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  • Showing results for sheng di chen. Search instead for Sheng-Qi Chen (1 item)

Corrigendum: Detection of Microbial 16S rRNA Gene in the Blood of Patients With Parkinson's Disease.

Qian Y, Yang X, Xu S, Wu C, Qin N, Chen SD, Xiao Q.

Front Aging Neurosci. 2019 Jan 30;11:4. doi: 10.3389/fnagi.2019.00004. eCollection 2019.


Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.

Tian WT, Luan XH, Zhou HY, Zhang C, Huang XJ, Liu XL, Chen SD, Tang HD, Cao L.

Neuromuscul Disord. 2019 Jan 6. pii: S0960-8966(18)31011-3. doi: 10.1016/j.nmd.2019.01.001. [Epub ahead of print]


Computerized cognitive training for Chinese mild cognitive impairment patients: A neuropsychological and fMRI study.

Li BY, He NY, Qiao Y, Xu HM, Lu YZ, Cui PJ, Ling HW, Yan FH, Tang HD, Chen SD.

Neuroimage Clin. 2019 Jan 26;22:101691. doi: 10.1016/j.nicl.2019.101691. [Epub ahead of print]


TRPC6 mRNA levels in peripheral leucocytes of patients with Alzheimer's disease and mild cognitive impairment: A case-control study.

Chen JM, Li QW, Liu JS, Jiang GX, Liu JR, Chen SD, Cheng Q.

Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jan 23;92:279-284. doi: 10.1016/j.pnpbp.2019.01.009. [Epub ahead of print]


Management Recommendations on Sleep Disturbance of Patients with Parkinson's Disease.

Liu CF, Wang T, Zhan SQ, Geng DQ, Wang J, Liu J, Shang HF, Wang LJ, Chan P, Chen HB, Chen SD, Wang YP, Zhao ZX, Chaudhuri KR.

Chin Med J (Engl). 2018 Dec 20;131(24):2976-2985. doi: 10.4103/0366-6999.247210. No abstract available.


The study of exercise tests in paroxysmal kinesigenic dyskinesia.

Zhou HY, Zhan FX, Tian WT, Zhang C, Wang Y, Zhu ZY, Liu XL, Xu YQ, Luan XH, Huang XJ, Chen SD, Cao L.

Clin Neurophysiol. 2018 Nov;129(11):2435-2441. doi: 10.1016/j.clinph.2018.09.004. Epub 2018 Sep 15.


Current approaches for the management of Parkinson's disease in Chinese hospitals: a cross-sectional survey.

Wang G, Cui HL, Liu J, Xiao Q, Wang Y, Ma JF, Zhou HY, Pan J, Tan YY, Chen SD; Chinese Movement Disorders Society.

BMC Neurol. 2018 Aug 22;18(1):122. doi: 10.1186/s12883-018-1122-4.


Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's disease.

Liu SY, Zheng Z, Gu ZQ, Wang CD, Tang BS, Xu YM, Ma JH, Zhou YT, Feng T, Chen SD, Chan P; Chinese Parkinson Study Group.

Parkinsonism Relat Disord. 2018 Dec;57:72-76. doi: 10.1016/j.parkreldis.2018.08.007. Epub 2018 Aug 14.


The role of substantia nigra sonography in the differentiation of Parkinson's disease and multiple system atrophy.

Zhou HY, Huang P, Sun Q, Du JJ, Cui SS, Hu YY, Zhan WW, Wang Y, Xiao Q, Liu J, Tan YY, Chen SD.

Transl Neurodegener. 2018 Jul 23;7:15. doi: 10.1186/s40035-018-0121-0. eCollection 2018.


Detection of Microbial 16S rRNA Gene in the Blood of Patients With Parkinson's Disease.

Qian Y, Yang X, Xu S, Wu C, Qin N, Chen SD, Xiao Q.

Front Aging Neurosci. 2018 May 24;10:156. doi: 10.3389/fnagi.2018.00156. eCollection 2018. Erratum in: Front Aging Neurosci. 2019 Jan 30;11:4.


Lack of Association Between DNMT3B Polymorphisms and Sporadic Parkinson's Disease in a Han Chinese Population.

Pan H, Shen JY, Du JJ, Cui SS, Liu J, Lin YQ, He YX, Fu Y, Gao C, Li G, Chen SD, Ma JF.

Neurosci Bull. 2018 Oct;34(5):867-869. doi: 10.1007/s12264-018-0233-7. Epub 2018 May 14. No abstract available.


Association of Source of Memory Complaints and Increased Risk of Cognitive Impairment and Cognitive Decline: A Community-Based Study.

Qi XM, Gu L, Tang HD, Chen SD, Ma JF.

Chin Med J (Engl). 2018 Apr 20;131(8):894-898. doi: 10.4103/0366-6999.229904. Erratum in: Chin Med J (Engl). 2018 Jun 5;131(11):1320.


Substantia Nigra Echogenicity Associated with Clinical Subtypes of Parkinson's Disease.

Zhou HY, Huang P, Sun Q, Du JJ, Cui SS, Tan YY, Hu YY, Zhan WW, Wang Y, Xiao Q, Liu J, Chen SD.

J Parkinsons Dis. 2018;8(2):333-340. doi: 10.3233/JPD-171264.


Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review.

Tian WT, Liu XL, Xu YQ, Huang XJ, Zhou HY, Wang Y, Tang HD, Chen SD, Luan XH, Cao L.

Seizure. 2018 Apr;57:80-86. doi: 10.1016/j.seizure.2018.03.015. Epub 2018 Mar 14. Review.


RBD: a red flag for cognitive impairment in Parkinson's disease?

Lin YQ, Chen SD.

Sleep Med. 2018 Apr;44:38-44. doi: 10.1016/j.sleep.2018.01.006. Epub 2018 Jan 31. Review.


Alteration of the fecal microbiota in Chinese patients with Parkinson's disease.

Qian Y, Yang X, Xu S, Wu C, Song Y, Qin N, Chen SD, Xiao Q.

Brain Behav Immun. 2018 May;70:194-202. doi: 10.1016/j.bbi.2018.02.016. Epub 2018 Mar 2.


Expression of the gene coading for PGC-1α in peripheral blood leukocytes and related gene variants in patients with Parkinson's disease.

Yang XD, Qian YW, Xu SQ, Wan DY, Sun FH, Chen SD, Xiao Q.

Parkinsonism Relat Disord. 2018 Jun;51:30-35. doi: 10.1016/j.parkreldis.2018.02.037. Epub 2018 Feb 23.


Clinical Profile of Chinese Long-Term Parkinson's Disease Survivors With 10 Years of Disease Duration and Beyond.

Sun Q, Wang T, Jiang TF, Huang P, Wang Y, Xiao Q, Liu J, Chen SD.

Aging Dis. 2018 Feb 1;9(1):8-16. doi: 10.14336/AD.2017.0204. eCollection 2018 Feb.


Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population.

Che XQ, Zhao QH, Huang Y, Li X, Ren RJ, Chen SD, Guo QH, Wang G.

J Alzheimers Dis. 2018;61(4):1283-1288. doi: 10.3233/JAD-170692.


Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.

Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L.

Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22.


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