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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 6, 2010
A pilot study of the prevalence of psychiatric disorders in PLS and ALSEdward D Huey, Jeremy Koppel, Nicole Armstrong, et al.Neuroimage|September 12, 2009
Reliability of fiber tracking measurements in diffusion tensor imaging for longitudinal studyLaura E Danielian, Nobue K Iwata, David M Thomasson, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 30, 2010
Towards a user-friendly brain-computer interface: initial tests in ALS and PLS patientsOu Bai, Peter Lin, Dandan Huang, et al.Neurobiology of Aging|January 9, 2021
Longitudinal changes in network homogeneity in presymptomatic C9orf72 mutation carriersRebecca E Waugh, Laura E Danielian, Rachel F Smallwood Shoukry, et al.Neuroimage. Clinical|November 2, 2013
Structural imaging differences and longitudinal changes in primary lateral sclerosis and amyotrophic lateral sclerosisJustin Y Kwan, Avner Meoded, Laura E Danielian, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Clinical care and therapeutic trials in PLSMary Kay Floeter, Deborah Warden, Dale Lange, et al.Journal of Neural Engineering|March 4, 2008
A high performance sensorimotor beta rhythm-based brain-computer interface associated with human natural motor behaviorOu Bai, Peter Lin, Sherry Vorbach, et al.Neurologic Clinics|October 31, 2015
Primary Lateral SclerosisJeffrey M Statland, Richard J Barohn, Mazen M Dimachkie, et al.Muscle & Nerve|October 28, 2006
Terminal latency index in neuropathy with antibodies against myelin-associated glycoproteinsVitalie D Lupu, Carlos A Mora, Jim Dambrosia, et al.Muscle & Nerve|January 23, 2016
Cortical hyperexcitability in patients with C9ORF72 mutations: Relationship to phenotypeOlivia Schanz, Devin Bageac, Laura Braun, et al.Pageof 8