219 related articles for article (PubMed ID: 10668721)
21. Imperfect CAG repeats form diverse structures in SCA1 transcripts.
Sobczak K; Krzyzosiak WJ
J Biol Chem; 2004 Oct; 279(40):41563-72. PubMed ID: 15292212
[TBL] [Abstract][Full Text] [Related]
22. Absence of spinocerebellar ataxia type 3/Machado-Joseph disease within ataxic patients in the Czech population.
Bauer PO; Zumrova A; Matoska V; Marikova T; Krilova S; Boday A; Singh B; Goetz P
Eur J Neurol; 2005 Nov; 12(11):851-7. PubMed ID: 16241973
[TBL] [Abstract][Full Text] [Related]
23. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.
Netravathi M; Pal PK; Purushottam M; Thennarasu K; Mukherjee M; Jain S
J Neurol Sci; 2009 Feb; 277(1-2):83-6. PubMed ID: 19049837
[TBL] [Abstract][Full Text] [Related]
24. Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of disease.
Yiş U; Dirik E; Kurul SH; Eken AG; Başak AN
Cerebellum; 2009 Jun; 8(2):127-9. PubMed ID: 19023636
[TBL] [Abstract][Full Text] [Related]
25. Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17.
Gao R; Matsuura T; Coolbaugh M; Zühlke C; Nakamura K; Rasmussen A; Siciliano MJ; Ashizawa T; Lin X
Eur J Hum Genet; 2008 Feb; 16(2):215-22. PubMed ID: 18043721
[TBL] [Abstract][Full Text] [Related]
26. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
Savić D; Topisirović I; Keckarević M; Keckarević D; Major T; Culjković B; Stojković O; Rakocević-Stojanović V; Mladenović J; Todorović S; Apostolski S; Romac S
Psychiatr Genet; 2001 Dec; 11(4):201-5. PubMed ID: 11807410
[TBL] [Abstract][Full Text] [Related]
27. Late-onset SCA2: 33 CAG repeats are sufficient to cause disease.
Fernandez M; McClain ME; Martinez RA; Snow K; Lipe H; Ravits J; Bird TD; La Spada AR
Neurology; 2000 Aug; 55(4):569-72. PubMed ID: 10953195
[TBL] [Abstract][Full Text] [Related]
28. CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).
Hayes S; Turecki G; Brisebois K; Lopes-Cendes I; Gaspar C; Riess O; Ranum LP; Pulst SM; Rouleau GA
Hum Mol Genet; 2000 Jul; 9(12):1753-8. PubMed ID: 10915763
[TBL] [Abstract][Full Text] [Related]
29. Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.
Hedera P; Rainier S; Zhao XP; Schalling M; Lindblad K; Yuan QP; Ikeuchi T; Trobe J; Wald JJ; Eldevik OP; Kluin K; Fink JK
Neurology; 2002 Feb; 58(3):411-6. PubMed ID: 11839840
[TBL] [Abstract][Full Text] [Related]
30. Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years.
Yang L; Dong Y; Ma Y; Ni W; Wu ZY
Eur J Neurol; 2021 Mar; 28(3):955-964. PubMed ID: 33070405
[TBL] [Abstract][Full Text] [Related]
31. Diagnosis of Spinocerebellar Ataxias Caused by Trinucleotide Repeat Expansions.
Martindale JE
Curr Protoc Hum Genet; 2017 Jan; 92():9.30.1-9.30.22. PubMed ID: 28075481
[TBL] [Abstract][Full Text] [Related]
32. A spinocerebellar ataxia family with expanded alleles in the TATA-binding protein gene and ataxin-3 gene.
Xu Q; Li Q; Wang J; Jiang H; Shen L; Li X; Tang B
Int J Neurosci; 2010 Feb; 120(2):159-61. PubMed ID: 20199210
[TBL] [Abstract][Full Text] [Related]
33. Hereditary ataxia. An unfolded protein.
Orr HT
Lancet; 2001 Dec; 358 Suppl():S35. PubMed ID: 11784584
[No Abstract] [Full Text] [Related]
34. [Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population].
Magaña JJ; Vergara MD; Sierra-Martínez M; García-Jiménez E; Rodríguez-Antonio F; Gómez Mdel R; Valdés-Flores M; Cisneros B
Gac Med Mex; 2008; 144(5):413-8. PubMed ID: 19043961
[TBL] [Abstract][Full Text] [Related]
35. Spinocerebellar ataxia type 2 in seven Korean families: CAG trinucleotide expansion and clinical characteristics.
Kim JM; Shin S; Kim JY; Joo SI; Park SS; Kim JW; Jeon BS
J Korean Med Sci; 1999 Dec; 14(6):659-64. PubMed ID: 10642945
[TBL] [Abstract][Full Text] [Related]
36. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG
Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842
[TBL] [Abstract][Full Text] [Related]
37. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12.
Dong Y; Wu JJ; Wu ZY
Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432
[TBL] [Abstract][Full Text] [Related]
38. Spinocerebellar Ataxia Type 17 (SCA17).
Toyoshima Y; Takahashi H
Adv Exp Med Biol; 2018; 1049():219-231. PubMed ID: 29427105
[TBL] [Abstract][Full Text] [Related]
39. CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia.
Tan D; Wei C; Chen Z; Huang Y; Deng J; Li J; Liu Y; Bao X; Xu J; Hu Z; Wang S; Fan Y; Jiang Y; Wu Y; Wu Y; Wang S; Liu P; Zhang Y; Yang Z; Jiang Y; Zhang H; Hong D; Zhong N; Jiang H; Xiong H
Mov Disord; 2023 Jul; 38(7):1282-1293. PubMed ID: 37148549
[TBL] [Abstract][Full Text] [Related]
40. Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.
Shan DE; Liu RS; Sun CM; Lee SJ; Liao KK; Soong BW
Mov Disord; 2004 Nov; 19(11):1357-60. PubMed ID: 15378681
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
