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.
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.
Incorpora G, Pavone P, Ruggieri M, Cocuzza M, Mazzone L, Parano E, Privitera M. “Neonatal Onset of Hot Water Reflex Seizures in Monozygotic Twins Subsequently Manifesting Episodes of Alternating Hemiplegia.” Epilepsy Research 78, no. 2-3 (February 2008): 225-231.
Bird TD. “Hereditary Ataxia Overview.” GeneReviews. 2019 Apr 18. Fulltext: https://www.ncbi.nlm.nih.gov/books/NBK1138/
Incecik F, Herguner OM. “Alternating Hemiplegia of Childhood in a Child Misdiagnosed as Intractable Epilepsy.” Journal of Neurosciences in Rural Practice Suppl 1 (December 2016): S130-S131.
Boileau S, Vuillaume I, Sablonniere B, Marignier S, Des Portes V, Vallee L, Auvin S. “Absence of T378N Mutation of ATP1A2 Gene in Five Patients with Alternating Hemiplegia of Childhood.” Developmental Medicine and Child Neurology 50, no.11 (November 2008) 879-880.
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.
Sweney MT, Silver K, Gerard-Blanluet M, Pedespan JM, Renault F, Arzimanoglou A, Schlesinger-Massart M, Lewelt AJ, Reyna SP, Swoboda KJ. “Alternating Hemiplegia of Childhood: Early Characteristics and Evolution of a Neurodevelopmental Syndrome.” Pediatrics 123, no. 3 (March 2009): e534-541.
Tochigi M, Iwamoto K, Bundo M, Sasaki T, Kato N, Kato T. “Gene Expression Profiling of Major Depression and Suicide in the Prefrontal Cortex of Postmortem Brains.” Neuroscience Research (February 2008): 184-191.
Nakashima T, Yasuda K, Kobayashi M, Wada H, Ishii A, Hirose S. “Heart Rate Variability in a Patient with Alternating Hemiplegia.” Intractable Rare Diseases Research. 2019 May; 8(2): 134-137. Fulltext: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557234/
Andermann F, Ohtahara S, Andermann E, Camfield P, Kobayashi K. “Infantile Hypotonia and Paroxysmal Dystonia: A Variant of Alternating Hemiplegia of Childhood.” Movement Disorders.9, no.2 (March 1994): 227-229.