Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Neurology. Genetics

Showing results (261-270 of 1,012) with videos related to

Pageof 102
Sort By:
Neurology. Genetics|April 28, 2020
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA<sup>Gly</sup> (<i>MT-TG</i>) variantOlivia V Poole, Alejandro Horga, Steven A Hardy, et al.
Neurology. Genetics|April 28, 2020
Erratum: Heritability of cervical spinal cord structure
Neurology. Genetics|April 28, 2020
Acute encephalopathy after head trauma in a patient with a RHOBTB2 mutationAnnemarie C S Knijnenburg, Joost Nicolai, Levinus A Bok, et al.
Neurology. Genetics|September 3, 2021
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish CohortAyşe Candayan, Arman Çakar, Gulshan Yunisova, et al.
Neurology. Genetics|July 20, 2016
APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhageChia-Ling Phuah, Miriam R Raffeld, Alison M Ayres, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Neurology. Genetics|June 18, 2020
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurology. Genetics|August 19, 2016
Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsySteven A Hardy, Emma L Blakely, Andrew I Purvis, et al.
Neurology. Genetics|September 5, 2025
Vascular NOTCH3 Deposition Load: Association With <i>NOTCH3</i> Genotype and CADASIL Disease SeverityYu-Wen Cheng, Chih-Hao Chen, Chi-Chao Chao, et al.
Neurology. Genetics|May 12, 2021
Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of <i>ATP1A3</i> in Patients Across 3 Global PopulationsKyoko Hoshino, Kathleen J Sweadner, Toshitaka Kawarai, et al.
Pageof 102

Showing results (261-270 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|April 28, 2020
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA<sup>Gly</sup> (<i>MT-TG</i>) variantOlivia V Poole, Alejandro Horga, Steven A Hardy, et al.
Neurology. Genetics|April 28, 2020
Erratum: Heritability of cervical spinal cord structure
Neurology. Genetics|April 28, 2020
Acute encephalopathy after head trauma in a patient with a RHOBTB2 mutationAnnemarie C S Knijnenburg, Joost Nicolai, Levinus A Bok, et al.
Neurology. Genetics|September 3, 2021
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish CohortAyşe Candayan, Arman Çakar, Gulshan Yunisova, et al.
Neurology. Genetics|July 20, 2016
APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhageChia-Ling Phuah, Miriam R Raffeld, Alison M Ayres, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Neurology. Genetics|June 18, 2020
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurology. Genetics|August 19, 2016
Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsySteven A Hardy, Emma L Blakely, Andrew I Purvis, et al.
Neurology. Genetics|September 5, 2025
Vascular NOTCH3 Deposition Load: Association With <i>NOTCH3</i> Genotype and CADASIL Disease SeverityYu-Wen Cheng, Chih-Hao Chen, Chi-Chao Chao, et al.
Neurology. Genetics|May 12, 2021
Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of <i>ATP1A3</i> in Patients Across 3 Global PopulationsKyoko Hoshino, Kathleen J Sweadner, Toshitaka Kawarai, et al.
Pageof 102