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

Neurogenetics

Showing results (681-690 of 949) with videos related to

Pageof 95
Sort By:
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
Neurogenetics|March 29, 2021
Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasiaAli S Shalash, Thomas W Rösler, Mohamed Salama, et al.
Neurogenetics|August 9, 2025
Computational association in parkinson's disease SNPs with brain structural and functional alterationsSwetha Subramaniyan, Beena Briget Kuriakose, Vijay Nattan, et al.
Neurogenetics|July 19, 2025
Moyamoya disease presenting with transient nonfocal neurological attacks in an Indian woman carrying a previously unreported RNF213 missense variant (p.Thr554Ile)Ritwick Mondal, Shramana Deb, Nirmalya Ray, et al.
Neurogenetics|June 18, 2025
Strabismus and nystagmus in oculocutaneous albinism: clinical perspectives, diagnosis, and role of neurotransmittersVaishali Dobhal, Ashwani Kumar, Ishu Garg, et al.
Neurogenetics|May 26, 2025
A heterozygous variation of PINK1 is potentially associated with essential tremor in a Chinese familyBin Wang, Bin Wei, Likui Lu, et al.
Neurogenetics|July 18, 2024
Kufor-Rakeb syndrome-associated psychosis: a novel loss-of-function ATP13A2 variant and response to antipsychotic therapyMark Ainsley Colijn, Stephanie Vrijsen, Ping Yee Billie Au, et al.
Neurogenetics|July 8, 2024
TREK-1 channel as a therapeutic target for dexmedetomidine-mediated neuroprotection in cerebral ischemiaYang Xu, XiaoDan Teng, Ming Wei, et al.
Neurogenetics|July 8, 2024
Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient originTiyasha De, Pooja Sharma, Bharathram Upilli, et al.
Neurogenetics|February 9, 2024
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literatureEttore Cioffi, Gianluca Coppola, Olimpia Musumeci, et al.
Pageof 95

Showing results (681-690 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
Neurogenetics|March 29, 2021
Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasiaAli S Shalash, Thomas W Rösler, Mohamed Salama, et al.
Neurogenetics|August 9, 2025
Computational association in parkinson's disease SNPs with brain structural and functional alterationsSwetha Subramaniyan, Beena Briget Kuriakose, Vijay Nattan, et al.
Neurogenetics|July 19, 2025
Moyamoya disease presenting with transient nonfocal neurological attacks in an Indian woman carrying a previously unreported RNF213 missense variant (p.Thr554Ile)Ritwick Mondal, Shramana Deb, Nirmalya Ray, et al.
Neurogenetics|June 18, 2025
Strabismus and nystagmus in oculocutaneous albinism: clinical perspectives, diagnosis, and role of neurotransmittersVaishali Dobhal, Ashwani Kumar, Ishu Garg, et al.
Neurogenetics|May 26, 2025
A heterozygous variation of PINK1 is potentially associated with essential tremor in a Chinese familyBin Wang, Bin Wei, Likui Lu, et al.
Neurogenetics|July 18, 2024
Kufor-Rakeb syndrome-associated psychosis: a novel loss-of-function ATP13A2 variant and response to antipsychotic therapyMark Ainsley Colijn, Stephanie Vrijsen, Ping Yee Billie Au, et al.
Neurogenetics|July 8, 2024
TREK-1 channel as a therapeutic target for dexmedetomidine-mediated neuroprotection in cerebral ischemiaYang Xu, XiaoDan Teng, Ming Wei, et al.
Neurogenetics|July 8, 2024
Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient originTiyasha De, Pooja Sharma, Bharathram Upilli, et al.
Neurogenetics|February 9, 2024
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literatureEttore Cioffi, Gianluca Coppola, Olimpia Musumeci, et al.
Pageof 95