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Muscle & Nerve|June 16, 2011
An interactive voice response diary for patients with non-dystrophic myotoniaJeffrey M Statland, Yunxia Wang, Rachel Richesson, et al.Frontiers in Artificial Intelligence|July 25, 2022
Pilot Study of Real-World Monitoring of the Heart Rate Variability in Amyotrophic Lateral SclerosisAlexander A Brown, Bradley J Ferguson, Vovanti Jones, et al.Scientific Reports|May 27, 2021
Oxaloacetate treatment preserves motor function in SOD1G93A mice and normalizes select neuroinflammation-related parameters in the spinal cordSudheer K Tungtur, Heather M Wilkins, Robert S Rogers, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 9, 2008
Creatine monohydrate in ALS: effects on strength, fatigue, respiratory status and ALSFRSJeffrey Rosenfeld, Ruth M King, Carlayne E Jackson, et al.Neurology|October 15, 2014
Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies [RETIRED]: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic MedicinePushpa Narayanaswami, Michael Weiss, Duygu Selcen, et al.Archives of Neurology|March 12, 2008
Amyotrophic lateral sclerosis with ragged-red fibersMichio Hirano, Corrado Angelini, Pasquale Montagna, et al.Movement Disorders Clinical Practice|August 18, 2021
Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT VariantsLaura Williams, Diana A Olszewska, Conor Fearon, et al.Journal of Clinical Neuromuscular Disease|August 23, 2017
Less is More in Diabetic Neuropathy Diagnosis: Comparison of Quantitative Sudomotor Axon Reflex and Skin BiopsyAhmad R Abuzinadah, Patricia Kluding, Douglas Wright, et al.Archives of Neurology|August 10, 2005
Supportive care for patients with Guillain-Barré syndromeRichard A C Hughes, Eelco F M Wijdicks, Estelle Benson, et al.Journal of Clinical Neuromuscular Disease|December 17, 2008
Primary lateral sclerosis: clinical and laboratory features in 25 patientsMike A Singer, Suleiman Kojan, Richard J Barohn, et al.Pageof 19