These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
129 related articles for article (PubMed ID: 20739808)
1. Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7. Han Y; Deng B; Liu M; Jiang J; Wu S; Guan Y Neurol India; 2010; 58(4):622-6. PubMed ID: 20739808 [TBL] [Abstract][Full Text] [Related]
2. Clinical and genetic study of spinocerebellar ataxia type 7 in East Asian population. Han Y; Yu L; Zheng HM; Guan YT Chin Med J (Engl); 2010 Aug; 123(16):2274-8. PubMed ID: 20819679 [TBL] [Abstract][Full Text] [Related]
3. Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7. Katagiri S; Hayashi T; Takeuchi T; Yamada H; Gekka T; Kawabe K; Kurita A; Tsuneoka H Doc Ophthalmol; 2015 Jun; 130(3):189-95. PubMed ID: 25643591 [TBL] [Abstract][Full Text] [Related]
4. Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds. Gu W; Wang Y; Liu X; Zhou B; Zhou Y; Wang G Arch Neurol; 2000 Oct; 57(10):1513-8. PubMed ID: 11030806 [TBL] [Abstract][Full Text] [Related]
5. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family. Martin J; Van Regemorter N; Del-Favero J; Löfgren A; Van Broeckhoven C J Neurol Sci; 1999 Sep; 168(1):37-46. PubMed ID: 10500272 [TBL] [Abstract][Full Text] [Related]
6. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan. Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863 [TBL] [Abstract][Full Text] [Related]
7. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia. Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population. Faruq M; Srivastava AK; Singh S; Gupta R; Dada T; Garg A; Behari M; Mukerji M Indian J Med Res; 2015 Feb; 141(2):187-98. PubMed ID: 25900954 [TBL] [Abstract][Full Text] [Related]
10. Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot. Hsieh M; Lin SJ; Chen JF; Lin HM; Hsiao KM; Li SY; Li C; Tsai CJ J Neurol; 2000 Aug; 247(8):623-9. PubMed ID: 11041330 [TBL] [Abstract][Full Text] [Related]
11. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). David G; Dürr A; Stevanin G; Cancel G; Abbas N; Benomar A; Belal S; Lebre AS; Abada-Bendib M; Grid D; Holmberg M; Yahyaoui M; Hentati F; Chkili T; Agid Y; Brice A Hum Mol Genet; 1998 Feb; 7(2):165-70. PubMed ID: 9425222 [TBL] [Abstract][Full Text] [Related]
12. Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation. Johansson J; Forsgren L; Sandgren O; Brice A; Holmgren G; Holmberg M Hum Mol Genet; 1998 Feb; 7(2):171-6. PubMed ID: 9425223 [TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia type 7: report of a new Italian family. Italiano D; Tarantino P; De Marco EV; Calabrò RS; Bramanti P; Quattrone A; Annesi G Intern Med; 2012; 51(20):2953-5. PubMed ID: 23064575 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. Massive CAG repeat expansion and somatic instability in maternally transmitted infantile spinocerebellar ataxia type 7. Trang H; Stanley SY; Thorner P; Faghfoury H; Schulze A; Hawkins C; Pearson CE; Yoon G JAMA Neurol; 2015 Feb; 72(2):219-23. PubMed ID: 25506882 [TBL] [Abstract][Full Text] [Related]
17. Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias. Albuquerque MV; Pedroso JL; Braga Neto P; Barsottini OG Arq Neuropsiquiatr; 2015 Jan; 73(1):18-21. PubMed ID: 25608122 [TBL] [Abstract][Full Text] [Related]
18. Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case. Ouchi H; Ishiguro H; Shibano K; Hara K; Sugawara M; Enomoto K; Miyata H Neuropathology; 2023 Apr; 43(2):164-175. PubMed ID: 36168676 [TBL] [Abstract][Full Text] [Related]
19. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han]. Wang J; Xu Q; Lei L; Shen L; Jiang H; Li X; Zhou Y; Yi J; Zhou J; Yan X; Pan Q; Xia K; Tang B Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):620-5. PubMed ID: 19953482 [TBL] [Abstract][Full Text] [Related]