235 related articles for article (PubMed ID: 35469073)
1. Spinocerebellar ataxia in a cohort of patients from Rio de Janeiro.
Alvarenga MP; Siciliani LC; Carvalho RS; Ganimi MC; Penna PS
Neurol Sci; 2022 Aug; 43(8):4997-5005. PubMed ID: 35469073
[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. 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]
4. 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]
5. 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]
6. Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.
Atadzhanov M; Smith DC; Mwaba MH; Siddiqi OK; Bryer A; Greenberg LJ
Cerebellum Ataxias; 2017; 4():17. PubMed ID: 29214039
[TBL] [Abstract][Full Text] [Related]
7. The wide spectrum of spinocerebellar ataxias (SCAs).
Manto MU
Cerebellum; 2005; 4(1):2-6. PubMed ID: 15895552
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
Jiang H; Tang BS; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
Chin Med J (Engl); 2005 May; 118(10):837-43. PubMed ID: 15989765
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Central auditory processing in patients with spinocerebellar ataxia.
Zeigelboim BS; de Carvalho HA; Teive HA; Liberalesso PB; Jurkiewicz AL; da Silva Abdulmassih EM; Marques JM; Cordeiro ML
Hear Res; 2015 Sep; 327():235-44. PubMed ID: 26183435
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
Rakowicz M; Zdzienicka E; Poniatowska R; Waliniowska E; Sułek A; Jakubowska T; Niedzielska K; Rola R; Wierzbicka A; Hoffman-Zacharska D; Głazowski C; Jakubczyk T; Niewiadomska M; Zaremba J
Neurol Neurochir Pol; 2005; 39(4):263-275. PubMed ID: 16096942
[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. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
Rüb U; Brunt ER; Petrasch-Parwez E; Schöls L; Theegarten D; Auburger G; Seidel K; Schultz C; Gierga K; Paulson H; van Broeckhoven C; Deller T; de Vos RA
Neuropathol Appl Neurobiol; 2006 Dec; 32(6):635-49. PubMed ID: 17083478
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. [Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].
Jiang H; Tang B; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):1-4. PubMed ID: 15696468
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
