Dong S - Search Results

1

Flexible use of high-density oligonucleotide arrays for single-nucleotide polymorphism discovery and validation.

Dong S, Wang E, Hsie L, Cao Y, Chen X, Gingeras TR. Dong S, et al. Genome Res. 2001 Aug;11(8):1418-24. doi: 10.1101/gr.171101. Genome Res. 2001. PMID: 11483583 Free PMC article.

2

An exon 5 mutation (c.425G>C, p.Gly141Ala) in the SOD1 gene in a Chinese family associated with incomplete penetrance.

Dong SQ, Liu XN, Yang WB, Zhou YN, Wang JC, Chen XJ. Dong SQ, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Aug;21(5-6):473-476. doi: 10.1080/21678421.2020.1738496. Epub 2020 Mar 15. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32174179 No abstract available.

3

Mouse Nerve Growth Factor Injection and Progression Rate in Patients With Amyotrophic Lateral Sclerosis: An Observational Study.

Li JT, Dong SQ, Qian T, Yang WB, Chen XJ. Li JT, et al. Front Neurol. 2022 Feb 17;13:829569. doi: 10.3389/fneur.2022.829569. eCollection 2022. Front Neurol. 2022. PMID: 35250834 Free PMC article.

4

Prominent lower motor neuron involvement in patients with intermediate-length CAG repeats in ATXN3 gene.

Dong S, Zhu D, Yang W, Li J, Chen X. Dong S, et al. Neurol Sci. 2022 Dec;43(12):6993-6995. doi: 10.1007/s10072-022-06325-z. Epub 2022 Aug 23. Neurol Sci. 2022. PMID: 35997830 No abstract available.

5

Systematic Analysis of Chemokines Reveals CCL18 is a Prognostic Biomarker in Glioblastoma.

Gao W, Li Y, Zhang T, Lu J, Pan J, Qi Q, Dong S, Chen X, Su Z, Li J. Gao W, et al. Among authors: dong s. J Inflamm Res. 2022 Apr 28;15:2731-2743. doi: 10.2147/JIR.S357787. eCollection 2022. J Inflamm Res. 2022. PMID: 35509325 Free PMC article.

6

Role of Blood Neurofilaments in the Prognosis of Amyotrophic Lateral Sclerosis: A Meta-Analysis.

Zhou YN, Chen YH, Dong SQ, Yang WB, Qian T, Liu XN, Cheng Q, Wang JC, Chen XJ. Zhou YN, et al. Front Neurol. 2021 Oct 6;12:712245. doi: 10.3389/fneur.2021.712245. eCollection 2021. Front Neurol. 2021. PMID: 34690913 Free PMC article.

7

Expanding the Phenotypic and Genetic Spectrum of Neuromuscular Diseases Caused by DYNC1H1 Mutations.

Li JT, Dong SQ, Zhu DQ, Yang WB, Qian T, Liu XN, Chen XJ. Li JT, et al. Front Neurol. 2022 Jul 11;13:943324. doi: 10.3389/fneur.2022.943324. eCollection 2022. Front Neurol. 2022. PMID: 35899263 Free PMC article.

8

Case report: Novel compound heterozygous variants in the PANK2 gene in a Chinese patient diagnosed with ASD and ADHD.

Dong S, Tuo Y, Qi Z, Zhang Y, Liu X, Huang P, Chen X. Dong S, et al. Front Neurol. 2023 Apr 17;14:1118076. doi: 10.3389/fneur.2023.1118076. eCollection 2023. Front Neurol. 2023. PMID: 37139068 Free PMC article.

9

Presence of Rare Variants is Associated with Poorer Survival in Chinese Patients with Amyotrophic Lateral Sclerosis.

Dong S, Yin X, Wang K, Yang W, Li J, Wang Y, Zhou Y, Liu X, Wang J, Chen X. Dong S, et al. Phenomics. 2023 Feb 12;3(2):167-181. doi: 10.1007/s43657-022-00093-8. eCollection 2023 Apr. Phenomics. 2023. PMID: 37197644 Free PMC article.

10

Reduced dosage rituximab in the treatment of anti-N-methyl-d-aspartate receptor encephalitis: An observation study in Chinese patients.

Deng B, Yu H, Liu X, Yu X, Zhang X, Li X, Yang W, Dong S, Qiu Y, Chen X. Deng B, et al. Among authors: dong s. J Neuroimmunol. 2019 May 15;330:81-86. doi: 10.1016/j.jneuroim.2019.02.008. Epub 2019 Feb 18. J Neuroimmunol. 2019. PMID: 30851542

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