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Brain : a Journal of Neurology|September 26, 2022
The impact of age on genetic testing decisions in amyotrophic lateral sclerosisPuja R Mehta, Alfredo Iacoangeli, Sarah Opie-Martin, et al.
Brain : a Journal of Neurology|February 8, 2018
HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth diseaseVeronick Benoy, Lawrence Van Helleputte, Robert Prior, et al.
Neurology|May 3, 2015
Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosisChing-Hua Lu, Corrie Macdonald-Wallis, Elizabeth Gray, et al.
Nature Reviews. Neurology|December 19, 2020
Improving clinical trial outcomes in amyotrophic lateral sclerosisMatthew C Kiernan, Steve Vucic, Kevin Talbot, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 30, 2020
Measuring quality of life in ALS/MND: validation of the WHOQOL-BREFCarolyn A Young, Roger Mills, Ammar Al-Chalabi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 15, 2018
Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brainsMichael J Keogh, Wei Wei, Juvid Aryaman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Frequency and signature of somatic variants in 1461 human brain exomesWei Wei, Michael J Keogh, Juvid Aryaman, et al.
Brain Pathology (Zurich, Switzerland)|July 24, 2022
Atypical TDP-43 protein expression in an ALS pedigree carrying a p.Y374X truncation mutation in TARDBPJohnathan Cooper-Knock, Thomas H Julian, Emily Feneberg, et al.
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