165 related articles for article (PubMed ID: 33222902)
1. 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]
2. [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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Rapid-onset dystonia-parkinsonism with ATP1A3 mutation and left lower limb paroxysmal dystonia.
Nomura S; Kashiwagi M; Tanabe T; Oba C; Yanagi K; Kaname T; Okamoto N; Ashida A
Brain Dev; 2021 Apr; 43(4):566-570. PubMed ID: 33451880
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.
Wilcox R; Brænne I; Brüggemann N; Winkler S; Wiegers K; Bertram L; Anderson T; Lohmann K
J Neurol; 2015 Jan; 262(1):187-93. PubMed ID: 25359261
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Auditory-Perceptual Evaluation of Deep Brain Stimulation on Voice and Speech in Patients With Dystonia.
Finger ME; Siddiqui MS; Morris AK; Ruckart KW; Wright SC; Haq IU; Madden LL
J Voice; 2020 Jul; 34(4):636-644. PubMed ID: 30879706
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Assessment of Dysphonia in Children with Pompe Disease Using Auditory-Perceptual and Acoustic/Physiologic Methods.
Crisp KD; Neel AT; Amarasekara S; Marcus J; Nichting G; Korlimarla A; Kishnani PS; Jones HN
J Clin Med; 2021 Aug; 10(16):. PubMed ID: 34441913
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]