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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 6, 2025
Respiratory function, survival, and NIV prevalence over time in ALS - a PRECISION ALS studyStefan Sennfält, Ammar Al-Chalabi, Alejandro Caravaca Puchades, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 6, 2025
Real-world prognostic role of riluzole use in ALS: a multi-center study from PRECISION-ALSRosario Vasta, Fouke Ombelet, Frederik Hobin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 6, 2025
Clinical trajectories of genetic variants in ALS: a European observational study within PRECISION-ALSRobert McFarlane, Sarah Opie-Martin, Alejandro Caravaca Puchades, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 6, 2025
Mapping the natural history of amyotrophic lateral sclerosis: time-to-event analysis of clinical milestones in the pan-European, population-based PRECISION-ALS cohortAlejandro Caravaca Puchades, Harry E McDonough, Ammar Al-Chalabi, et al.
Plos Medicine|January 30, 2018
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Plos Medicine|January 10, 2018
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.
Genome Medicine|January 19, 2022
Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1Restuadi Restuadi, Frederik J Steyn, Edor Kabashi, et al.
Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
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