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Neurology|February 26, 2016
A randomized trial of mexiletine in ALS: Safety and effects on muscle cramps and progressionMichael D Weiss, Eric A Macklin, Zachary Simmons, et al.Neurology. Genetics|October 27, 2022
Investigating Late-Onset Pompe Prevalence in Neuromuscular Medicine Academic Practices: The IPaNeMA StudyMarie Wencel, Aziz Shaibani, Namita A Goyal, et al.Plos One|April 25, 2013
Design and initial results of a multi-phase randomized trial of ceftriaxone in amyotrophic lateral sclerosisJames D Berry, Jeremy M Shefner, Robin Conwit, et al.Annals of Neurology|February 27, 2013
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophyKevin M Flanigan, Ermelinda Ceco, Kay-Marie Lamar, et al.The Lancet. Neurology|April 2, 2013
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man studyTimothy M Miller, Alan Pestronk, William David, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 15, 2019
Selection design phase II trial of high dosages of tamoxifen and creatine in amyotrophic lateral sclerosisSuma Babu, Eric A Macklin, Katherine E Jackson, et al.Neurology|February 12, 2016
Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysisValeria A Sansone, James Burge, Michael P McDermott, et al.Biorxiv : the Preprint Server for Biology|February 20, 2025
Identifying and treating CLN3 disease outside the central nervous systemEwa A Ziółkowska, Albina Jablonka-Shariff, Letitia L Williams, et al.Annals of Neurology|January 23, 2015
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45Andrew R Findlay, Nicolas Wein, Yuuki Kaminoh, et al.Journal of Cachexia, Sarcopenia and Muscle|August 15, 2025
High-Density Lipoprotein-Associated Cholesterol Abnormalities in a Clinical Outcomes Study of Dysferlin-Deficient Limb-Girdle Muscular Dystrophy Type R2Zoe White, Laura Rufibach, Heather Gordish Dressman, et al.Pageof 14