Last Updated: 09/26/2026
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Found 28 publications
Electrodiagnostic Studies as a Diagnostic and Prognostic Tool in Acute Flaccid Myelitis.
Journal: Muscle & nerve
Published: August 04, 2025
Treatment Patterns and Disease Burden of Juvenile Myasthenia Gravis in the United States: A Cohort Study Using Health Care Claims Databases.
Journal: Neurology
Published: June 09, 2025
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Journal: American journal of human genetics
Published: December 08, 2023
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
Journal: NPJ genomic medicine
Published: October 23, 2023
Sexual and Gender Diversity in Pediatric Neurology: Why We Care.
Journal: Pediatric neurology
Published: April 04, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
Journal: NPJ genomic medicine
Published: December 15, 2022
Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice.
Journal: International journal of molecular sciences
Published: June 01, 2022
Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force.
Journal: Annals of neurology
Published: July 19, 2021
Pathologic Findings Associated With a Case of Acute Flaccid Myelitis.
Journal: Journal of neuropathology and experimental neurology
Published: April 19, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Journal: American journal of human genetics
Published: January 20, 2021
Last Updated: 09/26/2026