缩写名/全名 |
MOVEMENT DISORD
MOVEMENT DISORDERS |
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ISSN号 | 0885-3185 | ||||||||||||||||||||
研究方向 | 医学-临床神经学 | ||||||||||||||||||||
影响因子 | 2015:6.01, 2016:7.072, 2017:8.324, 2018:8.061, 2019:8.679, | ||||||||||||||||||||
出版国家 | UNITED STATES | ||||||||||||||||||||
出版周期 | Semimonthly | ||||||||||||||||||||
年文章数 | 170 | ||||||||||||||||||||
出版年份 | 1986 | ||||||||||||||||||||
是否OA | No | ||||||||||||||||||||
审稿周期(仅供参考) | 平均12月 |
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录用比例 | 约25% | ||||||||||||||||||||
投稿链接 | http://mc.manuscriptcentral.com/mds | ||||||||||||||||||||
投稿官网 | http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 | ||||||||||||||||||||
h-index | 174 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0885-3185%5BISSN%5D | ||||||||||||||||||||
中科院SCI期刊分区 ( 2018年新版本) |
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中科院SCI期刊分区 ( 2020年新版本) |
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中国学者近期发表的论文 | |
1. | Familial ataxia, tremor, and dementia in a polish family with a novel mutation in the CCDC88C gene. Author: Leńska-Mieciek M1, Charzewska A2, Królicki L3, Hoffman-Zacharska D2, Chen ZS4, Lau KF4, Chan HYE4,5, Gambin T2, Fiszer U1. Journal: Mov Disord. 2019 Jan;34(1):142-144. doi: 10.1002/mds.27536. Epub 2018 Nov 6. PubMed DOI |
2. | Serum soluble lymphocyte activation gene-3 as a diagnostic biomarker in Parkinson's disease: A pilot multicenter study. Author: Cui SS1, Du JJ1, Liu SH2, Meng J3, Lin YQ1, Li G1, He YX1, Zhang PC1, Chen S1, Wang G1. Journal: Mov Disord. 2019 Jan;34(1):138-141. doi: 10.1002/mds.27569. Epub 2018 Nov 28. PubMed DOI |
3. | Evaluation of MYORG mutations as a novel cause of primary familial brain calcification. Author: Chen Y1, Fu F2, Chen S1,3, Cen Z1, Tang H1,4, Huang J1, Xie F1,5, Zheng X1,6, Yang D1, Wang H1, Huang X7, Zhang Y1, Zhou Y8, Liu JY9, Luo W1. Journal: Mov Disord. 2019 Feb;34(2):291-297. doi: 10.1002/mds.27582. Epub 2018 Dec 27. PubMed DOI |
4. | Reproducible detection of nigral iron deposition in 2 Parkinson's disease cohorts. Author: Langley J1, He N2, Huddleston DE3, Chen S4, Yan F2, Crosson B3,5,6, Factor S3, Hu X1,7. Journal: Mov Disord. 2019 Mar;34(3):416-419. doi: 10.1002/mds.27608. Epub 2018 Dec 30. PubMed DOI |
5. | Regional morphometric abnormalities and clinical relevance in Wilson's disease. Author: Zou L1, Song Y2, Zhou X3, Chu J4, Tang X1. Journal: Mov Disord. 2019 Apr;34(4):545-554. doi: 10.1002/mds.27641. Epub 2019 Feb 28. PubMed DOI |
6. | Enhanced Na+ -K+ -2Cl- cotransporter 1 underlies motor dysfunction in huntington's disease. Author: Hsu YT1,2, Chang YG3,4, Liu YC3, Wang KY3, Chen HM5, Lee DJ1, Yang SS6, Tsai CH1,2, Lien CC3,7, Chern Y1,3,5. Journal: Mov Disord. 2019 Mar 6. doi: 10.1002/mds.27651. [Epub ahead of print] PubMed DOI |
7. | Modifiable risk factors for cognitive impairment in Parkinson's disease: A systematic review and meta-analysis of prospective cohort studies. Author: Guo Y1, Xu W1, Liu FT2, Li JQ1, Cao XP1, Tan L1, Wang J2, Yu JT2. Journal: Mov Disord. 2019 Mar 14. doi: 10.1002/mds.27665. [Epub ahead of print] PubMed DOI |
8. | Mild cognitive impairment in de novo Parkinson's disease: A neuromelanin MRI study in locus coeruleus. Author: Li Y1, Wang C1, Wang J2,3, Zhou Y1, Ye F2,3, Zhang Y4, Cheng X1, Huang Z1, Liu K2,3, Fei G1, Zhong C1, Zeng M2,3, Jin L1. Journal: Mov Disord. 2019 Apr 2. doi: 10.1002/mds.27682. [Epub ahead of print] PubMed DOI |
9. | LRP10 in autosomal-dominant Parkinson's disease. Author: Chen Y1, Cen Z1, Zheng X1,2, Pan Q1,3, Chen X1,4, Zhu L5, Chen S1,6, Wu H1,7, Xie F1,8, Wang H1, Yang D1, Wang L1,4, Zhang B1, Luo W1. Journal: Mov Disord. 2019 Apr 9. doi: 10.1002/mds.27693. [Epub ahead of print] PubMed DOI |
10. | l-Dopa-free learned dyskinetic behavior in a Parkinson's primate model. Author: Li Q1,2, Fernagut PO3, Bezard E1,2,4,5. Journal: Mov Disord. 2019 May 13. doi: 10.1002/mds.27715. [Epub ahead of print] PubMed DOI |
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