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Muscle & Nerve|February 12, 2025
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral SclerosisAlexander H Morrison, Jose Victor Jimenez, Jesse Y Hsu, et al.
The European Respiratory Journal|February 8, 2019
Development of a prognostic model of respiratory insufficiency or death in amyotrophic lateral sclerosisJason Ackrivo, John Hansen-Flaschen, E Paul Wileyto, et al.
Plos One|August 22, 2014
Linear associations between clinically assessed upper motor neuron disease and diffusion tensor imaging metrics in amyotrophic lateral sclerosisJohn H Woo, Sumei Wang, Elias R Melhem, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 9, 2014
Deficits in sentence expression in amyotrophic lateral sclerosisSharon Ash, Christopher Olm, Corey T McMillan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Cognitive reserve in ALS: The role of occupational skills and requirementsEmma Rhodes, Sebleh Alfa, Hannah Jin, et al.
Neurology|July 18, 2020
Automated analysis of natural speech in amyotrophic lateral sclerosis spectrum disordersNaomi Nevler, Sharon Ash, Corey McMillan, et al.
American Journal of Respiratory and Critical Care Medicine|July 20, 2019
Classifying Patients with Amyotrophic Lateral Sclerosis by Changes in FVC. A Group-based Trajectory AnalysisJason Ackrivo, John Hansen-Flaschen, Bobby L Jones, et al.
Neurology|July 4, 2014
Narrative discourse deficits in amyotrophic lateral sclerosisSharon Ash, Anna Menaged, Christopher Olm, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 9, 2024
Cognitive reserve in ALS: the role of occupational skills and requirementsEmma Rhodes, Sebleh Alfa, Hannah A Jin, et al.
Plos One|June 22, 2012
Microglial activation correlates with disease progression and upper motor neuron clinical symptoms in amyotrophic lateral sclerosisJohannes Brettschneider, Jon B Toledo, Vivianna M Van Deerlin, et al.
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