He S - Search Results

1

Characterization of Age-dependent Behavior Deficits in the PGC-1α Knockout Mouse, in Relevance to the Parkinson's Disease Model.

Sun Z, Ma X, Yang H, Chen S, He S, Sun R, Lu H, Zhang J. Sun Z, et al. Among authors: he s. Neuroscience. 2020 Aug 1;440:39-47. doi: 10.1016/j.neuroscience.2020.05.015. Epub 2020 May 19. Neuroscience. 2020. PMID: 32439544

2

[Survey of dentomaxillary deformities in 1032 middle school students].

He SH, Chen SS. He SH, et al. Shanghai Kou Qiang Yi Xue. 1994 Jun;3(2):74-5. Shanghai Kou Qiang Yi Xue. 1994. PMID: 15160144 Chinese. No abstract available.

3

Crossed cerebellar diaschisis detected by arterial spin-labeled perfusion magnetic resonance imaging in subacute ischemic stroke.

Chen S, Guan M, Lian HJ, Ma LJ, Shang JK, He S, Ma MM, Zhang ML, Li ZY, Wang MY, Shi DP, Zhang JW. Chen S, et al. Among authors: he s. J Stroke Cerebrovasc Dis. 2014 Oct;23(9):2378-83. doi: 10.1016/j.jstrokecerebrovasdis.2014.05.009. Epub 2014 Aug 31. J Stroke Cerebrovasc Dis. 2014. PMID: 25183560

4

Reduced cerebral blood flow in genetic prion disease with PRNP D178N-129M mutation: an arterial spin labeling MRI study.

Chen S, Guan M, Shang JK, He S, Zhang ML, Ma MM, Zhang JW. Chen S, et al. Among authors: he s. J Clin Neurosci. 2015 Jan;22(1):204-6. doi: 10.1016/j.jocn.2014.05.040. Epub 2014 Sep 11. J Clin Neurosci. 2015. PMID: 25220284

5

Postencephalitic parkinsonism and selective involvement of substantia nigra.

He S, Yuan LP, Zhang JW, Han X. He S, et al. Neurol Sci. 2015 Apr;36(4):653-5. doi: 10.1007/s10072-015-2064-x. Epub 2015 Jan 11. Neurol Sci. 2015. PMID: 25577509 No abstract available.

6

Probable novel PSEN2 Pro123Leu mutation in a Chinese Han family of Alzheimer's disease.

Xia M, Chen S, Shi Y, Huang Y, Xu J, Zhao T, He S, Wu Y, Xu C, Zang W, Zhang J. Xia M, et al. Among authors: he s. Neurobiol Aging. 2015 Dec;36(12):3334.e13-3334.e18. doi: 10.1016/j.neurobiolaging.2015.09.003. Epub 2015 Sep 8. Neurobiol Aging. 2015. PMID: 26422362

7

Serum uric acid and lipid profiles in sporadic Creutzfeldt-Jakob disease.

Chen S, He S, Shang JK, Ma MM, Xu CS, Shi XH, Zhang JW. Chen S, et al. Among authors: he s. Clin Biochem. 2016 Feb;49(3):292-4. doi: 10.1016/j.clinbiochem.2015.09.017. Epub 2015 Oct 8. Clin Biochem. 2016. PMID: 26454226

8

Vertebrobasilar artery fenestration with moyamoya disease.

He S, Wu YY, Zhao T, Chen S, Zhang JW. He S, et al. Neurol Sci. 2016 Feb;37(2):301-3. doi: 10.1007/s10072-015-2402-z. Epub 2015 Oct 24. Neurol Sci. 2016. PMID: 26498288 No abstract available.

9

[The study of clinical characteristics and molecular genetics in a large spinocerebellar ataxia3 pedigree].

Huang Y, Xia M, Ren X, He S, Zhang J. Huang Y, et al. Among authors: he s. Zhonghua Yi Xue Za Zhi. 2015 Jul 7;95(25):1990-3. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26710806 Chinese.

10

The clinical features in Chinese patients with PRNP D178N mutation.

Chen S, He S, Shi XH, Shen XJ, Liang KK, Zhao JH, Yan BC, Zhang JW. Chen S, et al. Among authors: he s. Acta Neurol Scand. 2018 Aug;138(2):151-155. doi: 10.1111/ane.12924. Epub 2018 Mar 22. Acta Neurol Scand. 2018. PMID: 29569252

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