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.
105 related articles for article (PubMed ID: 7669409)
41. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging]. Kojima S Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328 [TBL] [Abstract][Full Text] [Related]
42. Nucleotide sequence of the SAC2 gene of Saccharomyces cerevisiae. Kölling R; Lee A; Chen EY; Botstein D Yeast; 1994 Sep; 10(9):1211-6. PubMed ID: 7754710 [TBL] [Abstract][Full Text] [Related]
43. [Olivocerebellar atrophy of the Holmes type in 2 generations]. Klaus H; Haug HJ Psychiatr Prax; 1994 Jul; 21(4):160-1. PubMed ID: 7938327 [TBL] [Abstract][Full Text] [Related]
44. [The contribution of molecular genetics to the nosology and diagnosis of neurological disorders of childhood]. Aicardi J Rev Neurol; 1999 Jan 1-15; 28(1):1-4. PubMed ID: 10101756 [TBL] [Abstract][Full Text] [Related]
45. [Comparison between MRI and 3D-SSP in olivopontocerebellar atrophy and cortical cerebellar atrophy]. Hamaguchi H; Kanda F; Hosaka K; Fujii M; Chihara K Rinsho Shinkeigaku; 2004; 44(4-5):263-7. PubMed ID: 15287507 [TBL] [Abstract][Full Text] [Related]
46. [Genes for human brain diseases--dentatorubral-pallidoluysian atrophy]. Naito H; Tsuji S Tanpakushitsu Kakusan Koso; 1995 Apr; 40(6):829-33. PubMed ID: 7754068 [No Abstract] [Full Text] [Related]
47. Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy. Duvoisin RC; Nicklas WJ; Ritchie V; Sage J; Chokroverty S J Neurol Neurosurg Psychiatry; 1988 Dec; 51(12):1508-11. PubMed ID: 3221218 [TBL] [Abstract][Full Text] [Related]
48. Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680 [TBL] [Abstract][Full Text] [Related]
49. Changes in vitamin E concentration in red blood cells and plasma of patients with olivopontocerebellar ataxia within the Schut-Swier kindred. Vatassery GT; Schut LJ J Am Coll Nutr; 1987 Apr; 6(2):151-6. PubMed ID: 3473124 [TBL] [Abstract][Full Text] [Related]
50. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. Chung MY; Ranum LP; Duvick LA; Servadio A; Zoghbi HY; Orr HT Nat Genet; 1993 Nov; 5(3):254-8. PubMed ID: 8275090 [TBL] [Abstract][Full Text] [Related]
51. Cerebellar ataxia, dystonia, and tremor within a family: variable phenotypes of a single genetic disorder? Adler CH; Wrabetz L; Brin MF; Hurtig HI Mov Disord; 1994 Mar; 9(2):155-60. PubMed ID: 8196675 [TBL] [Abstract][Full Text] [Related]
53. Chilean population data on ten PCR-based loci. Jorquera H; Budowle B J Forensic Sci; 1998 Jan; 43(1):171-3. PubMed ID: 9456538 [TBL] [Abstract][Full Text] [Related]
55. Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1. Mascalchi M; Tosetti M; Plasmati R; Bianchi MC; Tessa C; Salvi F; Frontali M; Valzania F; Bartolozzi C; Tassinari CA Ann Neurol; 1998 Feb; 43(2):244-52. PubMed ID: 9485066 [TBL] [Abstract][Full Text] [Related]
56. [Spinocerebellar ataxia: advances in genetic research and its clinical implication]. Sasaki H Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358 [TBL] [Abstract][Full Text] [Related]