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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.

De Koning, Tom J, Marina Tijssen. “Movement Disorders in 2014: Genetic Advances Spark a Revolution in Dystonia Phenotyping.” Nature Reviews Neurology (January 2015).

Van Egmond, Kuiper A, Eggink H, Sinke R, Brouwer O, Verschuuren-Bemelmans C, Divak D, Tijssen M, de Koning T. “Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm.” Journal of Neurology, Neurosurgery and Psychiatry (November 13, 2014).

Aicardi J. “Alternating Hemiplegia of Childhood.” in Epilepsy and Movement Disorders, ed. G Renzo et al. (Cambridge University Press, 2002), 379-392.

Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. “ATP1A3 Mosaicism in Families with Alternating Hemiplegia of Childhood.” Clin Genet. 2019 Jul; 96(1): 43-52. Abstract: https://www.ncbi.nlm.nih.gov/pubmed/30891744

Yang X, Gao H, Zhang J, Xu X, Liu X, Wu X, Wei L, Zhang Y. “ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients.” PLos ONE 9, no. 5 (May 2014).

Yang X, Zhang Y, Yuan D, Xu X, Li S, Wei L, Wu Y, Xiong H, Liu X, Bao X, Jiang Y, Wu X. “ATP1A3 Gene Mutations in Patients with Alternating Hemiplegia of Childhood.” Zhongua Er Ke Za Zhi (November 2015). (Chinese)

Yano S, Silver K, Young R, DeBrosse S, Ebel R, Swoboda K, Acsadi G. “Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation.” Pediatric Neurology 73 (August 2017): 101-105.