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Eclinicalmedicine|December 19, 2022
Patient reported impact of symptoms in amyotrophic lateral sclerosis (PRISM-ALS): A national, cross-sectional studyChristine Zizzi, Jamison Seabury, Spencer Rosero, et al.Frontiers in Neurology|September 15, 2023
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegiaAmokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 16, 2023
The amyotrophic lateral sclerosis-health index (ALS-HI): development and evaluation of a novel outcome measureAnika Varma, Jennifer Weinstein, Jamison Seabury, et al.Annals of Clinical and Translational Neurology|April 25, 2015
Identification of distinct circulating exosomes in Parkinson's diseasePaul R Tomlinson, Ying Zheng, Roman Fischer, et al.Muscle & Nerve|January 31, 2022
Phase 2B randomized controlled trial of NP001 in amyotrophic lateral sclerosis: Pre-specified and post hoc analysesRobert G Miller, Rongzhen Zhang, Paige M Bracci, 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.Neuroepidemiology|November 29, 2008
Geographical clustering of amyotrophic lateral sclerosis in South-East England: a population studyKirsten M Scott, Kumar Abhinav, Biba R Stanton, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2014
Health utility decreases with increasing clinical stage in amyotrophic lateral sclerosisAshley R Jones, Naheed Jivraj, Rubika Balendra, et al.Nature Medicine|July 27, 2026
Longitudinal plasma proteomics predict phenoconversion to clinically manifest ALSXiming Ran, Joanne Wuu, Zhaohui S Qin, et al.Pageof 42