Burgunder JM - Search Results

1

Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China.

Mao XY, Burgunder JM, Zhang ZJ, An XK, Zhang JH, Yang Y, Li T, Wang YC, Chang XL, Peng R. Mao XY, et al. Among authors: burgunder jm. Neurosci Lett. 2010 Jan 22;469(2):256-9. doi: 10.1016/j.neulet.2009.12.007. Epub 2009 Dec 11. Neurosci Lett. 2010. PMID: 20004703

2

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

An XK, Peng R, Li T, Burgunder JM, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Zhang ZJ. An XK, et al. Among authors: burgunder jm. Eur J Neurol. 2008 Mar;15(3):301-5. doi: 10.1111/j.1468-1331.2007.02052.x. Epub 2008 Jan 14. Eur J Neurol. 2008. PMID: 18201193

3

Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese population.

Zhang ZJ, Burgunder JM, An XK, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Mao XY, Peng R. Zhang ZJ, et al. Among authors: burgunder jm. Neurosci Lett. 2008 Sep 19;442(3):200-2. doi: 10.1016/j.neulet.2008.07.012. Epub 2008 Jul 10. Neurosci Lett. 2008. PMID: 18638528

4

ATP13A2 G2236A variant is rare in patients with early-onset Parkinson's disease and familial Parkinson's disease from Mainland China.

Mao XY, Burgunder JM, Zhang ZJ, Chang XL, Peng R, Burgunder JM, Yang Y, Wang YC, Li T, Zhang ZJ. Mao XY, et al. Among authors: burgunder jm. Parkinsonism Relat Disord. 2010 Mar;16(3):235-6. doi: 10.1016/j.parkreldis.2009.11.010. Epub 2009 Dec 24. Parkinsonism Relat Disord. 2010. PMID: 20036179 No abstract available.

5

Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China.

Zhang SS, Fang DF, Hu XH, Burgunder JM, Chen XP, Zhang YW, Shang HF. Zhang SS, et al. Among authors: burgunder jm. Eur J Neurol. 2010 Jun 1;17(6):846-51. doi: 10.1111/j.1468-1331.2009.02944.x. Epub 2010 Jan 26. Eur J Neurol. 2010. PMID: 20113340

6

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. Among authors: burgunder jm. 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

7

PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China.

Chen YP, Song W, Yang J, Zheng ZZ, Huang R, Chen K, Zhao B, Chen XP, Burgunder JM, Shang HF. Chen YP, et al. Among authors: burgunder jm. Eur J Neurol. 2014;21(1):174-6. doi: 10.1111/ene.12122. Epub 2013 Mar 16. Eur J Neurol. 2014. PMID: 23496026

8

Screening of GABA(A)-receptor gene mutations in primary dystonia.

Shang H, Lang D, Burgunder JM, Kaelin-Lang A. Shang H, et al. Among authors: burgunder jm. Eur J Neurol. 2007 Oct;14(10):1179-81. doi: 10.1111/j.1468-1331.2007.01910.x. Eur J Neurol. 2007. PMID: 17880575

9

Expression of neurotransmitter genes in motor regions of the dyskinetic rat after iminodipropionitrile.

Fritschi JA, Lauterburg T, Burgunder JM. Fritschi JA, et al. Among authors: burgunder jm. Neurosci Lett. 2003 Aug 14;347(1):45-8. doi: 10.1016/s0304-3940(03)00616-5. Neurosci Lett. 2003. PMID: 12865138

10

Clinical and molecular genetic evaluation of patients with primary dystonia.

Shang H, Clerc N, Lang D, Kaelin-Lang A, Burgunder JM. Shang H, et al. Among authors: burgunder jm. Eur J Neurol. 2005 Feb;12(2):131-8. doi: 10.1111/j.1468-1331.2004.00974.x. Eur J Neurol. 2005. PMID: 15679701

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