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Di Michele M, Goubau C, Waelkens E, Thys C, De Vos R, Overbergh L, Schyns T, Buyse G, Casaer P, Van Geet C, Freson K. “Functional Studies and Proteomics in Platelets and Fibroblasts Reveal a Lysosomal Defect with Increased Cathepsin-dependent Apoptosis in ATP1A3 Defective Alternating Hemiplegia of Childhood.” Journal of Proteomics (May 13, 2013).

Li SP, Zhang YH, Yang XL, Chen JY, Zeng Q, Zhang J, Wu XR. “Genotype-phenotype Correlation in Patients with Alternating Hemiplegia of Childhood.” Zhonghua Er Ke Za Zhi (Chinese). 2018 Nov 2; 56(11): 811-817. Abstract: https://www.ncbi.nlm.nih.gov/pubmed/30392204

De Vries B, Haan J, Stam AH, Vanmolkot KR, Stoink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD. “Alternating Hemiplegia of Childhood: No Mutations in the Glutamate Transporter EAAT1.” Neuropediatrics (October 2006): 302-304.
Doganli C, et al. “a3Na+/K+-ATPase Deficiency Causes Brain Ventricle Dilation and Abrupt Embryonic Motility in Zebrafish.” J Biol Chem. 288 no. 13 (March 29, 2013): 8862-74.

Duan BC, Wong LC, Lee WT. “Alternating Hemiplegia and Paroxysmal Torticollis Caused by SCN4A Mutation: A New Phenotype?” Neurology. 2019 Oct 8;93(15):673-674. No abstract.

Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Johannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B, ATP1A3 Working Group. “Distinct Neurological Disorders with ATP1A3 Mutations.” Lancet Neurol. 13, no. 5 (May 2014): 503-14.

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.