175 related articles for article (PubMed ID: 19380697)
1. Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.
Kim JY; Kim SY; Kim JM; Kim YK; Yoon KY; Kim JY; Lee BC; Kim JS; Paek SH; Park SS; Kim SE; Jeon BS
Neurology; 2009 Apr; 72(16):1385-9. PubMed ID: 19380697
[TBL] [Abstract][Full Text] [Related]
2. Relative contribution of SCA2, SCA3 and SCA17 in Korean patients with parkinsonism and ataxia.
Yun JY; Lee WW; Kim HJ; Kim JS; Kim JM; Kim HJ; Kim SY; Kim JY; Park SS; Kim YK; Kim SE; Jeon BS
Parkinsonism Relat Disord; 2011 Jun; 17(5):338-42. PubMed ID: 21334959
[TBL] [Abstract][Full Text] [Related]
3. Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism.
Kim JM; Hong S; Kim GP; Choi YJ; Kim YK; Park SS; Kim SE; Jeon BS
Arch Neurol; 2007 Oct; 64(10):1510-8. PubMed ID: 17923635
[TBL] [Abstract][Full Text] [Related]
4. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
5. Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).
Hübner J; Sprenger A; Klein C; Hagenah J; Rambold H; Zühlke C; Kömpf D; Rolfs A; Kimmig H; Helmchen C
Neurology; 2007 Sep; 69(11):1160-8. PubMed ID: 17846415
[TBL] [Abstract][Full Text] [Related]
6. Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.
Salvatore E; Varrone A; Sansone V; Nolano M; Bruni AC; De Rosa A; Santoro L; Pappatà S; Filla A; De Michele G
Mov Disord; 2006 Jun; 21(6):872-5. PubMed ID: 16532453
[TBL] [Abstract][Full Text] [Related]
7. Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers.
Ceravolo R; Antonini A; Volterrani D; Rossi C; Goldwurm S; Di Maria E; Kiferle L; Bonuccelli U; Murri L
Neurology; 2005 Dec; 65(12):1971-3. PubMed ID: 16380622
[TBL] [Abstract][Full Text] [Related]
8. Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.
Lu CS; Wu Chou YH; Yen TC; Tsai CH; Chen RS; Chang HC
Mov Disord; 2002 Sep; 17(5):1046-51. PubMed ID: 12360557
[TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism.
Krygowska-Wajs A; Kachergus JM; Hulihan MM; Farrer MJ; Searcy JA; Booij J; Berendse HW; Wolters ECh; Wszolek ZK
J Neural Transm (Vienna); 2005 Nov; 112(11):1487-502. PubMed ID: 15785861
[TBL] [Abstract][Full Text] [Related]
10. The Pathogenic Role of Low Range Repeats in SCA17.
Shin JH; Park H; Ehm GH; Lee WW; Yun JY; Kim YE; Lee JY; Kim HJ; Kim JM; Jeon BS; Park SS
PLoS One; 2015; 10(8):e0135275. PubMed ID: 26267067
[TBL] [Abstract][Full Text] [Related]
11. Mutation at the SCA17 locus is not a common cause of parkinsonism.
Hernandez D; Hanson M; Singleton A; Gwinn-Hardy K; Freeman J; Ravina B; Doheny D; Gallardo M; Weiser R; Hardy J; Singleton A
Parkinsonism Relat Disord; 2003 Aug; 9(6):317-20. PubMed ID: 12853230
[TBL] [Abstract][Full Text] [Related]
12. Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT.
Mäkinen E; Joutsa J; Jaakkola E; Noponen T; Johansson J; Pitkonen M; Levo R; Mertsalmi T; Scheperjans F; Kaasinen V
J Neurol; 2019 Apr; 266(4):826-834. PubMed ID: 30687897
[TBL] [Abstract][Full Text] [Related]
13. No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.
Schöls L; Reimold M; Seidel K; Globas C; Brockmann K; Hauser TK; Auburger G; Bürk K; den Dunnen W; Reischl G; Korf HW; Brunt ER; Rüb U
Brain; 2015 Nov; 138(Pt 11):3316-26. PubMed ID: 26362908
[TBL] [Abstract][Full Text] [Related]
14. Decreased dopamine transporter binding in Machado-Joseph disease.
Yen TC; Lu CS; Tzen KY; Wey SP; Chou YH; Weng YH; Kao PF; Ting G
J Nucl Med; 2000 Jun; 41(6):994-8. PubMed ID: 10855623
[TBL] [Abstract][Full Text] [Related]
15. The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family.
Lu CS; Chang HC; Kuo PC; Liu YL; Wu WS; Weng YH; Yen TC; Chou YH
Parkinsonism Relat Disord; 2004 Aug; 10(6):369-73. PubMed ID: 15261879
[TBL] [Abstract][Full Text] [Related]
16. SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications.
Chen CM; Lee LC; Soong BW; Fung HC; Hsu WC; Lin PY; Huang HJ; Chen FL; Lin CY; Lee-Chen GJ; Wu YR
Clin Chim Acta; 2010 Mar; 411(5-6):375-80. PubMed ID: 20004653
[TBL] [Abstract][Full Text] [Related]
17. Effects of C825T polymorphism of the GNB3 gene on availability of dopamine transporter in healthy volunteers--a SPECT study.
Chen PS; Yeh TL; Lee IH; Lin CB; Tsai HC; Chen KC; Chiu NT; Yao WJ; Yang YK; Chou YH
Neuroimage; 2011 Jun; 56(3):1526-30. PubMed ID: 21371559
[TBL] [Abstract][Full Text] [Related]
18. Trinucleotide repeat expansion of TATA-binding protein gene associated with Parkinson's disease: A Thai multicenter study.
Choubtum L; Witoonpanich P; Kulkantrakorn K; Hanchaiphiboolkul S; Pongpakdee S; Tiamkao S; Pulkes T
Parkinsonism Relat Disord; 2016 Jul; 28():146-9. PubMed ID: 27172828
[TBL] [Abstract][Full Text] [Related]
19. Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes.
Zühlke C; Dalski A; Schwinger E; Finckh U
BMC Med Genet; 2005 Jul; 6():27. PubMed ID: 15989694
[TBL] [Abstract][Full Text] [Related]
20. Higher striatal dopamine transporters in euthymic patients with bipolar disorder: a SPECT study with [Tc] TRODAT-1.
Chang TT; Yeh TL; Chiu NT; Chen PS; Huang HY; Yang YK; Lee IH; Lu RB
Bipolar Disord; 2010 Feb; 12(1):102-6. PubMed ID: 20148872
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
