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic ParaplegiaZhi-Xian Ye, Hao-Ling Xu, Na-Ping Chen, et al.
Neurology. Genetics|May 31, 2024
Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple SclerosisElina Misicka, Yunfeng Huang, Stephanie Loomis, et al.
Neurology. Genetics|May 10, 2024
Homozygosity of a Founder Variant c.1508dupC in <i>DOK7</i> Causes Congenital Myasthenia With Variable SeverityJohanna Palmio, Panu Kiviranta, Päivi H Hartikainen, et al.
Neurology. Genetics|May 8, 2024
Cerebellar Micro-RNA Profile in a Mouse Model of Spinocerebellar Ataxia Type 2Sharan Paul, Warunee Dansithong, Mandi Gandelman, et al.
Neurology. Genetics|May 8, 2024
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic <i>GRIN2A</i> VariantsDaisy G Y Thompson-Lake, Frederique J Liegeois, Ruth O Braden, et al.
Neurology. Genetics|May 28, 2024
Erratum: Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Neurology. Genetics|April 15, 2024
Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical TestingSonya Watson, Kathie J Ngo, Hannah A Stevens, et al.
Neurology. Genetics|January 19, 2026
Autosomal Dominant <i>FTH1</i> Variant Causing Pontocerebellar Hypoplasia and Late-Onset Neuroferritinopathy: A Case ReportJasmijn Annemiek Hebbink, Jikke-Mien F Niermeijer, Elene Vroegindeweij, et al.
Pageof 85