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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.

Ishihara N, Inagaki H, Miyake M, Kawamura Y, Yoshikawa t, Kurahashi H. “A Case of Early Onset Life-threatening Epilepsy Associated with a Novel ATP1A3 Gene Variant.” Brain & Development. 2019 Mar; 41(3): 285-291. Abstract: https://www.brainanddevelopment.com/article/S0387-7604(18)30256-0/fulltext

Marzin P, Mignot C, Dorison N, Dufour L, Ville D, Kaminska A, Panagiotakaki E, Dienpendaele AS, Penniello MJ, Nougues MC, Keren B, Depienne C, Nava C, Milh M, Villard L, Richelme C, Rivier C, Whalen S, Heron D, Lesca G, Doummar D. “Early-onset Encephalopathy with Paroxysmal Movement Disorders and Epileptic Seizures without Hemiplegic Attacks: About Three Children with Novel ATP1A3 Mutations.” Brain Development. 2018 Oct; 40(9): 768-774. Abstract: https://www.sciencedirect.com/science/article/pii/S0387760418302146?via%3Dihub

Neupert D, Abbassi P, Prange L, Flamini R, Mikati MA. Progression of alternating hemiplegia of childhood-related focal epilepsy to electrical status epilepticus in sleep with reversible encephalopathy. Epileptic Disord. 2022 Feb 1;24(1):183-190. Abstract: https://pubmed.ncbi.nlm.nih.gov/34789444/

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).