445 related articles for article (PubMed ID: 19953483)
1. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
Tang B; Wang D; Xia J
Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
[TBL] [Abstract][Full Text] [Related]
7. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. 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]
14. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
Schöls L; Amoiridis G; Büttner T; Przuntek H; Epplen JT; Riess O
Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486
[TBL] [Abstract][Full Text] [Related]
15. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
Xie QY; Liang XL; Li XH; Feng YQ
Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
[TBL] [Abstract][Full Text] [Related]
16. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
Basu P; Chattopadhyay B; Gangopadhaya PK; Mukherjee SC; Sinha KK; Das SK; Roychoudhury S; Majumder PP; Bhattacharyya NP
Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
[TBL] [Abstract][Full Text] [Related]
17. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
Silveira I; Coutinho P; Maciel P; Gaspar C; Hayes S; Dias A; Guimarães J; Loureiro L; Sequeiros J; Rouleau GA
Am J Med Genet; 1998 Mar; 81(2):134-8. PubMed ID: 9613852
[TBL] [Abstract][Full Text] [Related]
18. Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7.
Mao R; Aylsworth AS; Potter N; Wilson WG; Breningstall G; Wick MJ; Babovic-Vuksanovic D; Nance M; Patterson MC; Gomez CM; Snow K
Am J Med Genet; 2002 Jul; 110(4):338-45. PubMed ID: 12116207
[TBL] [Abstract][Full Text] [Related]
19. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
Pujana MA; Volpini V; Gratacós M; Corral J; Banchs I; Sánchez A; Genís D; Cervera C; Estivill X
J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
[TBL] [Abstract][Full Text] [Related]
20. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
García-Planells J; Cuesta A; Vilchez JJ; Martínez F; Prieto F; Palau F
J Med Genet; 1999 Feb; 36(2):148-51. PubMed ID: 10051016
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
