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8. [Spinocerebellar ataxia type 8(SCA 8)]. Izumi Y; Maruyama H; Kawakami H No To Shinkei; 2001 Jan; 53(1):34-40. PubMed ID: 11211728 [No Abstract] [Full Text] [Related]
9. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10. Raskin S; Ashizawa T; Teive HA; Arruda WO; Fang P; Gao R; White MC; Werneck LC; Roa B Arch Neurol; 2007 Apr; 64(4):591-4. PubMed ID: 17420323 [TBL] [Abstract][Full Text] [Related]
10. 14-3-3 proteins and spinocerebellar ataxia type 1: from molecular interaction to human neuropathology. Umahara T; Uchihara T Cerebellum; 2010 Jun; 9(2):183-9. PubMed ID: 20155408 [TBL] [Abstract][Full Text] [Related]
11. Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7. Oh AK; Jacobson KM; Jen JC; Baloh RW Ann Neurol; 2001 Jun; 49(6):801-4. PubMed ID: 11409434 [TBL] [Abstract][Full Text] [Related]
12. Similarities between spinocerebellar ataxia type 7 (SCA7) cell models and human brain: proteins recruited in inclusions and activation of caspase-3. Zander C; Takahashi J; El Hachimi KH; Fujigasaki H; Albanese V; Lebre AS; Stevanin G; Duyckaerts C; Brice A Hum Mol Genet; 2001 Oct; 10(22):2569-79. PubMed ID: 11709544 [TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia type 7. Martin JJ Handb Clin Neurol; 2012; 103():475-91. PubMed ID: 21827908 [TBL] [Abstract][Full Text] [Related]
14. Spinocerebellar ataxia type 11. Giunti P; Houlden H; Gardner-Thorpe C; Worth PF; Johnson J; Hilton DA; Revesz T; Davis MB; Wood NW Handb Clin Neurol; 2012; 103():521-34. PubMed ID: 21827911 [No Abstract] [Full Text] [Related]
15. Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10. Alonso I; Jardim LB; Artigalas O; Saraiva-Pereira ML; Matsuura T; Ashizawa T; Sequeiros J; Silveira I Neurology; 2006 May; 66(10):1602-4. PubMed ID: 16717236 [No Abstract] [Full Text] [Related]
16. 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]
17. Amino acids in a region of ataxin-1 outside of the polyglutamine tract influence the course of disease in SCA1 transgenic mice. Skinner PJ; Vierra-Green CA; Emamian E; Zoghbi HY; Orr HT Neuromolecular Med; 2002; 1(1):33-42. PubMed ID: 12025814 [TBL] [Abstract][Full Text] [Related]
18. The spinocerebellar ataxias: clinical aspects and molecular genetics. Matilla-Dueñas A; Corral-Juan M; Volpini V; Sanchez I Adv Exp Med Biol; 2012; 724():351-74. PubMed ID: 22411256 [TBL] [Abstract][Full Text] [Related]
19. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier? Matsuura T; Fang P; Pearson CE; Jayakar P; Ashizawa T; Roa BB; Nelson DL Am J Hum Genet; 2006 Jan; 78(1):125-9. PubMed ID: 16385455 [TBL] [Abstract][Full Text] [Related]
20. Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration. Garden GA; La Spada AR Cerebellum; 2008; 7(2):138-49. PubMed ID: 18418675 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]