Wang J - Search Results

1

Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein-Associated Neurodegeneration.

Yang Y, Zhang S, Yang W, Wei T, Hao W, Cheng T, Wang J, Dong W, Qian N. Yang Y, et al. Among authors: wang j. Front Genet. 2022 Mar 30;13:852374. doi: 10.3389/fgene.2022.852374. eCollection 2022. Front Genet. 2022. PMID: 35432442 Free PMC article.

2

Wilson disease patient with rare heterozygous mutations in ATP7B accompanied by distinctive nocturnal enuresis: A case report.

Zhang S, Li L, Wang J. Zhang S, et al. Among authors: wang j. Medicine (Baltimore). 2020 Jul 10;99(28):e20997. doi: 10.1097/MD.0000000000020997. Medicine (Baltimore). 2020. PMID: 32664103 Free PMC article.

3

Identification of mutations in the ATP7B gene in 14 Wilson disease children: Case series.

Wang J, Tang L, Xu A, Zhang S, Jiang H, Pei P, Li H, Lv T, Yang Y, Qian N, Naidu K, Yang W. Wang J, et al. Medicine (Baltimore). 2021 Apr 23;100(16):e25463. doi: 10.1097/MD.0000000000025463. Medicine (Baltimore). 2021. PMID: 33879678 Free PMC article.

4

Case Report: Late-Onset Autosomal Recessive Cerebellar Ataxia Associated With SYNE1 Mutation in a Chinese Family.

Qian N, Wei T, Yang W, Wang J, Zhang S, Jin S, Dong W, Hao W, Yang Y, Huang R. Qian N, et al. Among authors: wang j. Front Genet. 2022 Feb 23;13:795188. doi: 10.3389/fgene.2022.795188. eCollection 2022. Front Genet. 2022. PMID: 35281832 Free PMC article.

5

Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.

Jia W, Luo Y, Wang J, Yang Y, Yang W, Zhang X. Jia W, et al. Among authors: wang j. Neurodegener Dis. 2021;21(5-6):126-131. doi: 10.1159/000524784. Epub 2022 May 24. Neurodegener Dis. 2021. PMID: 35609511

6

Clinical manifestations and genetic analysis of a newborn with Arboleda-Tham syndrome.

Zeng F, Yang Y, Xu Z, Wang Z, Ke H, Zhang J, Dong T, Yang W, Wang J. Zeng F, et al. Among authors: wang z, wang j. Front Genet. 2022 Oct 25;13:990098. doi: 10.3389/fgene.2022.990098. eCollection 2022. Front Genet. 2022. PMID: 36386811 Free PMC article.

7

Discussion on the Mechanism of Gandoufumu Decoction Attenuates Liver Damage of Wilson's Disease by Inhibiting Autophagy through the PI3K/Akt/mTOR Pathway Based on Network Pharmacology and Experimental Verification.

Tang L, Zhao C, Zhang J, Dong T, Chen H, Wei T, Wang J, Yang W. Tang L, et al. Among authors: wang j. Mediators Inflamm. 2023 Jun 15;2023:3236911. doi: 10.1155/2023/3236911. eCollection 2023. Mediators Inflamm. 2023. PMID: 37362448 Free PMC article.

8

Clinical and genetic characterization of patients with late onset Wilson's disease.

Yang W, Yang Y, Wang H, Wang J, Zhang S. Yang W, et al. Among authors: wang h, wang j. NPJ Genom Med. 2024 Dec 24;9(1):71. doi: 10.1038/s41525-024-00459-z. NPJ Genom Med. 2024. PMID: 39719440 Free PMC article.

9

Association between osteoporosis or osteopenia and taking antiplatelet agents in general US population of NHANES.

Lv H, Wang J, Zhu Y, Hu Z, Wang Z, Qiao M, Jiang T. Lv H, et al. Among authors: wang j, wang z. Front Endocrinol (Lausanne). 2022 Aug 9;13:945159. doi: 10.3389/fendo.2022.945159. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36017309 Free PMC article.

10

Study on the Mechanism of Compound Kidney-Invigorating Granule for Osteoporosis based on Network Pharmacology and Experimental Verification.

Lv H, Wang J, Zhu Y, Jiang T. Lv H, et al. Among authors: wang j. Evid Based Complement Alternat Med. 2022 Jan 4;2022:6453501. doi: 10.1155/2022/6453501. eCollection 2022. Evid Based Complement Alternat Med. 2022. PMID: 35027934 Free PMC article.

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