290 related articles for article (PubMed ID: 11186889)
1. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia.
Storey E; du Sart D; Shaw JH; Lorentzos P; Kelly L; McKinley Gardner RJ; Forrest SM; Biros I; Nicholson GA
Am J Med Genet; 2000 Dec; 95(4):351-7. PubMed ID: 11186889
[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. 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]
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 five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.
Magaña JJ; Tapia-Guerrero YS; Velázquez-Pérez L; Cerecedo-Zapata CM; Maldonado-Rodríguez M; Jano-Ito JS; Leyva-García N; González-Piña R; Martínez-Cruz E; Hernández-Hernández O; Cisneros B
Clin Genet; 2014 Feb; 85(2):159-65. PubMed ID: 23368522
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.
Koutsis G; Pemble S; Sweeney MG; Paudel R; Wood NW; Panas M; Kladi A; Houlden H
J Neurol Sci; 2012 Jul; 318(1-2):178-80. PubMed ID: 22520093
[TBL] [Abstract][Full Text] [Related]
8. Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.
Jacobi H; du Montcel ST; Romanzetti S; Harmuth F; Mariotti C; Nanetti L; Rakowicz M; Makowicz G; Durr A; Monin ML; Filla A; Roca A; Schöls L; Hengel H; Infante J; Kang JS; Timmann D; Casali C; Masciullo M; Baliko L; Melegh B; Nachbauer W; Bürk-Gergs K; Schulz JB; Riess O; Reetz K; Klockgether T
Lancet Neurol; 2020 Sep; 19(9):738-747. PubMed ID: 32822634
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [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]
12. Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history?
Sura T; Eu-Ahsunthornwattana J; Youngcharoen S; Busabaratana M; Dejsuphong D; Trachoo O; Theerasasawat S; Tunteeratum A; Noparutchanodom C; Tunlayadechanont S
J Hum Genet; 2009 May; 54(5):284-8. PubMed ID: 19329990
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Jacobi H; du Montcel ST; Bauer P; Giunti P; Cook A; Labrum R; Parkinson MH; Durr A; Brice A; Charles P; Marelli C; Mariotti C; Nanetti L; Panzeri M; Rakowicz M; Sulek A; Sobanska A; Schmitz-Hübsch T; Schöls L; Hengel H; Baliko L; Melegh B; Filla A; Antenora A; Infante J; Berciano J; van de Warrenburg BP; Timmann D; Szymanski S; Boesch S; Kang JS; Pandolfo M; Schulz JB; Molho S; Diallo A; Klockgether T
Lancet Neurol; 2015 Nov; 14(11):1101-8. PubMed ID: 26377379
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
Schmitz-Hübsch T; Coudert M; Bauer P; Giunti P; Globas C; Baliko L; Filla A; Mariotti C; Rakowicz M; Charles P; Ribai P; Szymanski S; Infante J; van de Warrenburg BP; Dürr A; Timmann D; Boesch S; Fancellu R; Rola R; Depondt C; Schöls L; Zdienicka E; Kang JS; Döhlinger S; Kremer B; Stephenson DA; Melegh B; Pandolfo M; di Donato S; du Montcel ST; Klockgether T
Neurology; 2008 Sep; 71(13):982-9. PubMed ID: 18685131
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
Soong B W; Lu Y C; Choo K B; Lee H Y
Arch Neurol; 2001 Jul; 58(7):1105-9. PubMed ID: 11448300
[TBL] [Abstract][Full Text] [Related]
19. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].
Tan JQ; Wang P; Hu QP; Li SF; Shu W; Ma J; Fang L; Hua R; Ding Y; Yuan ZG
Yi Chuan; 2009 Jun; 31(6):605-10. PubMed ID: 19586860
[TBL] [Abstract][Full Text] [Related]
20. Adult onset spinocerebellar ataxia in a Canadian movement disorders clinic.
Kraft S; Furtado S; Ranawaya R; Parboosingh J; Bleoo S; McElligott K; Bridge P; Spacey S; Das S; Suchowersky O
Can J Neurol Sci; 2005 Nov; 32(4):450-8. PubMed ID: 16408574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
