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Results: 1 to 20 of 151

1.

Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6.

Wang PS, Chen HC, Wu HM, Lirng JF, Wu YT, Soong BW.

PLoS One. 2012;7(10):e47479. doi: 10.1371/journal.pone.0047479. Epub 2012 Oct 11.

PMID:
23094053
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Differences between spinocerebellar ataxias and multiple system atrophy-cerebellar type on proton magnetic resonance spectroscopy.

Lirng JF, Wang PS, Chen HC, Soong BW, Guo WY, Wu HM, Chang CY.

PLoS One. 2012;7(10):e47925. doi: 10.1371/journal.pone.0047925. Epub 2012 Oct 31.

PMID:
23118909
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Magnetic resonance spectroscopy of the cerebellum in patients with spinocerebellar ataxia type 3/Machado-Joseph disease.

Lei L, Liao Y, Liao W, Zhou J, Yuan Y, Wang J, Jiang H, Shen L, Tang B.

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jun;36(6):511-9. doi: 10.3969/j.issn.1672-7347.2011.06.007.

PMID:
21743142
[PubMed - indexed for MEDLINE]
Free Article
4.

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.

PMID:
10768629
[PubMed - indexed for MEDLINE]
5.

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.

Guerrini L, Lolli F, Ginestroni A, Belli G, Della Nave R, Tessa C, Foresti S, Cosottini M, Piacentini S, Salvi F, Plasmati R, De Grandis D, Siciliano G, Filla A, Mascalchi M.

Brain. 2004 Aug;127(Pt 8):1785-95. Epub 2004 Jul 7.

PMID:
15240431
[PubMed - indexed for MEDLINE]
Free Article
6.

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 23;71(13):982-9. doi: 10.1212/01.wnl.0000325057.33666.72. Epub 2008 Aug 6.

PMID:
18685131
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
9.

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

Schulz JB, Borkert J, Wolf S, Schmitz-Hübsch T, Rakowicz M, Mariotti C, Schöls L, Timmann D, van de Warrenburg B, Dürr A, Pandolfo M, Kang JS, Mandly AG, Nägele T, Grisoli M, Boguslawska R, Bauer P, Klockgether T, Hauser TK.

Neuroimage. 2010 Jan 1;49(1):158-68. doi: 10.1016/j.neuroimage.2009.07.027. Epub 2009 Jul 22. Erratum in: Neuroimage. 2010 May 1;50(4):1712. Schoels, Ludger [corrected to Schöls, Ludger].

PMID:
19631275
[PubMed - indexed for MEDLINE]
10.

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T.

Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Erratum in: Lancet Neurol. 2013 Jul;12(7):630.

PMID:
23707147
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
10942107
[PubMed - indexed for MEDLINE]
12.

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. Erratum in: Arch Neurol. 2003 Sep;60(9):1256.

PMID:
12810491
[PubMed - indexed for MEDLINE]
13.

Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging.

Boesch SM, Wolf C, Seppi K, Felber S, Wenning GK, Schocke M.

J Magn Reson Imaging. 2007 Mar;25(3):564-9.

PMID:
17326083
[PubMed - indexed for MEDLINE]
14.

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.

van de Warrenburg BP, Sinke RJ, Verschuuren-Bemelmans CC, Scheffer H, Brunt ER, Ippel PF, Maat-Kievit JA, Dooijes D, Notermans NC, Lindhout D, Knoers NV, Kremer HP.

Neurology. 2002 Mar 12;58(5):702-8.

PMID:
11889231
[PubMed - indexed for MEDLINE]
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. Chinese.

PMID:
9772474
[PubMed - indexed for MEDLINE]
16.

[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. Chinese.

PMID:
10514531
[PubMed - indexed for MEDLINE]
17.

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.

Jacobi H, Bauer P, Giunti P, Labrum R, Sweeney MG, Charles P, Dürr A, Marelli C, Globas C, Linnemann C, Schöls L, Rakowicz M, Rola R, Zdzienicka E, Schmitz-Hübsch T, Fancellu R, Mariotti C, Tomasello C, Baliko L, Melegh B, Filla A, Rinaldi C, van de Warrenburg BP, Verstappen CC, Szymanski S, Berciano J, Infante J, Timmann D, Boesch S, Hering S, Depondt C, Pandolfo M, Kang JS, Ratzka S, Schulz J, Tezenas du Montcel S, Klockgether T.

Neurology. 2011 Sep 13;77(11):1035-41. doi: 10.1212/WNL.0b013e31822e7ca0. Epub 2011 Aug 10.

PMID:
21832228
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.

Lin CH, Hwu WL, Chiang SC, Tai CH, Wu RM.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):434-8.

PMID:
17440947
[PubMed - indexed for MEDLINE]
19.

[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. doi: 10.3760/cma.j.issn.1003-9406.2009.06.005. Chinese.

PMID:
19953483
[PubMed - indexed for MEDLINE]
20.

Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6.

Boesch SM, Schocke M, Bürk K, Hollosi P, Fornai F, Aichner FT, Poewe W, Felber S.

J Magn Reson Imaging. 2001 Apr;13(4):553-9.

PMID:
11276099
[PubMed - indexed for MEDLINE]

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