Wang X - Search Results

1

Epilepsy in Dravet Syndrome-Current and Future Therapeutic Opportunities.

Gao C, Pielas M, Jiao F, Mei D, Wang X, Kotulska K, Jozwiak S. Gao C, et al. Among authors: wang x. J Clin Med. 2023 Mar 27;12(7):2532. doi: 10.3390/jcm12072532. J Clin Med. 2023. PMID: 37048615 Free PMC article. Review.

2

Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex-Current Views on Their Pathogenesis and Management.

Gao C, Zabielska B, Jiao F, Mei D, Wang X, Kotulska K, Jozwiak S. Gao C, et al. Among authors: wang x. J Clin Med. 2023 Jan 26;12(3):956. doi: 10.3390/jcm12030956. J Clin Med. 2023. PMID: 36769603 Free PMC article. Review.

3

A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature review.

Liu M, Li B, Wang X, Li D, Xie Z, Li Y, Gao Y, Chen B, Zhang H, Wang Y, Gao C. Liu M, et al. Among authors: wang x, wang y. Ann Hum Genet. 2023 Jul;87(4):158-165. doi: 10.1111/ahg.12503. Epub 2023 Mar 10. Ann Hum Genet. 2023. PMID: 36896784 Review.

4

[Clinical characteristics and genetic variant analysis of a child with Snijders Blok-Campeau syndrome].

Li Y, Wang X, Liu M, Gao Y, Chen B, Mei D, Zhang H, Gao C. Li Y, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Apr 10;40(4):402-407. doi: 10.3760/cma.j.cn511374-20221108-00768. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36972932 Chinese.

5

Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant.

Gu Y, Mei D, Wang X, Ma A, Kong J, Zhang Y. Gu Y, et al. Among authors: wang x. Front Neurol. 2023 May 9;14:1135044. doi: 10.3389/fneur.2023.1135044. eCollection 2023. Front Neurol. 2023. PMID: 37228410 Free PMC article.

6

Functional Evaluation of a Novel GRIN2B Missense Variant Associated with Epilepsy and Intellectual Disability.

Wang X, Mei D, Gou L, Zhao S, Gao C, Guo J, Luo S, Guo B, Yang Z, Wang Q, Tan T, Zhang Y. Wang X, et al. Among authors: wang q. Neuroscience. 2023 Aug 21;526:107-120. doi: 10.1016/j.neuroscience.2023.06.018. Epub 2023 Jun 28. Neuroscience. 2023. PMID: 37385334 Free article.

7

GABA_B1 receptor knockdown in prefrontal cortex induces behavioral aberrations associated with autism spectrum disorder in mice.

Wang X, Zhao Z, Guo J, Mei D, Duan Y, Zhang Y, Gou L. Wang X, et al. Brain Res Bull. 2023 Oct 1;202:110755. doi: 10.1016/j.brainresbull.2023.110755. Epub 2023 Sep 7. Brain Res Bull. 2023. PMID: 37678443 Free article.

8

Restoration of nNOS Expression Rescues Autistic-Like Phenotypes Through Normalization of AMPA Receptor-Mediated Neurotransmission.

Wang X, Zhang Y, Luo S, Zhao K, Gao C, Mei D, Duan Y, Hu S. Wang X, et al. Mol Neurobiol. 2024 Sep;61(9):6599-6612. doi: 10.1007/s12035-024-03997-w. Epub 2024 Feb 8. Mol Neurobiol. 2024. PMID: 38329681

9

Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3.

Li W, Li Z, Fu J, Xu K, Mei D, Wang X, Li T, Du X. Li W, et al. Among authors: wang x. Front Genet. 2024 Sep 2;15:1382275. doi: 10.3389/fgene.2024.1382275. eCollection 2024. Front Genet. 2024. PMID: 39286456 Free PMC article.

10

Alterations of Thyroid Hormone Levels in Children with Intellectual Disability.

Zhao Z, Su M, Wang D, Ye J, Wang XN. Zhao Z, et al. Neuropediatrics. 2023 Feb;54(1):53-57. doi: 10.1055/a-1959-8959. Epub 2022 Oct 12. Neuropediatrics. 2023. PMID: 36223878

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