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 (431-440 of 842) with videos related to

Pageof 85
Sort By:
Neurology. Genetics|July 12, 2021
Effect of Body Weight on Age at Onset in Huntington Disease: A Mendelian Randomization StudyJorien M M van der Burg, Patrick Weydt, Georg Bernhard Landwehrmeyer, et al.
Neurology. Genetics|May 6, 2022
Biallelic <i>ATOH1</i> Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing LossTanja Višnjar, Aleš Maver, Karin Writzl, et al.
Neurology. Genetics|June 3, 2022
Vanishing White Matter Disease Presenting as Dementia and Infertility: A Case ReportJasmine Parihar, Deepti Vibha, Roopa Rajan, et al.
Neurology. Genetics|June 17, 2022
Adult-Onset Sandhoff Disease in a Filipino Patient: Asymmetric Weakness, Whole <i>HEXB</i> Gene Deletion, and Coexisting <i>MYH7</i> Pathogenic VariantGrayson Beecher, Teerin Liewluck, Margherita Milone
Neurology. Genetics|September 22, 2016
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis riskBrooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Neurology. Genetics|June 8, 2017
<i>ARHGEF9</i> disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.
Neurology. Genetics|June 8, 2017
Intramyocellular lipid excess in the mitochondrial disorder MELAS: MRS determination at 7TSailaja Golla, Jimin Ren, Craig R Malloy, et al.
Neurology. Genetics|February 7, 2022
Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular InvolvementIyas Daghlas, Muralidharan Sargurupremraj, Rebecca Danning, et al.
Neurology. Genetics|February 21, 2022
Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical FeaturesYu-Lan Chen, Dian-Fu Chen, Hua-Zhen Ke, et al.
Neurology. Genetics|July 13, 2022
A Biallelic Variant in <i>FRA10AC1</i> Is Associated With Neurodevelopmental Disorder and Growth RetardationNorah Alsaleh, Amal Alhashem, Brahim Tabarki, et al.
Pageof 85

Showing results (431-440 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|July 12, 2021
Effect of Body Weight on Age at Onset in Huntington Disease: A Mendelian Randomization StudyJorien M M van der Burg, Patrick Weydt, Georg Bernhard Landwehrmeyer, et al.
Neurology. Genetics|May 6, 2022
Biallelic <i>ATOH1</i> Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing LossTanja Višnjar, Aleš Maver, Karin Writzl, et al.
Neurology. Genetics|June 3, 2022
Vanishing White Matter Disease Presenting as Dementia and Infertility: A Case ReportJasmine Parihar, Deepti Vibha, Roopa Rajan, et al.
Neurology. Genetics|June 17, 2022
Adult-Onset Sandhoff Disease in a Filipino Patient: Asymmetric Weakness, Whole <i>HEXB</i> Gene Deletion, and Coexisting <i>MYH7</i> Pathogenic VariantGrayson Beecher, Teerin Liewluck, Margherita Milone
Neurology. Genetics|September 22, 2016
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis riskBrooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Neurology. Genetics|June 8, 2017
<i>ARHGEF9</i> disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.
Neurology. Genetics|June 8, 2017
Intramyocellular lipid excess in the mitochondrial disorder MELAS: MRS determination at 7TSailaja Golla, Jimin Ren, Craig R Malloy, et al.
Neurology. Genetics|February 7, 2022
Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular InvolvementIyas Daghlas, Muralidharan Sargurupremraj, Rebecca Danning, et al.
Neurology. Genetics|February 21, 2022
Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical FeaturesYu-Lan Chen, Dian-Fu Chen, Hua-Zhen Ke, et al.
Neurology. Genetics|July 13, 2022
A Biallelic Variant in <i>FRA10AC1</i> Is Associated With Neurodevelopmental Disorder and Growth RetardationNorah Alsaleh, Amal Alhashem, Brahim Tabarki, et al.
Pageof 85