Showing results (71-80 of 849) with videos related to
Sort By:
Pageof 85
Neurology. Genetics|June 9, 2018
Erratum: Expanding the global prevalence of spinocerebellar ataxia type 42Neurology. Genetics|May 31, 2018
ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementiaKang Zhang, Qing Liu, Keqiang Liu, et al.Neurology. Genetics|May 31, 2018
Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016Marie Ryan, Mark Heverin, Mark A Doherty, et al.Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in VPS13A detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.Neurology. Genetics|November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletionsDiana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.Neurology. Genetics|November 9, 2016
SORL1 mutations in early- and late-onset Alzheimer diseaseMichael L Cuccaro, Regina M Carney, Yalun Zhang, et al.Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.Neurology. Genetics|November 2, 2020
Integrative analysis identifies the association between CASZ1 methylation and ischemic strokeXing-Bo Mo, Huan Zhang, Ai-Li Wang, et al.Neurology. Genetics|November 2, 2020
Identification of a novel mutation in ATP13A2 associated with a complicated form of hereditary spastic paraplegiaYasuko Odake, Kishin Koh, Yoshihisa Takiyama, et al.Neurology. Genetics|November 2, 2020
Congenital immobility and stiffness related to biallelic ATAD1 variantsRoxane Bunod, Diane Doummar, Sandra Whalen, et al.Pageof 85