238 related articles for article (PubMed ID: 24803225)
21. 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]
22. 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]
23. Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients.
Moya-Mendez ME; Madden LL; Ruckart KW; Downes KM; Cook JF; Snively BM; Brashear A; Haq IU
J Clin Neurosci; 2020 Nov; 81():133-138. PubMed ID: 33222902
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. ATP1A3-related disorders in the differential diagnosis of acute brainstem and cerebellar dysfunction.
Duat-Rodríguez A; Prochazkova M; Sebastian IP; Extremera VC; Legido MJ; Palero SR; Ortiz Cabrera NV
Eur J Paediatr Neurol; 2021 Sep; 34():105-109. PubMed ID: 34464766
[TBL] [Abstract][Full Text] [Related]
26. Cognitive impairment in rapid-onset dystonia-parkinsonism.
Cook JF; Hill DF; Snively BM; Boggs N; Suerken CK; Haq I; Stacy M; McCall WV; Ozelius LJ; Sweadner KJ; Brashear A
Mov Disord; 2014 Mar; 29(3):344-50. PubMed ID: 24436111
[TBL] [Abstract][Full Text] [Related]
27. Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.
Anselm IA; Sweadner KJ; Gollamudi S; Ozelius LJ; Darras BT
Neurology; 2009 Aug; 73(5):400-1. PubMed ID: 19652145
[No Abstract] [Full Text] [Related]
28. A novel presentation of an ATP1A3 gene mutation - case report and literature review.
Kostopoulou E; Avgeri A; Apostolou MI; Tzifas S; Dimitriou G
Eur Rev Med Pharmacol Sci; 2022 Feb; 26(4):1108-1113. PubMed ID: 35253165
[TBL] [Abstract][Full Text] [Related]
29. New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.
Barbano RL; Hill DF; Snively BM; Light LS; Boggs N; McCall WV; Stacy M; Ozelius L; Sweadner KJ; Brashear A
Parkinsonism Relat Disord; 2012 Jul; 18(6):737-41. PubMed ID: 22534615
[TBL] [Abstract][Full Text] [Related]
30. Psychiatric disorders in rapid-onset dystonia-parkinsonism.
Brashear A; Cook JF; Hill DF; Amponsah A; Snively BM; Light L; Boggs N; Suerken CK; Stacy M; Ozelius L; Sweadner KJ; McCall WV
Neurology; 2012 Sep; 79(11):1168-73. PubMed ID: 22933743
[TBL] [Abstract][Full Text] [Related]
31. Atypical presentation of rapid-onset dystonia-parkinsonism in a toddler with a novel mutation in the ATP1A3 gene.
Ganesh A; Sivakumar S; Manokaran R; Narasimhan U
BMJ Case Rep; 2021 Aug; 14(8):. PubMed ID: 34413044
[TBL] [Abstract][Full Text] [Related]
32. Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.
Tran L; Richards J; McDonald M; McConkie-Rosell A; Stong N; Jasien J; Shashi V; Mikati MA
Epileptic Disord; 2020 Feb; 22(1):103-109. PubMed ID: 32043468
[TBL] [Abstract][Full Text] [Related]
33. Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations.
Schirinzi T; Graziola F; Nicita F; Travaglini L; Stregapede F; Valeriani M; Curatolo P; Bertini E; Vigevano F; Capuano A
Cerebellum; 2018 Aug; 17(4):489-493. PubMed ID: 29397530
[TBL] [Abstract][Full Text] [Related]
34. Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.
Lacombe D; Van-Gils J; Lebrun M; Trimouille A; Michaud V; Cabet S; Chateil JF; Pedespan JM; Bar C; Lesca G
Brain Dev; 2022 Sep; 44(8):567-570. PubMed ID: 35623960
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Sporadic rapid-onset dystonia-parkinsonism presenting as Parkinson's disease.
Kamphuis DJ; Koelman H; Lees AJ; Tijssen MA
Mov Disord; 2006 Jan; 21(1):118-9. PubMed ID: 16161139
[TBL] [Abstract][Full Text] [Related]
37. ATP1A3 related disease manifesting as rapid onset dystonia-parkinsonism with prominent myoclonus and exaggerated startle.
Williams L; Waller SE; Bradley M; Lockhart A; Narayanan RK; Kumar KR; Morales Briceno H; Tchan M; Healy DG; Fung VSC
Parkinsonism Relat Disord; 2023 Dec; 117():105864. PubMed ID: 37827923
[TBL] [Abstract][Full Text] [Related]
38. Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.
Arystarkhova E; Haq IU; Luebbert T; Mochel F; Saunders-Pullman R; Bressman SB; Feschenko P; Salazar C; Cook JF; Demarest S; Brashear A; Ozelius LJ; Sweadner KJ
Neurobiol Dis; 2019 Dec; 132():104577. PubMed ID: 31425744
[TBL] [Abstract][Full Text] [Related]
39. A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism.
Wenzel GR; Lohmann K; Kühn AA
Parkinsonism Relat Disord; 2017 Apr; 37():120-122. PubMed ID: 28214263
[No Abstract] [Full Text] [Related]
40. ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
Brashear A; Mink JW; Hill DF; Boggs N; McCall WV; Stacy MA; Snively B; Light LS; Sweadner KJ; Ozelius LJ; Morrison L
Dev Med Child Neurol; 2012 Nov; 54(11):1065-7. PubMed ID: 22924536
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
