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Neurology. Genetics

Showing results (371-380 of 1,012) with videos related to

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Neurology. Genetics|March 19, 2020
Heritability of cervical spinal cord structureLinda Solstrand Dahlberg, Olivia Viessmann, Clas Linnman
Neurology. Genetics|March 20, 2020
Differential subcellular expression of <sup>P525L</sup>FUS as a putative biomarker for ALS phenoconversionMaria Caputo, Vincenzo La Bella, Antonietta Notaro
Neurology. Genetics|December 25, 2019
Headaches and polygenic scoresBjarni J Vilhjálmsson, Florian Privé
Neurology. Genetics|March 27, 2020
Heterozygous <i>STUB1</i> missense variants cause ataxia, cognitive decline, and STUB1 mislocalizationDong-Hui Chen, Caitlin Latimer, Mayumi Yagi, et al.
Neurology. Genetics|October 16, 2020
Rapid progressive ALS in a patient with a <i>DNAJC7</i> loss-of-function mutationKang-Yang Jih, Pei-Chien Tsai, Yu-Shuen Tsai, et al.
Neurology. Genetics|August 28, 2020
Variant repeats within the <i>DMPK</i> CTG expansion protect function in myotonic dystrophy type 1Jacob N Miller, Ellen van der Plas, Mark Hamilton, et al.
Neurology. Genetics|December 28, 2018
Erratum: Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)
Neurology. Genetics|November 23, 2020
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?Christiane Reitz, Ekaterina Rogaeva, Gary W Beecham
Neurology. Genetics|August 14, 2024
MRI Insights in Hypomyelinating Disorders With Early Myelination DisturbancesPrateek Malik, Bidkar Sayli U, Benjamin B Mathew, et al.
Neurology. Genetics|July 11, 2022
FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic InheritanceOrly Goldstein, Talya Inbar, Merav Kedmi, et al.
Pageof 102

Showing results (371-380 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|March 19, 2020
Heritability of cervical spinal cord structureLinda Solstrand Dahlberg, Olivia Viessmann, Clas Linnman
Neurology. Genetics|March 20, 2020
Differential subcellular expression of <sup>P525L</sup>FUS as a putative biomarker for ALS phenoconversionMaria Caputo, Vincenzo La Bella, Antonietta Notaro
Neurology. Genetics|December 25, 2019
Headaches and polygenic scoresBjarni J Vilhjálmsson, Florian Privé
Neurology. Genetics|March 27, 2020
Heterozygous <i>STUB1</i> missense variants cause ataxia, cognitive decline, and STUB1 mislocalizationDong-Hui Chen, Caitlin Latimer, Mayumi Yagi, et al.
Neurology. Genetics|October 16, 2020
Rapid progressive ALS in a patient with a <i>DNAJC7</i> loss-of-function mutationKang-Yang Jih, Pei-Chien Tsai, Yu-Shuen Tsai, et al.
Neurology. Genetics|August 28, 2020
Variant repeats within the <i>DMPK</i> CTG expansion protect function in myotonic dystrophy type 1Jacob N Miller, Ellen van der Plas, Mark Hamilton, et al.
Neurology. Genetics|December 28, 2018
Erratum: Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)
Neurology. Genetics|November 23, 2020
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?Christiane Reitz, Ekaterina Rogaeva, Gary W Beecham
Neurology. Genetics|August 14, 2024
MRI Insights in Hypomyelinating Disorders With Early Myelination DisturbancesPrateek Malik, Bidkar Sayli U, Benjamin B Mathew, et al.
Neurology. Genetics|July 11, 2022
FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic InheritanceOrly Goldstein, Talya Inbar, Merav Kedmi, et al.
Pageof 102