Last Updated: 09/26/2026
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Found 7 publications
A Diagnostic Conundrum: Atypical McArdle Disease Mimic With Heterozygous PYGM Mutation and Cytochrome C Oxidase (COX)-Negative Fibers.
Journal: Cureus
Published: May 27, 2026
COVID-19 and MOG-IgG-associated acquired demyelinating polyneuropathy compatible with chronic inflammatory demyelinating polyneuropathy in a previously healthy girl.
Journal: Proceedings (Baylor University. Medical Center)
Published: August 22, 2022
Postinfectious SARS-CoV-2 Opsoclonus-Myoclonus-Ataxia Syndrome.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: January 02, 2022
Subjective-objective sleepiness discrepancy in adult-onset myotonic dystrophy type 1.
Journal: Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine
Published: October 20, 2021
Teaching NeuroImages: Colchicine-induced vacuolar myopathy.
Journal: Neurology
Published: December 11, 2019
Visual, Ocular Motor, and Cochleo-Vestibular Loss in Patients With Heteroplasmic, Maternally-Inherited Diabetes Mellitus and Deafness (MIDD), 3243 Transfer RNA Mutation.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: January 08, 2016
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Last Updated: 09/26/2026