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Neurology. Clinical Practice|April 12, 2021
Facial Onset Sensory and Motor Neuronopathy: New Cases, Cognitive Changes, and PathophysiologyEva M J de Boer, Andrew W Barritt, Marwa Elamin, et al.
Frontiers in Cellular Neuroscience|March 20, 2023
Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survivalBrett N Adey, Johnathan Cooper-Knock, Ahmad Al Khleifat, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Nature Communications|August 29, 2024
ATAXIN-2 intermediate-length polyglutamine expansions elicit ALS-associated metabolic and immune phenotypesRenata Vieira de Sá, Emma Sudria-Lopez, Marta Cañizares Luna, et al.
NPJ Genomic Medicine|March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosisMarta F Nabais, Tian Lin, Beben Benyamin, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Annals of Neurology|June 17, 2014
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisFrank P Diekstra, Vivianna M Van Deerlin, John C van Swieten, et al.
Genome Biology|June 29, 2016
Blood lipids influence DNA methylation in circulating cellsKoen F Dekkers, Maarten van Iterson, Roderick C Slieker, et al.
Human Molecular Genetics|August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosisHylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.
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