136 related articles for article (PubMed ID: 21869492)
1. Genotyping and prenatal diagnosis of a large spinocerebellar ataxia pedigree in northeastern China.
Cao DH; Liu XL; Qiu GB
J Genet; 2011 Aug; 90(2):369-72. PubMed ID: 21869492
[No Abstract] [Full Text] [Related]
2. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
Jiang M; Jin CL; Lin CK; Qiu GR; Liu ZL; Wang CX; Sun KL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
[TBL] [Abstract][Full Text] [Related]
3. [Hereditary spinocerebellar ataxia--a family pedigree with SCA3 gene mutation].
Jiang XH; Ye L; Fu Y; Yu HZ; Yu GP; Zhao YJ; Ning G; Li XY
Zhonghua Yi Xue Za Zhi; 2005 Mar; 85(12):848-9. PubMed ID: 15949406
[No Abstract] [Full Text] [Related]
4. [Molecular and prenatal diagnosis of a pedigree with spinocerebellar ataxia].
Cao DH; Ren MH; Liu XL; Jin CL; Meng ZY; Qiu GB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):320-3. PubMed ID: 20533274
[TBL] [Abstract][Full Text] [Related]
5. Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family.
França MC; Calcagnotto ME; da Costa JC; Lopes-Cendes I
Mov Disord; 2006 Jul; 21(7):1051-3. PubMed ID: 16628604
[TBL] [Abstract][Full Text] [Related]
6. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Tang JG
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct; 31(5):702-5. PubMed ID: 17062934
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
[TBL] [Abstract][Full Text] [Related]
9. Machado-Joseph disease and other rare spinocerebellar ataxias.
Matilla-Dueñas A
Adv Exp Med Biol; 2012; 724():172-88. PubMed ID: 22411243
[TBL] [Abstract][Full Text] [Related]
10. Long-range PCR for the diagnosis of spinocerebellar ataxia type 10.
Kurosaki T; Matsuura T; Ohno K; Ueda S
Neurogenetics; 2008 May; 9(2):151-2. PubMed ID: 18197441
[No Abstract] [Full Text] [Related]
11. Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications.
Laffita-Mesa JM; Bauer PO; Kourí V; Peña Serrano L; Roskams J; Almaguer Gotay D; Montes Brown JC; Martínez Rodríguez PA; González-Zaldívar Y; Almaguer Mederos L; Cuello-Almarales D; Aguiar Santiago J
Hum Genet; 2012 Apr; 131(4):625-38. PubMed ID: 22037902
[TBL] [Abstract][Full Text] [Related]
12. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
13. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
Sułek-Piatkowska A; Zdzienicka E; Raczyńska-Rakowicz M; Krysa W; Rajkiewicz M; Szirkowiec W; Zaremba J
Neurol Neurochir Pol; 2010; 44(3):238-45. PubMed ID: 20625959
[TBL] [Abstract][Full Text] [Related]
14. SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.
Krishna N; Mohan S; Yashavantha BS; Rammurthy A; Kiran Kumar HB; Mittal U; Tyagi S; Mukerji M; Jain S; Pal PK; Purushottam M
Indian J Med Res; 2007 Nov; 126(5):465-70. PubMed ID: 18160752
[TBL] [Abstract][Full Text] [Related]
15. Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12.
Srivastava AK; Choudhry S; Gopinath MS; Roy S; Tripathi M; Brahmachari SK; Jain S
Ann Neurol; 2001 Dec; 50(6):796-800. PubMed ID: 11761478
[TBL] [Abstract][Full Text] [Related]
16. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
17. Hereditary ataxias.
Evidente VG; Gwinn-Hardy KA; Caviness JN; Gilman S
Mayo Clin Proc; 2000 May; 75(5):475-90. PubMed ID: 10807077
[TBL] [Abstract][Full Text] [Related]
18. [A pedigree affected with spinocerebellar ataxia type III].
Geng Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):463-464. PubMed ID: 28604978
[No Abstract] [Full Text] [Related]
19. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
Mori M; Adachi Y; Kusumi M; Nakashima K
Neuroepidemiology; 2001 May; 20(2):144-9. PubMed ID: 11359084
[TBL] [Abstract][Full Text] [Related]
20. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.
Dorschner MO; Barden D; Stephens K
J Mol Diagn; 2002 May; 4(2):108-13. PubMed ID: 11986402
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]