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Neurology. Genetics

Showing results (121-130 of 1,011) with videos related to

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Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Neurology. Genetics|March 17, 2021
Detailed Clinical and Psychological Phenotype of the X-linked <i>HNRNPH2</i>-Related Neurodevelopmental DisorderJennifer M Bain, Olivia Thornburg, Cheryl Pan, et al.
Neurology. Genetics|March 10, 2021
Race and Alzheimer Disease Biomarkers: A Neglected RaceAlberto Lleó, Marc Suárez-Calvet
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology. Genetics|December 20, 2021
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic FindingsDianalee McKnight, Sara L Bristow, Rebecca M Truty, et al.
Neurology. Genetics|November 17, 2021
Genetic Predisposition to Mosaic Chromosomal Loss Is Associated With Functional Outcome After Ischemic StrokeMalin Johansson, Annie Pedersen, John W Cole, et al.
Neurology. Genetics|November 29, 2021
Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore SequencingYa Wang, Jianxin Tan, Yan Wang, et al.
Neurology. Genetics|December 13, 2021
Transcript-Specific Loss-of-Function Variants in <i>VPS16</i> Are Enriched in Patients With DystoniaJoohyun Park, Annemarie Reilaender, Jan N Petry-Schmelzer, et al.
Neurology. Genetics|December 9, 2021
Pathogenic <i>NOTCH3</i> Variants Are Frequent Among the Korean General PopulationChul-Hoo Kang, Young Mee Kim, Yang-Ji Kim, et al.
Neurology. Genetics|December 3, 2021
White Matter Hyperintensities and Cerebral Microbleeds in Ataxia-TelangiectasiaMay Yung Tiet, Stefania Nannoni, Daniel Scoffings, et al.
Pageof 102

Showing results (121-130 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Neurology. Genetics|March 17, 2021
Detailed Clinical and Psychological Phenotype of the X-linked <i>HNRNPH2</i>-Related Neurodevelopmental DisorderJennifer M Bain, Olivia Thornburg, Cheryl Pan, et al.
Neurology. Genetics|March 10, 2021
Race and Alzheimer Disease Biomarkers: A Neglected RaceAlberto Lleó, Marc Suárez-Calvet
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology. Genetics|December 20, 2021
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic FindingsDianalee McKnight, Sara L Bristow, Rebecca M Truty, et al.
Neurology. Genetics|November 17, 2021
Genetic Predisposition to Mosaic Chromosomal Loss Is Associated With Functional Outcome After Ischemic StrokeMalin Johansson, Annie Pedersen, John W Cole, et al.
Neurology. Genetics|November 29, 2021
Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore SequencingYa Wang, Jianxin Tan, Yan Wang, et al.
Neurology. Genetics|December 13, 2021
Transcript-Specific Loss-of-Function Variants in <i>VPS16</i> Are Enriched in Patients With DystoniaJoohyun Park, Annemarie Reilaender, Jan N Petry-Schmelzer, et al.
Neurology. Genetics|December 9, 2021
Pathogenic <i>NOTCH3</i> Variants Are Frequent Among the Korean General PopulationChul-Hoo Kang, Young Mee Kim, Yang-Ji Kim, et al.
Neurology. Genetics|December 3, 2021
White Matter Hyperintensities and Cerebral Microbleeds in Ataxia-TelangiectasiaMay Yung Tiet, Stefania Nannoni, Daniel Scoffings, et al.
Pageof 102