Last Updated: 09/26/2026
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Found 6 publications
A novel case of compound heterozygous GFPT1 congenital myasthenic syndrome with a coexisting heterozygous DYSF mutation: clinical and pathological insights.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: September 09, 2025
Reducing body myopathy associated with the LIM2 p.(His123Arg) FHL1 variant.
Journal: Clinical neurology and neurosurgery
Published: February 03, 2021
Polyneuropathy Reveals Origins of Decade-long Gastrointestinal Symptoms in a Patient With Undiagnosed Mitochondrial Neurogastrointestinal Encephalopathy Caused by a Novel Mutation.
Journal: Journal of clinical neuromuscular disease
Published: November 20, 2020
In-hospital mortality and coronary procedure use for individuals with dementia with acute myocardial infarction in the United States.
Journal: Journal of the American Geriatrics Society
Published: November 14, 2013
Showing 1-6 of 6
Last Updated: 09/26/2026