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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2005 1
2008 1
2010 2
2011 3
2012 4
2013 6
2014 2
2015 3
2016 1
2018 1
2019 4
2020 5
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32 results
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Page 1
Identification of two novel compound heterozygous CLCN1 mutations associated with autosomal recessive myotonia congenita.
Wei Z, Huaxing M, Xiaomei W, Juan W, Xueli C, Jing Z, Junhong G. Wei Z, et al. Among authors: xueli c. Neurol Res. 2019 Dec;41(12):1069-1074. doi: 10.1080/01616412.2019.1672392. Epub 2019 Sep 30. Neurol Res. 2019. PMID: 31566103
Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review.
Huang S, Zhang W, Chang X, Guo J. Huang S, et al. Among authors: chang x. Channels (Austin). 2019 Dec;13(1):110-119. doi: 10.1080/19336950.2019.1600967. Channels (Austin). 2019. PMID: 30931713 Free PMC article. Review.
Muscle ultrasonography in the diagnosis of amyotrophic lateral sclerosis.
Juan W, Fang L, Qi W, Jing M, Shan H, Jing Z, Xueli C, Wei Z, Junhong G. Juan W, et al. Among authors: xueli c. Neurol Res. 2020 Jun;42(6):458-462. doi: 10.1080/01616412.2020.1738100. Epub 2020 Mar 5. Neurol Res. 2020. PMID: 32138623
Association between asymptomatic carotid stenosis and cognitive function: a systematic review.
Chang XL, Zhou HQ, Lei CY, Wu B, Chen YC, Hao ZL, Dong W, Liu M. Chang XL, et al. Neurosci Biobehav Rev. 2013 Sep;37(8):1493-9. doi: 10.1016/j.neubiorev.2013.05.011. Epub 2013 May 30. Neurosci Biobehav Rev. 2013. PMID: 23727050 Review.
Mutations in GBA and risk of Parkinson's disease: a meta-analysis based on 25 case-control studies.
Mao X, Wang T, Peng R, Chang X, Li N, Gu Y, Zhao D, Liao Q, Liu M. Mao X, et al. Among authors: chang x. Neurol Res. 2013 Oct;35(8):873-8. doi: 10.1179/1743132813Y.0000000224. Epub 2013 May 14. Neurol Res. 2013. PMID: 23676350 Review.
A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations.
Chang X, Wu Y, Zhou J, Meng H, Zhang W, Guo J. Chang X, et al. Medicine (Baltimore). 2020 Jan;99(5):e18634. doi: 10.1097/MD.0000000000018634. Medicine (Baltimore). 2020. PMID: 32000367 Free PMC article.
Functional parkin promoter polymorphism in Parkinson's disease: new data and meta-analysis.
Chang XL, Mao XY, Li HH, Zhang JH, Li NN, Burgunder JM, Peng R, Tan EK. Chang XL, et al. J Neurol Sci. 2011 Mar 15;302(1-2):68-71. doi: 10.1016/j.jns.2010.11.023. Epub 2010 Dec 21. J Neurol Sci. 2011. PMID: 21176923 Review.
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