Wang SM - Search Results

1

[Mutational analysis of the methyl-CpG-binding protein 2 (MECP2) gene in male autism patients].

Wang SM, Li M, Yang YL, Pan H, Liu J, Pan KF, Bu DF. Wang SM, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2013 Apr 18;45(2):197-201. Beijing Da Xue Xue Bao Yi Xue Ban. 2013. PMID: 23591336 Free article. Chinese.

2

Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report.

Wang Y, Chen Y, Wang SM, Liu X, Gu YN, Feng Z. Wang Y, et al. Among authors: wang sm. BMC Med Genet. 2020 Nov 11;21(1):222. doi: 10.1186/s12881-020-01157-0. BMC Med Genet. 2020. PMID: 33176713 Free PMC article.

3

Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay.

Wang S, Cui D, Ling X, Hou Y, Sun J. Wang S, et al. Psychiatr Genet. 2023 Oct 1;33(5):206-212. doi: 10.1097/YPG.0000000000000345. Epub 2023 Jun 12. Psychiatr Genet. 2023. PMID: 37706497

4

[No title available]

[No authors listed] [No authors listed] PMID: 37706522

5

Clinical and genetic characteristics of pyridoxine-dependent epilepsy: Case series report of three Chinese patients with phenotypic variability.

Wang S, Sun J, Tu Y, Zhu L, Feng Z. Wang S, et al. Exp Ther Med. 2017 Sep;14(3):1989-1992. doi: 10.3892/etm.2017.4735. Epub 2017 Jul 9. Exp Ther Med. 2017. PMID: 28962114 Free PMC article.

6

Beyond CMV: Exploring the multifactorial immunological Landscape in depression.

Lyu Q, Zhou E, Liu LN, Wang SM, Cui HF, Bai TY. Lyu Q, et al. Among authors: wang sm. Brain Behav Immun. 2025 Jan 20;125:332-333. doi: 10.1016/j.bbi.2025.01.011. Online ahead of print. Brain Behav Immun. 2025. PMID: 39842558 No abstract available.

7

[Status and prospect of esophageal cancer screening].

Li MJ, Chen R, Wang SM, Wei WW. Li MJ, et al. Among authors: wang sm. Zhonghua Zhong Liu Za Zhi. 2025 Jan 23;47(1):94-99. doi: 10.3760/cma.j.cn112152-20231024-00231. Zhonghua Zhong Liu Za Zhi. 2025. PMID: 39828586 Review. Chinese.

8

Reoperations as an Outcome Indicator for Developmental Dysplasia of the Hip Treated at Walking Age.

Chang CH, Hung CL, Lee WC, Kao HK, Wang SM, Kuo KN. Chang CH, et al. Among authors: wang sm. J Bone Joint Surg Am. 2025 Jan 17. doi: 10.2106/JBJS.24.00486. Online ahead of print. J Bone Joint Surg Am. 2025. PMID: 39823351

9

Association analysis of genetic polymorphisms of METTL3 with clinical outcomes in a Chinese pediatric population with primary brain tumors.

Wang SM, Kong XY, Zhao DQ, Li M. Wang SM, et al. Gene. 2025 Mar 15;941:149232. doi: 10.1016/j.gene.2025.149232. Epub 2025 Jan 10. Gene. 2025. PMID: 39800197

10

Effects of SCT genetic polymorphisms on methotrexate concentrations and toxicities in Chinese children with acute lymphoblastic leukemia.

Li M, Zhao DQ, Kong XY, Wang SM. Li M, et al. Among authors: wang sm. Leuk Lymphoma. 2025 Jan 11:1-11. doi: 10.1080/10428194.2025.2451059. Online ahead of print. Leuk Lymphoma. 2025. PMID: 39798147

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