199 related articles for article (PubMed ID: 10548917)
1. [Hereditary ataxias in Akita prefecture].
Sugawara M; Toyoshima I; Kato K; Wada C; Imota T; Hirota K; Ishiguro H; Kagaya H; Hirata A; Ogasawara M; Masamune O
Rinsho Shinkeigaku; 1999 Jul; 39(7):763-6. PubMed ID: 10548917
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of spinocerebellar degenerations in the Hokuriku district in Japan.
Shibata-Hamaguchi A; Ishida C; Iwasa K; Yamada M
Neuroepidemiology; 2009; 32(3):176-83. PubMed ID: 19169038
[TBL] [Abstract][Full Text] [Related]
3. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan.
Mizushima K; Shibata Y; Shirai S; Matsushima M; Miyatake S; Iwata I; Yaguchi H; Matsumoto N; Yabe I
J Hum Genet; 2024 Jan; 69(1):27-31. PubMed ID: 37848721
[TBL] [Abstract][Full Text] [Related]
6. Molecular genetics of hereditary ataxias.
Banfi S; Zoghbi HY
Baillieres Clin Neurol; 1994 Aug; 3(2):281-95. PubMed ID: 7952848
[TBL] [Abstract][Full Text] [Related]
7. Fluorescent multiplex PCR--fast method for autosomal dominant spinocerebellar ataxias screening.
Bauer PO; Kotliarova SE; Matoska V; Musova Z; Hedvicakova P; Boday A; Tomek A; Nukina N; Goetz P
Genetika; 2005 Jun; 41(6):830-7. PubMed ID: 16080609
[TBL] [Abstract][Full Text] [Related]
8. [Autosomal dominant spinocerebellar ataxia].
Legros B; Manto MU
Rev Med Brux; 1999 Dec; 20(6):495-503. PubMed ID: 10672773
[TBL] [Abstract][Full Text] [Related]
9. [Frequencies of triplet repeat disorders in dominantly inherited spinocerebellar ataxia (SCA) in the Japanese].
Sasaki H; Tashiro K
Nihon Rinsho; 1999 Apr; 57(4):787-91. PubMed ID: 10222766
[TBL] [Abstract][Full Text] [Related]
10. Multiplex families with multiple system atrophy.
Hara K; Momose Y; Tokiguchi S; Shimohata M; Terajima K; Onodera O; Kakita A; Yamada M; Takahashi H; Hirasawa M; Mizuno Y; Ogata K; Goto J; Kanazawa I; Nishizawa M; Tsuji S
Arch Neurol; 2007 Apr; 64(4):545-51. PubMed ID: 17420317
[TBL] [Abstract][Full Text] [Related]
11. [Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory].
van de Warrenburg BP
Ned Tijdschr Geneeskd; 2001 May; 145(20):962-7. PubMed ID: 11396263
[TBL] [Abstract][Full Text] [Related]
12. Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.
Cagnoli C; Stevanin G; Michielotto C; Gerbino Promis G; Brussino A; Pappi P; Durr A; Dragone E; Viemont M; Gellera C; Brice A; Migone N; Brusco A
J Mol Diagn; 2006 Feb; 8(1):128-32. PubMed ID: 16436644
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
Xie QY; Liang XL; Li XH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):71-3. PubMed ID: 15696485
[TBL] [Abstract][Full Text] [Related]
15. [Spinocerebellar degeneration in Japan--the feature from an epidemiological study].
Kita K
Rinsho Shinkeigaku; 1993 Dec; 33(12):1279-84. PubMed ID: 8174325
[TBL] [Abstract][Full Text] [Related]
16. [Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations].
Tsuji S
Rinsho Shinkeigaku; 2004 Nov; 44(11):785-7. PubMed ID: 15651291
[TBL] [Abstract][Full Text] [Related]
17. [Differential diagnosis of spinocerebellar ataxia].
Sasaki H
Rinsho Shinkeigaku; 2002 Nov; 42(11):1069-72. PubMed ID: 12784668
[TBL] [Abstract][Full Text] [Related]
18. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
Lee WY; Jin DK; Oh MR; Lee JE; Song SM; Lee EA; Kim GM; Chung JS; Lee KH
Arch Neurol; 2003 Jun; 60(6):858-63. PubMed ID: 12810491
[TBL] [Abstract][Full Text] [Related]
19. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin.
Velázquez Pérez L; Cruz GS; Santos Falcón N; Enrique Almaguer Mederos L; Escalona Batallan K; Rodríguez Labrada R; Paneque Herrera M; Laffita Mesa JM; Rodríguez Díaz JC; Rodríguez RA; González Zaldivar Y; Coello Almarales D; Almaguer Gotay D; Jorge Cedeño H
Neurosci Lett; 2009 Apr; 454(2):157-60. PubMed ID: 19429075
[TBL] [Abstract][Full Text] [Related]
20. The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).
Matsuyama Z; Izumi Y; Kameyama M; Kawakami H; Nakamura S
J Med Genet; 1999 Jul; 36(7):546-8. PubMed ID: 10424816
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
