Last Updated: 09/26/2026
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Found 6 publications
Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome.
Journal: Human molecular genetics
Published: November 15, 2022
MRM2 variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneity.
Journal: Journal of medical genetics
Published: February 22, 2022
Measuring ambulation with wrist-based and hip-based activity trackers for children with cerebral palsy.
Journal: Developmental medicine and child neurology
Published: January 21, 2019
The Limb-Girdle Muscular Dystrophies: Is Treatment on the Horizon?
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: July 19, 2018
Kufor-Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese-American Brothers.
Journal: Movement disorders clinical practice
Published: April 27, 2017
The use of tiagabine in pediatric spasticity management.
Journal: Developmental medicine and child neurology
Published: September 07, 2005
Showing 1-6 of 6
Last Updated: 09/26/2026