Last Updated: 11/08/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 6 publications
Juvenile Huntington Disease With Cerebellar-Predominant Atrophy Identified by Genome Sequencing.
Journal: Annals of clinical and translational neurology
Published: July 30, 2026
De novo VPS16 missense variant causes infantile-onset dystonia with defective autophagic flux.
Journal: JCI insight
Published: June 30, 2026
Expanding the Motor Phenotype and Molecular Spectrum of NAA15-Related Disorder: Two Cases of Isolated Childhood-Onset Gait Dystonia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 12, 2026
Movement Disorders in Aicardi-Goutières Syndrome and Response to Immunomodulation.
Journal: Annals of clinical and translational neurology
Published: February 08, 2026
KIF1A-Associated Neurological Disorder (KAND): Spectrum of Movement and Motor Disorders in a Cohort of 51 Patients.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 23, 2026
Childhood-Onset Cerebellar Ataxia from Homozygous XRCC1 c.1293G>C Variant.
Journal: Movement disorders clinical practice
Published: October 14, 2025
Showing 1-6 of 6
Last Updated: 11/08/2026