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Results: 1 to 20 of 125

Similar articles for PubMed (Select 23107556)

1.

TOR1A sequence variants and the association with early-onset primary dystonia in the Chinese Han population.

Cheng FB, Wan XH, Zhang Y, Miao J, Sun Y, Sun YB, Feng JC.

Parkinsonism Relat Disord. 2013 Mar;19(3):399-401. doi: 10.1016/j.parkreldis.2012.08.013. Epub 2012 Oct 26. No abstract available.

PMID:
23107556
2.

Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population.

Chen Y, Chen K, Burgunder JM, Song W, Huang R, Zhao B, Cao B, Chen X, Jiang Y, Shang HF.

J Neurol Sci. 2012 Dec 15;323(1-2):228-31. doi: 10.1016/j.jns.2012.09.025. Epub 2012 Oct 9.

PMID:
23058565
3.

Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort.

Chen Y, Burgunder JM, Song W, Huang R, Shang HF.

Eur J Neurol. 2012 Jun;19(6):924-6. doi: 10.1111/j.1468-1331.2011.03582.x. Epub 2011 Nov 7.

PMID:
22054283
4.

Analysis of D216H polymorphism in Argentinean patients with primary dystonia.

Caputo M, Irisarri M, Perandones C, Alechine E, Pellene LA, Roca CU, Micheli FE, Corach D.

J Neurogenet. 2013 Jun;27(1-2):16-8. doi: 10.3109/01677063.2012.761697. Epub 2013 Feb 13.

PMID:
23405979
5.

The GAG deletion in Tor1A (DYT1) is a rare cause of complex musician's dystonia.

Schmidt A, Altenmüller E, Jabusch HC, Lee A, Wiegers K, Klein C, Lohmann K.

Parkinsonism Relat Disord. 2012 Jun;18(5):690-1. doi: 10.1016/j.parkreldis.2011.12.008. Epub 2012 Jan 4. No abstract available.

PMID:
22226333
6.

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

Groen JL, Ritz K, Tanck MW, van de Warrenburg BP, van Hilten JJ, Aramideh M, Baas F, Tijssen MA.

Mov Disord. 2013 Jun;28(6):827-31. doi: 10.1002/mds.25381. Epub 2013 Mar 4.

PMID:
23460578
7.

Genotype-phenotype interactions in primary dystonias revealed by differential changes in brain structure.

Draganski B, Schneider SA, Fiorio M, Klöppel S, Gambarin M, Tinazzi M, Ashburner J, Bhatia KP, Frackowiak RS.

Neuroimage. 2009 Oct 1;47(4):1141-7. doi: 10.1016/j.neuroimage.2009.03.057. Epub 2009 Apr 1.

8.

Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism.

Kamm C, Fischer H, Garavaglia B, Kullmann S, Sharma M, Schrader C, Grundmann K, Klein C, Borggraefe I, Lobsien E, Kupsch A, Nardocci N, Gasser T.

Neurology. 2008 Jun 3;70(23):2261-2. doi: 10.1212/01.wnl.0000313838.05734.8a. No abstract available.

PMID:
18519876
9.

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Sharma N, Franco RA Jr, Kuster JK, Mitchell AA, Fuchs T, Saunders-Pullman R, Raymond D, Brin MF, Blitzer A, Bressman SB, Ozelius LJ.

Mov Disord. 2010 Oct 15;25(13):2183-7. doi: 10.1002/mds.23225.

10.

DYT1 mutations in early onset primary torsion dystonia and Parkinson disease patients in Chinese populations.

Yang JF, Wu T, Li JY, Li YJ, Zhang YL, Chan P.

Neurosci Lett. 2009 Jan 30;450(2):117-21. doi: 10.1016/j.neulet.2008.10.111. Epub 2008 Nov 20.

PMID:
19038309
11.

Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.

Kamm C, Asmus F, Mueller J, Mayer P, Sharma M, Muller UJ, Beckert S, Ehling R, Illig T, Wichmann HE, Poewe W, Mueller JC, Gasser T.

Neurology. 2006 Nov 28;67(10):1857-9.

PMID:
17130424
12.

Clinical and genetic evaluation of DYT1 and DYT6 primary dystonia in China.

Cheng FB, Wan XH, Feng JC, Wang L, Yang YM, Cui LY.

Eur J Neurol. 2011 Mar;18(3):497-503. doi: 10.1111/j.1468-1331.2010.03192.x. Epub 2010 Sep 6.

PMID:
20825472
13.

Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.

Akbari MT, Zand Z, Shahidi GA, Hamid M.

Med Princ Pract. 2012;21(5):462-6. doi: 10.1159/000336783. Epub 2012 Apr 6.

PMID:
22487959
14.

Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.

Saunders-Pullman R, Fuchs T, San Luciano M, Raymond D, Brashear A, Ortega R, Deik A, Ozelius LJ, Bressman SB.

Mov Disord. 2014 May;29(6):812-8. doi: 10.1002/mds.25818. Epub 2014 Feb 5.

15.

Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.

Cheng FB, Feng JC, Ma LY, Miao J, Ott T, Wan XH, Grundmann K.

Mov Disord. 2014 Jul;29(8):1079-83. doi: 10.1002/mds.25921. Epub 2014 May 23.

PMID:
24862462
16.

High-throughput mutational analysis of TOR1A in primary dystonia.

Xiao J, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Blitzer A, Batish SD, Wszolek ZK, Uitti RJ, Hedera P, Simon DK, Tarsy D, Truong DD, Frei KP, Pfeiffer RF, Gong S, Zhao Y, LeDoux MS.

BMC Med Genet. 2009 Mar 11;10:24. doi: 10.1186/1471-2350-10-24.

17.

Association study of the single nucleotide polymorphisms of PARK2 and PACRG with leprosy susceptibility in Chinese population.

Li J, Liu H, Liu J, Fu X, Yu Y, Yu G, Chen S, Chu T, Lu N, Bao F, Yuan C, Zhang F.

Eur J Hum Genet. 2012 May;20(5):488-9. doi: 10.1038/ejhg.2011.190. Epub 2011 Oct 19. No abstract available.

18.

Genetic study of two single nucleotide polymorphisms within corresponding microRNAs and susceptibility to tuberculosis in a Chinese Tibetan and Han population.

Li D, Wang T, Song X, Qucuo M, Yang B, Zhang J, Wang J, Ying B, Tao C, Wang L.

Hum Immunol. 2011 Jul;72(7):598-602. doi: 10.1016/j.humimm.2011.03.004. Epub 2011 Apr 12. Erratum in: Hum Immunol. 2012 Jan;73(1):140. Li, Dingdong [corrected to Li, Dongdong].

PMID:
21524676
19.

No association between the Nuclear Receptor Coactivator 7 gene and schizophrenia in the Chinese Han population.

Liu Y, Shi Y, Guo T, Gao J, Qin W, Li S, Tang W, Feng G, Zhu S, Liu H, He L.

Schizophr Res. 2007 Jan;89(1-3):360-1. Epub 2006 Oct 31. No abstract available.

PMID:
17079118
20.

Lack of association between the BDNF C270T polymorphism and schizophrenia in a Chinese Han population.

Li W, Wei J, Zhou DF, Tan YL, Cao YL, Zhang XY, Wu G, Kosten TA, Kosten TR.

Schizophr Res. 2007 Dec;97(1-3):297-8. Epub 2007 Jul 31. No abstract available.

PMID:
17669628
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