Burgunder JM - Search Results

1

High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.

Chen Q, Chen XP, Zou L, Zhou D, Gong QY, Burgunder JM, Shang HF. Chen Q, et al. Among authors: burgunder jm. Mov Disord. 2008 Apr 30;23(6):916-7. doi: 10.1002/mds.21980. Mov Disord. 2008. PMID: 18311828 No abstract available.

2

Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus.

Shang HF, Jiang XF, Burgunder JM, Chen Q, Zhou D. Shang HF, et al. Among authors: burgunder jm. Mov Disord. 2006 Dec;21(12):2217-20. doi: 10.1002/mds.21121. Mov Disord. 2006. PMID: 17013908

3

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

Zhang SS, Chen Q, Chen XP, Wang JG, Burgunder JM, Shang HF, Burgunder JM, Yang Y. Zhang SS, et al. Among authors: burgunder jm. Mov Disord. 2008 Apr 30;23(6):917-9. doi: 10.1002/mds.21942. Mov Disord. 2008. PMID: 18361476 No abstract available.

4

A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.

Chen XP, Zhang YW, Zhang SS, Chen Q, Burgunder JM, Wu SH, Yang Y, Luo ZM, Shang HF. Chen XP, et al. Among authors: burgunder jm. Mov Disord. 2008 Jul 30;23(10):1472-5. doi: 10.1002/mds.22008. Mov Disord. 2008. PMID: 18581468

5

Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum.

Chen Q, Lui S, Wang JG, Ou-Yang L, Zhou D, Burgunder JM, Gong QY, Shang HF. Chen Q, et al. Among authors: burgunder jm. Neurosci Lett. 2008 Aug 15;441(1):21-4. doi: 10.1016/j.neulet.2008.05.114. Epub 2008 Jun 7. Neurosci Lett. 2008. PMID: 18586399

6

Resting-state fMRI reveals potential neural correlates of impaired cognition in Huntington's disease.

Liu W, Yang J, Chen K, Luo C, Burgunder J, Gong Q, Shang H. Liu W, et al. Parkinsonism Relat Disord. 2016 Jun;27:41-6. doi: 10.1016/j.parkreldis.2016.04.017. Epub 2016 Apr 21. Parkinsonism Relat Disord. 2016. PMID: 27117563

7

Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.

Wei QQ, Chen Y, Zheng ZZ, Chen X, Huang R, Yang Y, Burgunder J, Shang HF. Wei QQ, et al. Parkinsonism Relat Disord. 2014 Aug;20(8):845-9. doi: 10.1016/j.parkreldis.2014.04.021. Epub 2014 May 2. Parkinsonism Relat Disord. 2014. PMID: 24824479

8

Diffusion imaging studies of Huntington's disease: A meta-analysis.

Liu W, Yang J, Burgunder J, Cheng B, Shang H. Liu W, et al. Parkinsonism Relat Disord. 2016 Nov;32:94-101. doi: 10.1016/j.parkreldis.2016.09.005. Epub 2016 Sep 7. Parkinsonism Relat Disord. 2016. PMID: 27624391 Review.

9

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF. Chen Y, et al. Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20. Neurobiol Aging. 2013. PMID: 23261770

10

Deep brain stimulation of the globus pallidus internal improves symptoms of chorea-acanthocytosis.

Li P, Huang R, Song W, Ji J, Burgunder JM, Wang X, Zhong Q, Kaelin-Lang A, Wang W, Shang HF. Li P, et al. Among authors: burgunder jm. Neurol Sci. 2012 Apr;33(2):269-74. doi: 10.1007/s10072-011-0741-y. Epub 2011 Aug 24. Neurol Sci. 2012. PMID: 21863267 Free article.

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