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.
273 related articles for article (PubMed ID: 9371900)
1. Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion. Matsumura R; Futamura N; Fujimoto Y; Yanagimoto S; Horikawa H; Suzumura A; Takayanagi T Neurology; 1997 Nov; 49(5):1238-43. PubMed ID: 9371900 [TBL] [Abstract][Full Text] [Related]
2. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds. Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730 [TBL] [Abstract][Full Text] [Related]
4. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6). Matsuyama Z; Kawakami H; Maruyama H; Izumi Y; Komure O; Udaka F; Kameyama M; Nishio T; Kuroda Y; Nishimura M; Nakamura S Hum Mol Genet; 1997 Aug; 6(8):1283-7. PubMed ID: 9259274 [TBL] [Abstract][Full Text] [Related]
5. Clinical and molecular features of spinocerebellar ataxia type 6. Stevanin G; Dürr A; David G; Didierjean O; Cancel G; Rivaud S; Tourbah A; Warter JM; Agid Y; Brice A Neurology; 1997 Nov; 49(5):1243-6. PubMed ID: 9371901 [TBL] [Abstract][Full Text] [Related]
6. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group. Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742 [TBL] [Abstract][Full Text] [Related]
7. A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene. Takiyama Y; Sakoe K; Namekawa M; Soutome M; Esumi E; Ogawa T; Ishikawa K; Mizusawa H; Nakano I; Nishizawa M J Neurol Sci; 1998 Jun; 158(2):141-7. PubMed ID: 9702684 [TBL] [Abstract][Full Text] [Related]
8. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population. Ikeuchi T; Takano H; Koide R; Horikawa Y; Honma Y; Onishi Y; Igarashi S; Tanaka H; Nakao N; Sahashi K; Tsukagoshi H; Inoue K; Takahashi H; Tsuji S Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480 [TBL] [Abstract][Full Text] [Related]
9. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene. Riess O; Schöls L; Bottger H; Nolte D; Vieira-Saecker AM; Schimming C; Kreuz F; Macek M; Krebsová A; Macek M Sen ; Klockgether T; Zühlke C; Laccone FA Hum Mol Genet; 1997 Aug; 6(8):1289-93. PubMed ID: 9259275 [TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular genetic study in seven Japanese families with spinocerebellar ataxia type 6. Nagai Y; Azuma T; Funauchi M; Fujita M; Umi M; Hirano M; Matsubara T; Ueno S J Neurol Sci; 1998 Apr; 157(1):52-9. PubMed ID: 9600677 [TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations. Geschwind DH; Perlman S; Figueroa KP; Karrim J; Baloh RW; Pulst SM Neurology; 1997 Nov; 49(5):1247-51. PubMed ID: 9371902 [TBL] [Abstract][Full Text] [Related]
12. Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype. Benton CS; de Silva R; Rutledge SL; Bohlega S; Ashizawa T; Zoghbi HY Neurology; 1998 Oct; 51(4):1081-6. PubMed ID: 9781533 [TBL] [Abstract][Full Text] [Related]
13. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese]. Ikeuchi T Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785 [TBL] [Abstract][Full Text] [Related]
14. [Clinico-genetic study of type I spinocerebelllar ataxia]. Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422 [TBL] [Abstract][Full Text] [Related]
15. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)]. Ishikawa K; Mizusawa H Nihon Rinsho; 1999 Apr; 57(4):880-5. PubMed ID: 10222783 [TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families. Sinke RJ; Ippel EF; Diepstraten CM; Beemer FA; Wokke JH; van Hilten BJ; Knoers NV; van Amstel HK; Kremer HP Arch Neurol; 2001 Nov; 58(11):1839-44. PubMed ID: 11708993 [TBL] [Abstract][Full Text] [Related]
17. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17. Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767 [TBL] [Abstract][Full Text] [Related]
18. Sisters homozygous for the spinocerebellar ataxia type 6 (SCA6)/CACNA1A gene associated with different clinical phenotypes. Kato T; Tanaka F; Yamamoto M; Yosida E; Indo T; Watanabe H; Yoshiwara T; Doyu M; Sobue G Clin Genet; 2000 Jul; 58(1):69-73. PubMed ID: 10945665 [TBL] [Abstract][Full Text] [Related]
19. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. Jodice C; Mantuano E; Veneziano L; Trettel F; Sabbadini G; Calandriello L; Francia A; Spadaro M; Pierelli F; Salvi F; Ophoff RA; Frants RR; Frontali M Hum Mol Genet; 1997 Oct; 6(11):1973-8. PubMed ID: 9302278 [TBL] [Abstract][Full Text] [Related]
20. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan. Hsieh M; Li SY; Tsai CJ; Chen YY; Liu CS; Chang CY; Ro LS; Chen DF; Chen SS; Li C Acta Neurol Scand; 1999 Sep; 100(3):189-94. PubMed ID: 10478584 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]