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Spina S, Antoniuk S, Bruk I, Crippa A. “Post-ictal EEG Findings in a Patient Diagnosed with Alternating Hemiplegia of Childhood (AHC).” Journal of the Neurological Sciences 333, Supplement 1 (October 2013): e630.

Sharawat IK, Saini L. “Recurrent Focal Seizures and Transient Hemiparesis: Think About Alternating Hemiplegia of Childhood.” Pediatric Neurology. 2018 Mar; 80: 97-98. Abstract: https://www.pedneur.com/article/S0887-8994(17)31152-9/abstract

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.

Holze N, Baalen AV, Stephani U, Helbig I, Muhle H. “Variants in the ATP1A3 Gene Mutations within Severe Apnea Starting in Early Infancy: An Observational Study of Two Cases with a Possible Relation to Epileptic Activity.” Neuropediatrics. 2018 Oct; 49(5): 342-346. Abstract: https://www.thieme-connect.com/DOI/DOI?10.1055/s-0038-1653978

Bassi MT, Bresolin N, Tonelli A. “A Novel Mutation in the ATP1A2 Gene Causes Alternating Hemiplegia of Childhood.” Journal of Medical Genetics 41 (2004,): 621-628.