These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 26501181)

  • 1. 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]  

  • 2. Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.
    Kirshenbaum GS; Dawson N; Mullins JG; Johnston TH; Drinkhill MJ; Edwards IJ; Fox SH; Pratt JA; Brotchie JM; Roder JC; Clapcote SJ
    PLoS One; 2013; 8(3):e60141. PubMed ID: 23527305
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 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. Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.
    Hunanyan AS; Fainberg NA; Linabarger M; Arehart E; Leonard AS; Adil SM; Helseth AR; Swearingen AK; Forbes SL; Rodriguiz RM; Rhodes T; Yao X; Kibbi N; Hochman DW; Wetsel WC; Hochgeschwender U; Mikati MA
    Epilepsia; 2015 Jan; 56(1):82-93. PubMed ID: 25523819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation status.
    Hoei-Hansen CE; Dali CÍ; Lyngbye TJ; Duno M; Uldall P
    Eur J Paediatr Neurol; 2014 Jan; 18(1):50-4. PubMed ID: 24100174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Early-life seizures result in deficits in social behavior and learning.
    Lugo JN; Swann JW; Anderson AE
    Exp Neurol; 2014 Jun; 256():74-80. PubMed ID: 24685665
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cognitive, adaptive, and behavioral profiles and management of alternating hemiplegia of childhood.
    Jasien JM; Bonner M; D'alli R; Prange L; Mclean M; Sachdev M; Uchitel J; Ricano J; Smith B; Mikati MA
    Dev Med Child Neurol; 2019 May; 61(5):547-554. PubMed ID: 30362107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhood.
    Simmons CQ; Thompson CH; Cawthon BE; Westlake G; Swoboda KJ; Kiskinis E; Ess KC; George AL
    Neurobiol Dis; 2018 Jul; 115():29-38. PubMed ID: 29567111
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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. Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
    Rosewich H; Thiele H; Ohlenbusch A; Maschke U; Altmüller J; Frommolt P; Zirn B; Ebinger F; Siemes H; Nürnberg P; Brockmann K; Gärtner J
    Lancet Neurol; 2012 Sep; 11(9):764-73. PubMed ID: 22850527
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficiency in Na,K-ATPase alpha isoform genes alters spatial learning, motor activity, and anxiety in mice.
    Moseley AE; Williams MT; Schaefer TL; Bohanan CS; Neumann JC; Behbehani MM; Vorhees CV; Lingrel JB
    J Neurosci; 2007 Jan; 27(3):616-26. PubMed ID: 17234593
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients.
    Ishii A; Saito Y; Mitsui J; Ishiura H; Yoshimura J; Arai H; Yamashita S; Kimura S; Oguni H; Morishita S; Tsuji S; Sasaki M; Hirose S
    PLoS One; 2013; 8(2):e56120. PubMed ID: 23409136
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotype.
    Snow JP; Westlake G; Klofas LK; Jeon S; Armstrong LC; Swoboda KJ; George AL; Ess KC
    Neurobiol Dis; 2020 Jul; 141():104881. PubMed ID: 32348881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.