2288 related articles for article (PubMed ID: 15148151)
1. 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]
2. 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]
3. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
Sułek-Piatkowska A; Zdzienicka E; Raczyńska-Rakowicz M; Krysa W; Rajkiewicz M; Szirkowiec W; Zaremba J
Neurol Neurochir Pol; 2010; 44(3):238-45. PubMed ID: 20625959
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
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. Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
Wang J; Shen L; Lei L; Xu Q; Zhou J; Liu Y; Guan W; Pan Q; Xia K; Tang B; Jiang H
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):482-9. PubMed ID: 21743138
[TBL] [Abstract][Full Text] [Related]
8. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
Maruyama H; Izumi Y; Morino H; Oda M; Toji H; Nakamura S; Kawakami H
Am J Med Genet; 2002 Jul; 114(5):578-83. PubMed ID: 12116198
[TBL] [Abstract][Full Text] [Related]
9. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
[TBL] [Abstract][Full Text] [Related]
10. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
Juvonen V; Hietala M; Kairisto V; Savontaus ML
Acta Neurol Scand; 2005 Mar; 111(3):154-62. PubMed ID: 15691283
[TBL] [Abstract][Full Text] [Related]
11. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
Wang J; Xu Q; Lei L; Shen L; Jiang H; Li X; Zhou Y; Yi J; Zhou J; Yan X; Pan Q; Xia K; Tang B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):620-5. PubMed ID: 19953482
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
Kim JY; Park SS; Joo SI; Kim JM; Jeon BS
Mol Cells; 2001 Dec; 12(3):336-41. PubMed ID: 11804332
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Tang JG
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct; 31(5):702-5. PubMed ID: 17062934
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
[TBL] [Abstract][Full Text] [Related]
17. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
[TBL] [Abstract][Full Text] [Related]
18. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
Jiang H; Tang B; Xia K; Zhou Y; Xu B; Zhao G; Li H; Shen L; Pan Q; Cai F
J Neurol Sci; 2005 Sep; 236(1-2):25-9. PubMed ID: 15979648
[TBL] [Abstract][Full Text] [Related]
19. Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
Choubtum L; Witoonpanich P; Hanchaiphiboolkul S; Bhidayasiri R; Jitkritsadakul O; Pongpakdee S; Wetchaphanphesat S; Boonkongchuen P; Pulkes T
BMC Neurol; 2015 Sep; 15():166. PubMed ID: 26374734
[TBL] [Abstract][Full Text] [Related]
20. Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1-3, 6 and 7 CAG expansions.
Brusco A; Cagnoli C; Franco A; Dragone E; Nardacchione A; Grosso E; Mortara P; Mutani R; Migone N; Orsi L
J Neurol; 2002 Jul; 249(7):923-9. PubMed ID: 12140678
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
