Wang L - Search Results

1

Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.

He R, Li H, Sun Y, Chen M, Wang L, Zhu Y, Zhang C. He R, et al. Among authors: wang l. BMC Neurol. 2020 Mar 2;20(1):72. doi: 10.1186/s12883-020-01660-0. BMC Neurol. 2020. PMID: 32122318 Free PMC article.

2

Long-term engraftment of myogenic progenitors from adipose-derived stem cells and muscle regeneration in dystrophic mice.

Zhang Y, Zhu Y, Li Y, Cao J, Zhang H, Chen M, Wang L, Zhang C. Zhang Y, et al. Among authors: wang l. Hum Mol Genet. 2015 Nov 1;24(21):6029-40. doi: 10.1093/hmg/ddv316. Epub 2015 Aug 11. Hum Mol Genet. 2015. PMID: 26264578

3

Abnormal Neural Progenitor Cells Differentiated from Induced Pluripotent Stem Cells Partially Mimicked Development of TSC2 Neurological Abnormalities.

Li Y, Cao J, Chen M, Li J, Sun Y, Zhang Y, Zhu Y, Wang L, Zhang C. Li Y, et al. Among authors: wang l. Stem Cell Reports. 2017 Apr 11;8(4):883-893. doi: 10.1016/j.stemcr.2017.02.020. Epub 2017 Mar 23. Stem Cell Reports. 2017. PMID: 28344003 Free PMC article.

4

Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.

Wang L, Chen M, He R, Sun Y, Yang J, Xiao L, Cao J, Zhang H, Zhang C. Wang L, et al. Front Neurol. 2017 May 8;8:196. doi: 10.3389/fneur.2017.00196. eCollection 2017. Front Neurol. 2017. PMID: 28533764 Free PMC article.

5

Surgical Management and Outcomes of Intracranial Chondromas: a Single-Center Case Series of 66 Patients.

Weng JC, Li D, Li H, Ma JP, Tian KB, Wang L, Zhang LW, Jia W, Wu Z, Zhang JT. Weng JC, et al. Among authors: wang l. World Neurosurg. 2017 Dec;108:264-277. doi: 10.1016/j.wneu.2017.08.151. Epub 2017 Sep 1. World Neurosurg. 2017. PMID: 28867324

6

[Analysis of SMN1 gene mutations in 78 patients with spinal muscular atrophy].

Li J, Zhu Y, Zhan Y, Li Y, Chen M, Wang L, He R, Zhang C. Li J, et al. Among authors: wang l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):658-661. doi: 10.3760/cma.j.issn.1003-9406.2017.05.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981927 Chinese.

7

Ratio of Creatine Kinase to Alanine Aminotransferase as a Biomarker of Acute Liver Injury in Dystrophinopathy.

Wang L, Chen M, Xu M, Li J, Feng P, He R, Zhu Y, Li H, Lin J, Zhang C. Wang L, et al. Dis Markers. 2018 Jun 19;2018:6484610. doi: 10.1155/2018/6484610. eCollection 2018. Dis Markers. 2018. PMID: 30018675 Free PMC article.

8

The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients.

Wang L, Zhang VW, Li S, Li H, Sun Y, Li J, Zhu Y, He R, Lin J, Zhang C. Wang L, et al. Orphanet J Rare Dis. 2018 Aug 14;13(1):133. doi: 10.1186/s13023-018-0859-6. Orphanet J Rare Dis. 2018. PMID: 30107846 Free PMC article.

9

HLA Polymorphism Affects Risk of de novo Mutation of dystrophin Gene and Clinical Severity of Duchenne Muscular Dystrophy in a Southern Chinese Population.

Li H, Xiao L, Wang L, Lin J, Luo M, Chen M, He R, Zhu Y, Zhang C. Li H, et al. Among authors: wang l. Front Neurol. 2018 Nov 15;9:970. doi: 10.3389/fneur.2018.00970. eCollection 2018. Front Neurol. 2018. PMID: 30498470 Free PMC article.

10

Genotypes and Phenotypes of DMD Small Mutations in Chinese Patients With Dystrophinopathies.

Wang L, Xu M, Li H, He R, Lin J, Zhang C, Zhu Y. Wang L, et al. Front Genet. 2019 Feb 18;10:114. doi: 10.3389/fgene.2019.00114. eCollection 2019. Front Genet. 2019. PMID: 30833962 Free PMC article.

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