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Neurology. Genetics

Showing results (231-240 of 1,011) with videos related to

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Neurology. Genetics|April 6, 2026
Assessment and Treatment of Cutaneous Neurofibromas in Neurofibromatosis Type 1: A Scoping ReviewHadiya Abdalla Elahmar, Carlos Alberto Soto Rincon, Aaron Drucker, et al.
Neurology. Genetics|April 6, 2026
Post-Traumatic Headache in Children and Genetic Risk of Migraine: An Observational Cohort StudySerena L Orr, Andrew D Hershey, Brad G Kurowski, et al.
Neurology. Genetics|April 17, 2026
Novel <i>VRK1</i> Variants and a Founder Effect in Axonal PolyneuropathyKe Xu, Sen Zeng, Xiaobo Li, et al.
Neurology. Genetics|April 16, 2026
Prognostic Significance of <i>NOTCH3</i> Small Vessel Disease Staging for the <i>NOTCH3</i> p.R544C VariantYing-Chi Shen, Chih-Hao Chen, Hung-Chieh Chen, et al.
Neurology. Genetics|April 12, 2016
Expanding the ataxia with oculomotor apraxia type 4 phenotypeMartin Paucar, Helena Malmgren, Malcolm Taylor, et al.
Neurology. Genetics|November 26, 2021
A 3.9-Mb Deletion on 2p11.2 Comprising the <i>REEP1</i> Gene Causes Early-Onset Atypical ParkinsonismRaquel Baviera-Muñoz, Dolores Martínez-Rubio, Isabel Sastre-Bataller, et al.
Neurology. Genetics|November 8, 2021
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Impairments Caused by Biallelic <i>SCO2</i> VariantsBenoit Rucheton, Claire Ewenczyk, Pauline Gaignard, et al.
Neurology. Genetics|March 8, 2019
Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophyBruce Nmezi, Elisa Giorgio, Raili Raininko, et al.
Neurology. Genetics|August 13, 2019
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathyAsfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, et al.
Neurology. Genetics|August 13, 2019
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson diseaseJuan I Young, Sathesh K Sivasankaran, Lily Wang, et al.
Pageof 102

Showing results (231-240 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|April 6, 2026
Assessment and Treatment of Cutaneous Neurofibromas in Neurofibromatosis Type 1: A Scoping ReviewHadiya Abdalla Elahmar, Carlos Alberto Soto Rincon, Aaron Drucker, et al.
Neurology. Genetics|April 6, 2026
Post-Traumatic Headache in Children and Genetic Risk of Migraine: An Observational Cohort StudySerena L Orr, Andrew D Hershey, Brad G Kurowski, et al.
Neurology. Genetics|April 17, 2026
Novel <i>VRK1</i> Variants and a Founder Effect in Axonal PolyneuropathyKe Xu, Sen Zeng, Xiaobo Li, et al.
Neurology. Genetics|April 16, 2026
Prognostic Significance of <i>NOTCH3</i> Small Vessel Disease Staging for the <i>NOTCH3</i> p.R544C VariantYing-Chi Shen, Chih-Hao Chen, Hung-Chieh Chen, et al.
Neurology. Genetics|April 12, 2016
Expanding the ataxia with oculomotor apraxia type 4 phenotypeMartin Paucar, Helena Malmgren, Malcolm Taylor, et al.
Neurology. Genetics|November 26, 2021
A 3.9-Mb Deletion on 2p11.2 Comprising the <i>REEP1</i> Gene Causes Early-Onset Atypical ParkinsonismRaquel Baviera-Muñoz, Dolores Martínez-Rubio, Isabel Sastre-Bataller, et al.
Neurology. Genetics|November 8, 2021
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Impairments Caused by Biallelic <i>SCO2</i> VariantsBenoit Rucheton, Claire Ewenczyk, Pauline Gaignard, et al.
Neurology. Genetics|March 8, 2019
Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophyBruce Nmezi, Elisa Giorgio, Raili Raininko, et al.
Neurology. Genetics|August 13, 2019
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathyAsfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, et al.
Neurology. Genetics|August 13, 2019
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson diseaseJuan I Young, Sathesh K Sivasankaran, Lily Wang, et al.
Pageof 102