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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 11, 2024
Dyspnea (breathlessness) in amyotrophic lateral sclerosis/motor neuron disease: prevalence, progression, severity, and correlatesCarolyn A Young, Amina Chaouch, Christopher J Mcdermott, et al.
Brain : a Journal of Neurology|January 25, 2012
A proposed staging system for amyotrophic lateral sclerosisJose C Roche, Ricardo Rojas-Garcia, Kirsten M Scott, et al.
Brain Communications|January 16, 2025
Lipid-mediated resolution of inflammation and survival in amyotrophic lateral sclerosisOzlem Yildiz, Guy P Hunt, Johannes Schroth, et al.
Neuroimage|August 4, 2020
Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T applied to amyotrophic lateral sclerosisChaoyue Wang, Sean Foxley, Olaf Ansorge, et al.
Nature Communications|November 26, 2021
Axonal TDP-43 condensates drive neuromuscular junction disruption through inhibition of local synthesis of nuclear encoded mitochondrial proteinsTopaz Altman, Ariel Ionescu, Amjad Ibraheem, et al.
Human Mutation|October 20, 2011
A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N)Heather M McLaughlin, Reiko Sakaguchi, William Giblin, et al.
Scientific Reports|January 25, 2017
Whole-exome sequencing of 228 patients with sporadic Parkinson's diseaseCynthia Sandor, Frantisek Honti, Wilfried Haerty, et al.
Human Mutation|August 30, 2012
A loss-of-function variant in the human histidyl-tRNA synthetase (HARS) gene is neurotoxic in vivoAimée Vester, Gisselle Velez-Ruiz, Heather M McLaughlin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 8, 2020
Primary lateral sclerosis: consensus diagnostic criteriaMartin R Turner, Richard J Barohn, Philippe Corcia, et al.
Archives of Neurology|January 14, 2009
Diffusion tensor imaging in sporadic and familial (D90A SOD1) forms of amyotrophic lateral sclerosisBiba R Stanton, Daisy Shinhmar, Martin R Turner, et al.
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