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Neurology. Genetics|December 21, 2018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer diseaseGary W Beecham, Badri Vardarajan, Elizabeth Blue, et al.
Neurology. Genetics|December 21, 2018
Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in MTFMTDimitri M Hemelsoet, Arnaud V Vanlander, Joél Smet, et al.
Neurology. Genetics|December 26, 2018
Amyloid- and tau-PET imaging in a familial prion kindredDavid T Jones, Ryan A Townley, Jonathan Graff-Radford, et al.
Neurology. Genetics|December 26, 2018
Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylationNam Suk Sim, Youngsuk Seo, Jae Seok Lim, et al.
Neurology. Genetics|February 24, 2018
Familial monophasic acute transverse myelitis due to the pathogenic variant in VPS37AMaureen A Mealy, Tai-Seung Nam, Santiago J Pardo, et al.
Neurology. Genetics|June 24, 2022
Familial Brain Calcifications With Leukoencephalopathy: A Novel PDGFB VariantJack Shen, Amelle Shillington, Alberto J Espay, et al.
Neurology. Genetics|November 19, 2020
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PDLetizia Straniero, Rosanna Asselta, Salvatore Bonvegna, et al.
Neurology. Genetics|May 31, 2021
Diagnosing Mitochondrial Disorders Remains Challenging in the Omics EraPatrick Forny, Emma Footitt, James E Davison, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Neurology. Genetics|February 12, 2020
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Chantall A D Curial, et al.
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