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4. Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation. Ju J; Hirose S; Shi XY; Ishii A; Hu LY; Zou LP Orphanet J Rare Dis; 2016 May; 11(1):55. PubMed ID: 27146299 [TBL] [Abstract][Full Text] [Related]
5. De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. Kanemasa H; Fukai R; Sakai Y; Torio M; Miyake N; Lee S; Ono H; Akamine S; Nishiyama K; Sanefuji M; Ishizaki Y; Torisu H; Saitsu H; Matsumoto N; Hara T BMC Neurol; 2016 Sep; 16():174. PubMed ID: 27634470 [TBL] [Abstract][Full Text] [Related]
6. [Alternating hemiplegia of childhood: ATP1A3 gene analysis in 16 patients]. Ulate-Campos A; Fons C; Campistol J; Martorell L; Cancho-Candela R; Eiris J; López-Laso E; Pineda M; Sans A; Velázquez R Med Clin (Barc); 2014 Jul; 143(1):25-8. PubMed ID: 24768197 [TBL] [Abstract][Full Text] [Related]
7. Alternating hemiplegia of childhood with a de novo mutation in ATP1A3 and changes in SLC2A1 responsive to a ketogenic diet. Ulate-Campos A; Fons C; Artuch R; Castejón E; Martorell L; Ozelius L; Pascual J; Campistol J Pediatr Neurol; 2014 Apr; 50(4):377-9. PubMed ID: 24491413 [TBL] [Abstract][Full Text] [Related]
12. ATP1A3-related phenotypes in Chinese children: AHC, CAPOS, and RECA. Huang D; Song X; Ma J; Li X; Guo Y; Li M; Luo H; Fang Z; Yang C; Xie L; Jiang L Eur J Pediatr; 2023 Feb; 182(2):825-836. PubMed ID: 36484864 [TBL] [Abstract][Full Text] [Related]
13. Alternating hemiplegia of childhood: new diagnostic options. Gergont A; Kaciński M Neurol Neurochir Pol; 2014; 48(2):130-5. PubMed ID: 24821639 [TBL] [Abstract][Full Text] [Related]
14. Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases. Boonsimma P; Michael Gasser M; Netbaramee W; Wechapinan T; Srichomthong C; Ittiwut C; Wagner M; Krenn M; Zimprich F; Abicht A; Biskup S; Roser T; Borggraefe I; Suphapeetiporn K; Shotelersuk V Gene; 2020 Jul; 749():144709. PubMed ID: 32339621 [TBL] [Abstract][Full Text] [Related]
15. [Alternating Hemiplegia of Childhood associated with a pathogenic variant of the ATP1A3 gene]. Sandoval F; López F Andes Pediatr; 2022 Feb; 93(1):117-122. PubMed ID: 35506785 [TBL] [Abstract][Full Text] [Related]
16. Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2. Pavone P; Pappalardo XG; Incorpora G; Falsaperla R; Marino SD; Corsello G; Parano E; Ruggieri M Eur J Med Genet; 2020 Aug; 63(8):103957. PubMed ID: 32454213 [TBL] [Abstract][Full Text] [Related]
17. Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype. Jaffer F; Avbersek A; Vavassori R; Fons C; Campistol J; Stagnaro M; De Grandis E; Veneselli E; Rosewich H; Gianotta M; Zucca C; Ragona F; Granata T; Nardocci N; Mikati M; Helseth AR; Boelman C; Minassian BA; Johns S; Garry SI; Scheffer IE; Gourfinkel-An I; Carrilho I; Aylett SE; Parton M; Hanna MG; Houlden H; Neville B; Kurian MA; Novy J; Sander JW; Lambiase PD; Behr ER; Schyns T; Arzimanoglou A; Cross JH; Kaski JP; Sisodiya SM Brain; 2015 Oct; 138(Pt 10):2859-74. PubMed ID: 26297560 [TBL] [Abstract][Full Text] [Related]