Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 225

1.

SCA2 may present as levodopa-responsive parkinsonism.

Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M.

Mov Disord. 2003 Apr;18(4):425-9.

PMID:
12671950
2.
3.

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?

Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A; French Parkinson's Disease Genetic Study Group..

Neurology. 2007 Nov 20;69(21):1970-5. Epub 2007 Jun 13.

PMID:
17568014
4.

The parkinsonian phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH.

Arch Neurol. 2004 Jan;61(1):35-8.

PMID:
14732617
5.

Complex phenotypes in an Indian family with homozygous SCA2 mutations.

Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB.

Ann Neurol. 2004 Jan;55(1):130-3.

PMID:
14705123
6.

Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease.

Infante J, Berciano J, Volpini V, Corral J, Polo JM, Pascual J, Combarros O.

Mov Disord. 2004 Jul;19(7):848-52.

PMID:
15254952
7.

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

Furtado S, Payami H, Lockhart PJ, Hanson M, Nutt JG, Singleton AA, Singleton A, Bower J, Utti RJ, Bird TD, de la Fuente-Fernandez R, Tsuboi Y, Klimek ML, Suchowersky O, Hardy J, Calne DB, Wszolek ZK, Farrer M, Gwinn-Hardy K, Stoessl AJ.

Mov Disord. 2004 Jun;19(6):622-9. Review.

PMID:
15197699
8.

Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.

Tan EK, Tong J, Pavanni R, Wong MC, Zhao Y.

Mov Disord. 2007 Oct 15;22(13):1971-4.

PMID:
17712857
9.

Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci.

Krygowska-Wajs A, Hussey JM, Hulihan M, Farrer MJ, Tsuboi Y, Uitti RJ, Wszolek ZK.

Parkinsonism Relat Disord. 2003 Mar;9(4):193-200.

PMID:
12618053
10.

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.

Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W, Adam A, Singleton A, Koroshetz W, Waters C, Hardy J, Farrer M.

Neurology. 2000 Sep 26;55(6):800-5.

PMID:
10993999
11.

Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.

Schraen-Maschke S, Brique S, Chartier-Harlin MC, Brique E, Destée A, Sablonnière B.

Am J Med Genet. 1999 Dec 15;88(6):738-41.

PMID:
10581499
12.

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
13.

CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.

Choudhry S, Mukerji M, Srivastava AK, Jain S, Brahmachari SK.

Hum Mol Genet. 2001 Oct 1;10(21):2437-46.

PMID:
11689490
14.

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.

Arch Neurol. 2004 Feb;61(2):209-12.

PMID:
14967767
15.

ATXN-2 CAG repeat expansions are interrupted in ALS patients.

Corrado L, Mazzini L, Oggioni GD, Luciano B, Godi M, Brusco A, D'Alfonso S.

Hum Genet. 2011 Oct;130(4):575-80. doi: 10.1007/s00439-011-1000-2. Epub 2011 May 3.

PMID:
21537950
16.

A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.

Markopoulou K, Wszolek ZK, Pfeiffer RF.

Ann Neurol. 1995 Sep;38(3):373-8.

PMID:
7668822
17.

Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.

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

Mov Disord. 2004 Nov;19(11):1357-60.

PMID:
15378681
18.

Brisk deep-tendon reflexes as a distinctive phenotype in an Argentinean spinocerebellar ataxia type 2 pedigree.

Rosa AL, Molina I, Kowaljow V, Conde CB.

Mov Disord. 2006 Jan;21(1):66-8.

PMID:
16108012
19.

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
20.

Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.

Wang C, Xu Y, Feng X, Ma J, Xie S, Zhang Y, Tang BS, Chan P.

Neurobiol Aging. 2015 Jan;36(1):545.e1-7. doi: 10.1016/j.neurobiolaging.2014.07.039. Epub 2014 Aug 2.

PMID:
25189117

Supplemental Content

Support Center