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2. Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood. Kirshenbaum GS; Dachtler J; Roder JC; Clapcote SJ Neurogenetics; 2016 Jan; 17(1):57-63. PubMed ID: 26463346 [TBL] [Abstract][Full Text] [Related]
3. Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood. Kirshenbaum GS; Idris NF; Dachtler J; Roder JC; Clapcote SJ J Neurogenet; 2016 Mar; 30(1):42-9. PubMed ID: 27276195 [TBL] [Abstract][Full Text] [Related]
4. A functional correlate of severity in alternating hemiplegia of childhood. Li M; Jazayeri D; Corry B; McSweeney KM; Heinzen EL; Goldstein DB; Petrou S Neurobiol Dis; 2015 May; 77():88-93. PubMed ID: 25681536 [TBL] [Abstract][Full Text] [Related]
5. Alternating Hemiplegia of Childhood mutations have a differential effect on Na(+),K(+)-ATPase activity and ouabain binding. Weigand KM; Messchaert M; Swarts HG; Russel FG; Koenderink JB Biochim Biophys Acta; 2014 Jul; 1842(7):1010-6. PubMed ID: 24631656 [TBL] [Abstract][Full Text] [Related]
6. Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation. Kirshenbaum GS; Dachtler J; Roder JC; Clapcote SJ Behav Neurosci; 2015 Dec; 129(6):822-31. PubMed ID: 26501181 [TBL] [Abstract][Full Text] [Related]
7. Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity. Lazarov E; Hillebrand M; Schröder S; Ternka K; Hofhuis J; Ohlenbusch A; Barrantes-Freer A; Pardo LA; Fruergaard MU; Nissen P; Brockmann K; Gärtner J; Rosewich H Neurobiol Dis; 2020 Sep; 143():105012. PubMed ID: 32653672 [TBL] [Abstract][Full Text] [Related]
8. Novel E815K knock-in mouse model of alternating hemiplegia of childhood. Helseth AR; Hunanyan AS; Adil S; Linabarger M; Sachdev M; Abdelnour E; Arehart E; Szabo M; Richardson J; Wetsel WC; Hochgeschwender U; Mikati MA Neurobiol Dis; 2018 Nov; 119():100-112. PubMed ID: 30071271 [TBL] [Abstract][Full Text] [Related]
9. ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood--Potential target of treatment? Wong VC; Kwong AK Brain Dev; 2015 Oct; 37(9):907-10. PubMed ID: 25662428 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Cognitive deficits caused by a disease-mutation in the α3 Na(+)/K(+)-ATPase isoform. Holm TH; Isaksen TJ; Glerup S; Heuck A; Bøttger P; Füchtbauer EM; Nedergaard S; Nyengaard JR; Andreasen M; Nissen P; Lykke-Hartmann K Sci Rep; 2016 Aug; 6():31972. PubMed ID: 27549929 [TBL] [Abstract][Full Text] [Related]
12. Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. Panagiotakaki E; Tiziano FD; Mikati MA; Vijfhuizen LS; Nicole S; Lesca G; Abiusi E; Novelli A; Di Pietro L; ; ; Harder AVE; Walley NM; De Grandis E; Poulat AL; Portes VD; Lépine A; Nassogne MC; Arzimanoglou A; Vavassori R; Koenderink J; Thompson CH; George AL; Gurrieri F; van den Maagdenberg AMJM; Heinzen EL Eur J Hum Genet; 2024 Feb; 32(2):224-231. PubMed ID: 38097767 [TBL] [Abstract][Full Text] [Related]
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