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Data on mutations and Clinical features in SCN1A or SCN2A gene.
Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Kong Y, et al. Data Brief. 2018 Aug 30;22:492-501. doi: 10.1016/j.dib.2018.08.122. eCollection 2019 Feb. Data Brief. 2018. PMID: 30619928 Free PMC article.
Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China.
Yang L, Wei Z, Chen X, Hu L, Peng X, Wang J, Lu C, Kong Y, Dong X, Ni Q, Lu Y, Wu B, Wang H, Meirelles K, Tian X, Zhang J, Chang F, Liu L, Li C, You W, Cheng G, Wang L, Cao Y, Chen C, Fang P, Tang S, Zhou W. Yang L, et al. Among authors: kong y. Clin Genet. 2022 Jan;101(1):101-109. doi: 10.1111/cge.14075. Epub 2021 Oct 25. Clin Genet. 2022. PMID: 34671977
Incidence of Neonatal Seizures in China Based on Electroencephalogram Monitoring in Neonatal Neurocritical Care Units.
Yan K, Cheng G, Zhou W, Xiao F, Zhang C, Wang L, Zhang P, Lu C, Kong Y, Wang X, Zhou Y, Lu W, Tang J, Song X, Wei Q, Meng D, Yao L, Zhuang D, Qu L, Xu Q, Yin Z, Su L, Wan J, Si Y, Fujioka K, Mussap M, Kanungo S, Bhandari V, Huang W, Pan X, Zhou W; China Neonatal Neuro-Critical Care Network group. Yan K, et al. Among authors: kong y. JAMA Netw Open. 2023 Jul 3;6(7):e2326301. doi: 10.1001/jamanetworkopen.2023.26301. JAMA Netw Open. 2023. PMID: 37505497 Free PMC article.
Tenecteplase Thrombolysis for Stroke up to 24 Hours After Onset With Perfusion Imaging Selection: The CHABLIS-T II Randomized Clinical Trial.
Cheng X, Hong L, Lin L, Churilov L, Ling Y, Yang N, Fu J, Lu G, Yue Y, Zhang J, Wang F, Wang Z, Zhao Y, Zhou X, Peng Z, Wu D, Zhao L, Zhai Q, Yu X, Fang Q, Shao X, Tang Y, Zhang D, Geng Y, Zhang Y, Fan B, Zhang B, Yin C, Chen Y, Zhang Y, Liu X, Li S, Yang L, Parsons M, Dong Q; CHABLIS-T II Collaborators. Cheng X, et al. Stroke. 2025 Jan 2. doi: 10.1161/STROKEAHA.124.048375. Online ahead of print. Stroke. 2025. PMID: 39744861
6,046 results