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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 24, 2024
A comparison between bioelectrical impedance analysis and air-displacement plethysmography in assessing fat-free mass in patients with motor neurone diseases: a cross-sectional studyMark R Janse van Mantgem, Maaike L Soors D'Ancona, Myrte Meyjes, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 3, 2024
Quantitative susceptibility mapping in amyotrophic lateral sclerosis: automatic quantification of the magnetic susceptibility in the subcortical nucleiSadegh Ghaderi, Farzad Fatehi, Sanjay Kalra, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 7, 2024
REVEALS-a longitudinal cohort study of multifaceted respiratory assessment in ALSJames Rooney, Deirdre Murray, Dara Meldrum, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 8, 2024
Treatment continuity of amyotrophic lateral sclerosis with available riluzole formulations: state of the art and current challenges in a 'real-world' settingPhilippe Corcia, Nathalie Guy, Pierre-François Pradat, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 21, 2023
Prevalence of amyotrophic lateral sclerosis in the United States, 2018Paul Mehta, Jaime Raymond, Yuzi Zhang, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 22, 2023
LAENALS: epidemiological and clinical features of amyotrophic lateral sclerosis in Latin AmericaBeatriz Vélez-GóMEZ, Abayuba Perna, Cristina Vazquez, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 18, 2023
Genetic overlap between ALS and other neurodegenerative or neuromuscular disordersCathrine Goberg Olsen, Øyvind Løvold Busk, Øystein Lunde Holla, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 5, 2023
Describing and characterising variability in ALS disease progressionMuzammil Arif Din Abdul Jabbar, Ling Guo, Yang Guo, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 13, 2023
A speech-based prognostic model for dysarthria progression in ALSGabriela Stegmann, Sherman Charles, Julie Liss, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 5, 2018
Moral judgment in patients with behavioral variant of frontotemporal dementia and amyotrophic lateral sclerosis: no impairment of the moral position, but rather its executionElisa Semler, Lukas Petersdorff, Sarah Anderl-Straub, et al.
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