207 related articles for article (PubMed ID: 24983657)
1. Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress.
Sugimoto H; Ikeda K; Kawakami K
Behav Brain Res; 2014 Oct; 272():100-10. PubMed ID: 24983657
[TBL] [Abstract][Full Text] [Related]
2. Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.
DeAndrade MP; Yokoi F; van Groen T; Lingrel JB; Li Y
Behav Brain Res; 2011 Jan; 216(2):659-65. PubMed ID: 20850480
[TBL] [Abstract][Full Text] [Related]
3. [A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].
Zhang CL; Yin F; He F; Gai N; Shi ZQ; Peng J
Zhonghua Er Ke Za Zhi; 2017 Apr; 55(4):288-293. PubMed ID: 28441826
[No Abstract] [Full Text] [Related]
4. Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice.
Ikeda K; Satake S; Onaka T; Sugimoto H; Takeda N; Imoto K; Kawakami K
J Physiol; 2013 Jul; 591(13):3433-49. PubMed ID: 23652595
[TBL] [Abstract][Full Text] [Related]
5. Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain.
Bøttger P; Tracz Z; Heuck A; Nissen P; Romero-Ramos M; Lykke-Hartmann K
J Comp Neurol; 2011 Feb; 519(2):376-404. PubMed ID: 21165980
[TBL] [Abstract][Full Text] [Related]
6. Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings.
Oblak AL; Hagen MC; Sweadner KJ; Haq I; Whitlow CT; Maldjian JA; Epperson F; Cook JF; Stacy M; Murrell JR; Ozelius LJ; Brashear A; Ghetti B
Acta Neuropathol; 2014 Jul; 128(1):81-98. PubMed ID: 24803225
[TBL] [Abstract][Full Text] [Related]
7. The Expanding Phenotypic Spectrums Associated with ATP1A3 Mutation in a Family with Rapid-Onset Dystonia Parkinsonism.
Yuan Y; Ran L; Lei L; Zhu H; Zhu X; Chen H
Neurodegener Dis; 2020; 20(2-3):84-89. PubMed ID: 33326973
[TBL] [Abstract][Full Text] [Related]
8. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Brashear A; Dobyns WB; de Carvalho Aguiar P; Borg M; Frijns CJ; Gollamudi S; Green A; Guimaraes J; Haake BC; Klein C; Linazasoro G; Münchau A; Raymond D; Riley D; Saunders-Pullman R; Tijssen MA; Webb D; Zaremba J; Bressman SB; Ozelius LJ
Brain; 2007 Mar; 130(Pt 3):828-35. PubMed ID: 17282997
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
de Carvalho Aguiar P; Sweadner KJ; Penniston JT; Zaremba J; Liu L; Caton M; Linazasoro G; Borg M; Tijssen MA; Bressman SB; Dobyns WB; Brashear A; Ozelius LJ
Neuron; 2004 Jul; 43(2):169-75. PubMed ID: 15260953
[TBL] [Abstract][Full Text] [Related]
11. Decreased neuronal Na+, K+ -ATPase activity in Atp1a3 heterozygous mice increases susceptibility to depression-like endophenotypes by chronic variable stress.
Kirshenbaum GS; Saltzman K; Rose B; Petersen J; Vilsen B; Roder JC
Genes Brain Behav; 2011 Jul; 10(5):542-50. PubMed ID: 21418141
[TBL] [Abstract][Full Text] [Related]
12. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
Sweney MT; Newcomb TM; Swoboda KJ
Pediatr Neurol; 2015 Jan; 52(1):56-64. PubMed ID: 25447930
[TBL] [Abstract][Full Text] [Related]
13. Implantation of Osmotic Pumps and Induction of Stress to Establish a Symptomatic, Pharmacological Mouse Model for DYT/PARK-ATP1A3 Dystonia.
Rauschenberger L; Knorr S; Volkmann J; Ip CW
J Vis Exp; 2020 Sep; (163):. PubMed ID: 32986028
[TBL] [Abstract][Full Text] [Related]
14. Striatal dopaminergic dysregulation and dystonia-like movements induced by sensorimotor stress in a pharmacological mouse model of rapid-onset dystonia-parkinsonism.
Rauschenberger L; Knorr S; Al-Zuraiqi Y; Tovote P; Volkmann J; Ip CW
Exp Neurol; 2020 Jan; 323():113109. PubMed ID: 31712125
[TBL] [Abstract][Full Text] [Related]
15. ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.
Lee JY; Gollamudi S; Ozelius LJ; Kim JY; Jeon BS
Mov Disord; 2007 Sep; 22(12):1808-9. PubMed ID: 17595045
[TBL] [Abstract][Full Text] [Related]
16. The neural substrates of rapid-onset Dystonia-Parkinsonism.
Calderon DP; Fremont R; Kraenzlin F; Khodakhah K
Nat Neurosci; 2011 Mar; 14(3):357-65. PubMed ID: 21297628
[TBL] [Abstract][Full Text] [Related]
17. A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment.
Liu Y; Lu Y; Zhang X; Xie S; Wang T; Wu T; Wang C
BMC Neurol; 2016 Nov; 16(1):218. PubMed ID: 27835968
[TBL] [Abstract][Full Text] [Related]
18. Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
Haq IU; Snively BM; Sweadner KJ; Suerken CK; Cook JF; Ozelius LJ; Miller C; McCall WV; Whitlow CT; Brashear A
Mov Disord; 2019 Oct; 34(10):1528-1536. PubMed ID: 31361359
[TBL] [Abstract][Full Text] [Related]
19. ATP1A3 Mutation in Adult Rapid-Onset Ataxia.
Sweadner KJ; Toro C; Whitlow CT; Snively BM; Cook JF; Ozelius LJ; Markello TC; Brashear A
PLoS One; 2016; 11(3):e0151429. PubMed ID: 26990090
[TBL] [Abstract][Full Text] [Related]
20. Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism.
Fremont R; Tewari A; Khodakhah K
Neurobiol Dis; 2015 Oct; 82():200-212. PubMed ID: 26093171
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]