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Neurology. Genetics

Showing results (771-780 of 842) with videos related to

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Neurology. Genetics|March 18, 2021
Novel Mutation m.10372A>G in <i>MT-ND3</i> Causing Sensorimotor Axonal PolyneuropathyHelene Bruhn, Kristin Samuelsson, Florian A Schober, et al.
Neurology. Genetics|May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.
Neurology. Genetics|August 16, 2018
Axon reflex-mediated vasodilation is reduced in proportion to disease severity in TTR-FAPIrène Calero-Romero, Marc R Suter, Bernard Waeber, et al.
Neurology. Genetics|August 16, 2018
Association study between multiple system atrophy and TREM2 p.R47HKotaro Ogaki, Michael G Heckman, Shunsuke Koga, et al.
Neurology. Genetics|November 21, 2022
Relationships of <i>APOE</i> Genotypes With Small RNA and Protein Cargo of Brain Tissue Extracellular Vesicles From Patients With Late-Stage ADYiyao Huang, Tom A P Driedonks, Lesley Cheng, et al.
Neurology. Genetics|November 16, 2022
Cognitive Impairment in a Complex Family With AAGGG and ACAGG Repeat Expansions in RFC1 Detected by ExpansionHunter DenovoKazuki Watanabe, Mitsuko Nakashima, Rie Wakatsuki, et al.
Neurology. Genetics|August 15, 2022
A Fast and Robust Strategy to Remove Variant-Level Artifacts in Alzheimer Disease Sequencing Project DataMichael E Belloy, Yann Le Guen, Sarah J Eger, et al.
Neurology. Genetics|February 25, 2025
Involvement of the Superior Cerebellar Peduncles in GAA-<i>FGF14</i> AtaxiaShihan Chen, Catherine Ashton, Rawan Sakalla, et al.
Neurology. Genetics|January 28, 2025
Spinocerebellar Ataxia Type 2: A Review and Personal PerspectiveStefan M Pulst
Neurology. Genetics|November 18, 2024
TRPM8 Mutations Associated With Persistent Pain After Surgical Injury of Corneal Trigeminal AxonsMohammad-Reza Ghovanloo, Philip R Effraim, Sidharth Tyagi, et al.
Pageof 85

Showing results (771-780 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|March 18, 2021
Novel Mutation m.10372A>G in <i>MT-ND3</i> Causing Sensorimotor Axonal PolyneuropathyHelene Bruhn, Kristin Samuelsson, Florian A Schober, et al.
Neurology. Genetics|May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.
Neurology. Genetics|August 16, 2018
Axon reflex-mediated vasodilation is reduced in proportion to disease severity in TTR-FAPIrène Calero-Romero, Marc R Suter, Bernard Waeber, et al.
Neurology. Genetics|August 16, 2018
Association study between multiple system atrophy and TREM2 p.R47HKotaro Ogaki, Michael G Heckman, Shunsuke Koga, et al.
Neurology. Genetics|November 21, 2022
Relationships of <i>APOE</i> Genotypes With Small RNA and Protein Cargo of Brain Tissue Extracellular Vesicles From Patients With Late-Stage ADYiyao Huang, Tom A P Driedonks, Lesley Cheng, et al.
Neurology. Genetics|November 16, 2022
Cognitive Impairment in a Complex Family With AAGGG and ACAGG Repeat Expansions in RFC1 Detected by ExpansionHunter DenovoKazuki Watanabe, Mitsuko Nakashima, Rie Wakatsuki, et al.
Neurology. Genetics|August 15, 2022
A Fast and Robust Strategy to Remove Variant-Level Artifacts in Alzheimer Disease Sequencing Project DataMichael E Belloy, Yann Le Guen, Sarah J Eger, et al.
Neurology. Genetics|February 25, 2025
Involvement of the Superior Cerebellar Peduncles in GAA-<i>FGF14</i> AtaxiaShihan Chen, Catherine Ashton, Rawan Sakalla, et al.
Neurology. Genetics|January 28, 2025
Spinocerebellar Ataxia Type 2: A Review and Personal PerspectiveStefan M Pulst
Neurology. Genetics|November 18, 2024
TRPM8 Mutations Associated With Persistent Pain After Surgical Injury of Corneal Trigeminal AxonsMohammad-Reza Ghovanloo, Philip R Effraim, Sidharth Tyagi, et al.
Pageof 85