Last Updated: 09/26/2026
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Found 9 publications
Benign nocturnal alternating hemiplegia of childhood: A clinical and nomenclatural reappraisal.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: June 06, 2018
Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation.
Journal: Pediatric neurology
Published: February 07, 2017
Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders.
Journal: Neurology. Genetics
Published: August 25, 2016
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
Journal: PloS one
Published: September 01, 2015
A 13-year old female with intractable seizures.
Journal: Brain pathology (Zurich, Switzerland)
Published: February 14, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
Journal: PloS one
Published: December 12, 2014
Narcolepsy with cataplexy as presenting symptom of occult neuroblastoma.
Journal: Pediatric neurology
Published: September 28, 2012
A multidisciplinary approach to the treatment of anti-NMDA-receptor antibody encephalitis: a case and review of the literature.
Journal: The Journal of neuropsychiatry and clinical neurosciences
Published: July 10, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Journal: Nature genetics
Published: April 16, 2012
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Last Updated: 09/26/2026