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Items: 1 to 20 of 110

1.

Spinocerebellar ataxia type 2: progression before diagnosis.

Klockgether T.

Lancet Neurol. 2014 May;13(5):445-6. doi: 10.1016/S1474-4422(14)70044-4. Epub 2014 Mar 20. No abstract available.

PMID:
24657152
2.

[Spinocerebellar ataxia type 8(SCA 8)].

Izumi Y, Maruyama H, Kawakami H.

No To Shinkei. 2001 Jan;53(1):34-40. Review. Japanese. No abstract available.

PMID:
11211728
3.

Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.

Gupta SN, Marks HG.

J Neurol Sci. 2008 Jan 15;264(1-2):173-6. Epub 2007 Aug 27.

PMID:
17720198
4.

Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.

Velázquez-Pérez L, Rodríguez-Labrada R, Canales-Ochoa N, Montero JM, Sánchez-Cruz G, Aguilera-Rodríguez R, Almaguer-Mederos LE, Laffita-Mesa JM.

Lancet Neurol. 2014 May;13(5):482-9. doi: 10.1016/S1474-4422(14)70027-4. Epub 2014 Mar 20.

PMID:
24657153
5.

Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism.

Shan DE, Soong BW, Sun CM, Lee SJ, Liao KK, Liu RS.

Ann Neurol. 2001 Dec;50(6):812-5.

PMID:
11761482
6.

Machado-Joseph disease and other rare spinocerebellar ataxias.

Matilla-Dueñas A.

Adv Exp Med Biol. 2012;724:172-88. doi: 10.1007/978-1-4614-0653-2_14. Review.

PMID:
22411243
7.

Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.

Horton LC, Frosch MP, Vangel MG, Weigel-DiFranco C, Berson EL, Schmahmann JD.

Cerebellum. 2013 Apr;12(2):176-93. doi: 10.1007/s12311-012-0412-4.

8.

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.

PMID:
15080863
9.

Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats.

Ansorge O, Giunti P, Michalik A, Van Broeckhoven C, Harding B, Wood N, Scaravilli F.

Ann Neurol. 2004 Sep;56(3):448-52.

PMID:
15349877
10.

[Typical anticipation in type 7 spinocerebellar ataxia].

Jäger M, von Rosen F, Fesl G, Gasser T.

Nervenarzt. 2000 Oct;71(10):835-8. German.

PMID:
11082815
11.

Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.

Netravathi M, Pal PK, Purushottam M, Thennarasu K, Mukherjee M, Jain S.

J Neurol Sci. 2009 Feb 15;277(1-2):83-6. doi: 10.1016/j.jns.2008.10.016. Epub 2008 Dec 2.

PMID:
19049837
12.

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 15;236(1-2):25-9.

PMID:
15979648
13.

Sporadic SCA8 mutation resembling corticobasal degeneration.

Baba Y, Uitti RJ, Farrer MJ, Wszolek ZK.

Parkinsonism Relat Disord. 2005 May;11(3):147-50.

PMID:
15823478
14.

[Report of a family with spinocerebellar ataxia and SCA1 gene mutation].

Chen J, Wang Y, Zeng G, Li G.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):138-9. doi: 10.3760/cma.j.issn.1003-9406.2015.01.035. Chinese. No abstract available.

PMID:
25636116
15.

Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.

Zhou YX, Qiao WH, Gu WH, Xie H, Tang BS, Zhou LS, Yang BX, Takiyama Y, Tsuji S, He HY, Deng CX, Goldfarb LG, Wang GX.

Arch Neurol. 2001 May;58(5):789-94.

PMID:
11346374
16.

Spinocerebellar ataxia type 2 in a Turkish family.

Dirik E, Yiş U, Başak N, Soydan E, Hüdaoğlu O, Ozgönül F.

J Child Neurol. 2007 Jul;22(7):891-4.

PMID:
17715286
17.

[Study of a family from Yunnan with five generations and eight individuals affected with spinocerebellar ataxia].

Zhang L, Yang D, Li H, Zhu Y, Liang L, Chen T.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):141-3. doi: 10.3760/cma.j.issn.1003-9406.2015.01.037. Chinese. No abstract available.

PMID:
25636118
18.

Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10.

Alonso I, Jardim LB, Artigalas O, Saraiva-Pereira ML, Matsuura T, Ashizawa T, Sequeiros J, Silveira I.

Neurology. 2006 May 23;66(10):1602-4. No abstract available.

PMID:
16717236
19.

Recent advances in hereditary spinocerebellar ataxias.

van de Warrenburg BP, Sinke RJ, Kremer B.

J Neuropathol Exp Neurol. 2005 Mar;64(3):171-80. Review.

20.

[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. Chinese.

PMID:
17650485
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