Similar articles for PMID: 22054283

Year	Number of Results
1999	2
2000	1
2001	1
2002	4
2003	4
2004	5
2005	5
2006	6
2007	5
2008	7
2009	11
2010	7
2011	7
2012	10
2013	7
2014	7
2015	5
2016	7
2017	6
2018	2
2019	3
2020	2
2021	4
2022	2
2024	0

1

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

Chen Y, Burgunder JM, Song W, Huang R, Shang HF. Chen Y, et al. Eur J Neurol. 2012 Jun;19(6):924-6. doi: 10.1111/j.1468-1331.2011.03582.x. Epub 2011 Nov 7. Eur J Neurol. 2012. PMID: 22054283

2

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. Caputo M, et al. J Neurogenet. 2013 Jun;27(1-2):16-8. doi: 10.3109/01677063.2012.761697. Epub 2013 Feb 13. J Neurogenet. 2013. PMID: 23405979

3

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. Sharma N, et al. Mov Disord. 2010 Oct 15;25(13):2183-7. doi: 10.1002/mds.23225. Mov Disord. 2010. PMID: 20669276 Free PMC article.

4

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. Chen Y, et al. J Neurol Sci. 2012 Dec 15;323(1-2):228-31. doi: 10.1016/j.jns.2012.09.025. Epub 2012 Oct 9. J Neurol Sci. 2012. PMID: 23058565

5

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. Kamm C, et al. Neurology. 2008 Jun 3;70(23):2261-2. doi: 10.1212/01.wnl.0000313838.05734.8a. Neurology. 2008. PMID: 18519876 No abstract available.

6

Phenotype of the DYT1 mutation in the TOR1A gene in a Polish population of patients with dystonia. A preliminary report.

Gajos A, Piaskowski S, Sławek J, Ochudło S, Opala G, Łobińska A, Honczarenko K, Budrewicz S, Koszewicz M, Pełszyńska B, Liberski PP, Bogucki A. Gajos A, et al. Neurol Neurochir Pol. 2007 Nov-Dec;41(6):487-94. Neurol Neurochir Pol. 2007. PMID: 18224570

7

Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp.

Ritz K, Groen JL, Kruisdijk JJ, Baas F, Koelman JH, Tijssen MA. Ritz K, et al. Mov Disord. 2009 Jul 15;24(9):1390-2. doi: 10.1002/mds.22632. Mov Disord. 2009. PMID: 19441135

8

The p.Asp216His TOR1A allele effect is not found in the French population.

Frédéric MY, Clot F, Blanchard A, Dhaenens CM, Lesca G, Cif L, Dürr A, Vidailhet M, Sablonniere B, Calender A, Martinez M, Molinari N, Brice A, Claustres M, Tuffery-Giraud S, Collod-Beroud G. Frédéric MY, et al. Mov Disord. 2009 Apr 30;24(6):919-21. doi: 10.1002/mds.22407. Mov Disord. 2009. PMID: 19260107 Free article.

9

The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?

Brüggemann N, Kock N, Lohmann K, König IR, Rakovic A, Hagenah J, Schmidt A, Ziegler A, Jabusch HC, Siebner H, Altenmüller E, Münchau A, Klein C. Brüggemann N, et al. Neurology. 2009 Apr 21;72(16):1441-3. doi: 10.1212/WNL.0b013e3181a1861e. Neurology. 2009. PMID: 19380705 No abstract available.

10

Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population.

Wang L, Duan C, Gao Y, Xu W, Ding J, Liu VT, Wu Y. Wang L, et al. Clin Neurol Neurosurg. 2016 Mar;142:26-30. doi: 10.1016/j.clineuro.2016.01.018. Epub 2016 Jan 12. Clin Neurol Neurosurg. 2016. PMID: 26803725

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