193 related articles for article (PubMed ID: 9259274)
1. 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]
2. 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]
3. [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]
4. 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]
5. 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]
6. 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]
7. [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]
8. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
Ishikawa K; Tanaka H; Saito M; Ohkoshi N; Fujita T; Yoshizawa K; Ikeuchi T; Watanabe M; Hayashi A; Takiyama Y; Nishizawa M; Nakano I; Matsubayashi K; Miwa M; Shoji S; Kanazawa I; Tsuji S; Mizusawa H
Am J Hum Genet; 1997 Aug; 61(2):336-46. PubMed ID: 9311738
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls.
Shizuka M; Watanabe M; Ikeda Y; Mizushima K; Okamoto K; Shoji M
J Neurol Sci; 1998 Nov; 161(1):85-7. PubMed ID: 9879686
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
Yabe I; Sasaki H; Yamashita I; Takei A; Fukazawa T; Hamada T; Tashiro K
Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
Sasaki H; Kojima H; Yabe I; Tashiro K; Hamada T; Sawa H; Hiraga H; Nagashima K
Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
[TBL] [Abstract][Full Text] [Related]
16. CAG repeat expansions in patients with sporadic cerebellar ataxia.
Futamura N; Matsumura R; Fujimoto Y; Horikawa H; Suzumura A; Takayanagi T
Acta Neurol Scand; 1998 Jul; 98(1):55-9. PubMed ID: 9696528
[TBL] [Abstract][Full Text] [Related]
17. Clinical features and genetic analysis of a Spanish family with spinocerebellar ataxia 6.
Arpa J; Cuesta A; Cruz-Martínez A; Santiago S; Sarriá J; Palau F
Acta Neurol Scand; 1999 Jan; 99(1):43-7. PubMed ID: 9925237
[TBL] [Abstract][Full Text] [Related]
18. Gene dosage effect in spinocerebellar ataxia type 6 homozygotes: A clinical and neuropathological study.
Soga K; Ishikawa K; Furuya T; Iida T; Yamada T; Ando N; Ota K; Kanno-Okada H; Tanaka S; Shintaku M; Eishi Y; Mizusawa H; Yokota T
J Neurol Sci; 2017 Feb; 373():321-328. PubMed ID: 28131213
[TBL] [Abstract][Full Text] [Related]
19. Spinocerebellar ataxia type 6: MRI of three Japanese patients.
Satoh JI; Tokumoto H; Yukitake M; Matsui M; Matsuyama Z; Kawakami H; Nakamura S; Kuroda Y
Neuroradiology; 1998 Apr; 40(4):222-7. PubMed ID: 9592791
[TBL] [Abstract][Full Text] [Related]
20. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
Goldfarb LG; Vasconcelos O; Platonov FA; Lunkes A; Kipnis V; Kononova S; Chabrashvili T; Vladimirtsev VA; Alexeev VP; Gajdusek DC
Ann Neurol; 1996 Apr; 39(4):500-6. PubMed ID: 8619528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
