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2019 | 3 |
2022 | 3 |
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xu, wen xiao
(12 results)?
GSN gene frameshift mutations in Alzheimer's disease.
J Neurol Neurosurg Psychiatry. 2023 Jun;94(6):436-447. doi: 10.1136/jnnp-2022-330465. Epub 2023 Jan 17.
J Neurol Neurosurg Psychiatry. 2023.
PMID: 36650038
Free PMC article.
Propylthiouracil-induced organizing pneumonia: A case report.
Xiao XW, An J, Hu CP, Luo BL.
Xiao XW, et al.
Medicine (Baltimore). 2019 Jul;98(27):e16284. doi: 10.1097/MD.0000000000016284.
Medicine (Baltimore). 2019.
PMID: 31277157
Free PMC article.
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Association Between Serum Vitamins and the Risk of Alzheimer's Disease in Chinese Population.
Liu XX, Wu PF, Liu YZ, Jiang YL, Wan MD, Xiao XW, Yang QJ, Jiao B, Liao XX, Wang JL, Liu SH, Zhang X, Shen L.
Liu XX, et al. Among authors: xiao xw.
J Alzheimers Dis. 2022;85(2):829-836. doi: 10.3233/JAD-215104.
J Alzheimers Dis. 2022.
PMID: 34864672
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Analysis of Salivary Microbiome in Patients with Alzheimer's Disease.
Liu XX, Jiao B, Liao XX, Guo LN, Yuan ZH, Wang X, Xiao XW, Zhang XY, Tang BS, Shen L.
Liu XX, et al. Among authors: xiao xw.
J Alzheimers Dis. 2019;72(2):633-640. doi: 10.3233/JAD-190587.
J Alzheimers Dis. 2019.
PMID: 31594229
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Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study.
Wen YF, Xiao XW, Zhou L, Jiang YL, Zhu Y, Guo LN, Wang X, Liu H, Zhou YF, Wang JL, Liao XX, Shen L, Jiao B.
Wen YF, et al. Among authors: xiao xw.
Neural Regen Res. 2022 Mar;17(3):682-689. doi: 10.4103/1673-5374.321000.
Neural Regen Res. 2022.
PMID: 34380910
Free PMC article.
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Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer's disease.
Wan MD, Liu H, Liu XX, Zhang WW, Xiao XW, Zhang SZ, Jiang YL, Zhou H, Liao XX, Zhou YF, Tang BS, Wang JL, Guo JF, Jiao B, Shen L.
Wan MD, et al. Among authors: xiao xw.
Front Aging Neurosci. 2022 Jul 29;14:906519. doi: 10.3389/fnagi.2022.906519. eCollection 2022.
Front Aging Neurosci. 2022.
PMID: 35966797
Free PMC article.
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Novel ATL1 mutation in a Chinese family with hereditary spastic paraplegia: A case report and review of literature.
Xiao XW, Du J, Jiao B, Liao XX, Zhou L, Liu XX, Yuan ZH, Guo LN, Wang X, Shen L, Lin ZY.
Xiao XW, et al.
World J Clin Cases. 2019 Jun 6;7(11):1358-1366. doi: 10.12998/wjcc.v7.i11.1358.
World J Clin Cases. 2019.
PMID: 31236401
Free PMC article.
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