Last Updated: 09/26/2026
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Found 11 publications
Lisdexamfetamine Therapy in Paroxysmal Non-kinesigenic Dyskinesia Associated with the KCNMA1-N999S Variant.
Journal: Movement disorders clinical practice
Published: August 13, 2021
An emerging spectrum of variants and clinical features in KCNMA1-linked channelopathy.
Journal: Channels (Austin, Tex.)
Published: July 05, 2021
PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.
Journal: Neurology. Genetics
Published: November 03, 2020
Cataplexy in Patients Harboring the KCNMA1 p.N999S Mutation.
Journal: Movement disorders clinical practice
Published: March 11, 2020
Automated spectrographic seizure detection using convolutional neural networks.
Journal: Seizure
Published: May 21, 2019
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature.
Journal: Journal of medical genetics
Published: July 27, 2017
Increasing Ketamine Use for Refractory Status Epilepticus in US Pediatric Hospitals.
Journal: Journal of child neurology
Published: March 29, 2017
Retinoic Acid-Mediated Regulation of GLI3 Enables Efficient Motoneuron Derivation from Human ESCs in the Absence of Extrinsic SHH Activation.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: August 21, 2015
Reduction in focal ictal activity following transplantation of MGE interneurons requires expression of the GABAA receptor α4 subunit.
Journal: Frontiers in cellular neuroscience
Published: January 16, 2015
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Last Updated: 09/26/2026