Back Donate
Donate
Default image for pages

Uchitel J, Helseth A, Prange L, McLean M, Ghusayni R, Sachdev M, Hunanyan A, Mikati MA. “The Epileptology of Alternating Hemiplegia of Childhood.” Neurology. 2019 Sep 24;93(13): e1248-e1259. Abstract: https://www.ncbi.nlm.nih.gov/pubmed/31484714

Al-Bulushi B, Al-Hashem A, Tabarki B. “A Wide Clinical Phenotype Spectrum in Patients with ATP1A2 Mutations.” J Child Neurol. (February 2014).

Alexoudi, A, Schneider, SA. “Alternating Hemiplegia of Childhood and Rapid-onset Dystonia Parkinsonism are Allelic Disorders Due to ATP1A3 Gene Mutations.” Movement Disorders (October 2012): 1494-.

Aminkeng, F. “Mutations in ATP1A3 Cause Alternating Hemiplegia of Childhood.” Clinical Genetics 83, no.1 (January 2013): 32-33.

Gasser M, Boonsimma P, Netbaramee W, Wechapinan T, Srichomthomg C, Ittiwut C, Krenn M, Zimprich F, et al. “ATP1A3-related Epilepsy: Report of Seven Cases and Literature-based Analysis of Treatment Response.” J Clin Neurosci. 2020 Jan 17. Abstract: https://www.ncbi.nlm.nih.gov/pubmed/31959558

Azarias, et al. “A Specific and Essential Role for NA.K-ATPase a 3 in Neurons Co-expressing a 1 a 3.” J Biol Chem. 288, no. 4 (January 25, 2013): 2734-43.

Shafer ME, Mayfield JW, McDonald F. “Alternating Hemiplegia of Childhood: A Study of Neuropsychological Functioning.” Applied Neuropsychology 12, no. 1 (2005): 49-56.

Smedemark-Margulies N, Brownstein CA, Vargas S, Tembulkar SK, Towne, MC, Shi J, et. al. “A Novel de Novo Mutation in ATP1A3 and Childhood-onset Schizophrenia.” Cold Spring Harb Mol Case Studies 2, no. 5 (Setptember 2016): 1008-.

Sugimoto H, Ikeda K, Kawakami K. “Atp1a3-deficient Heterozygous Mice Show Lower Rank in the Hierarchy and Altered Social Behavior.” Genes Brain Behav. 2017 Oct 23.

Sweney M, Newcomb T, Swoboda K. “The Expanding Spectrum of Neurological Phenotypes in Children with ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond.” Pediatric Neurolog (January 2015): 56-64.