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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 4
2003 15
2004 5
2005 4
2006 11
2007 13
2008 8
2009 10
2010 11
2011 9
2012 11
2013 8
2014 13
2015 17
2016 9
2017 13
2018 22
2019 28
2020 20
2021 23
2022 28
2023 18
2024 10

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278 results

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Page 1
Potassium channels and epilepsy.
Gao K, Lin Z, Wen S, Jiang Y. Gao K, et al. Among authors: jiang y. Acta Neurol Scand. 2022 Dec;146(6):699-707. doi: 10.1111/ane.13695. Epub 2022 Oct 12. Acta Neurol Scand. 2022. PMID: 36225112 Review.
International Consensus Recommendations for the Treatment of Pediatric NMDAR Antibody Encephalitis.
Nosadini M, Thomas T, Eyre M, Anlar B, Armangue T, Benseler SM, Cellucci T, Deiva K, Gallentine W, Gombolay G, Gorman MP, Hacohen Y, Jiang Y, Lim BC, Muscal E, Ndondo A, Neuteboom R, Rostásy K, Sakuma H, Sharma S, Tenembaum SN, Van Mater HA, Wells E, Wickstrom R, Yeshokumar AK, Irani SR, Dalmau J, Lim M, Dale RC. Nosadini M, et al. Among authors: jiang y. Neurol Neuroimmunol Neuroinflamm. 2021 Jul 22;8(5):e1052. doi: 10.1212/NXI.0000000000001052. Print 2021 Jul. Neurol Neuroimmunol Neuroinflamm. 2021. PMID: 34301820 Free PMC article.
Use and Safety of Immunotherapeutic Management of N-Methyl-d-Aspartate Receptor Antibody Encephalitis: A Meta-analysis.
Nosadini M, Eyre M, Molteni E, Thomas T, Irani SR, Dalmau J, Dale RC, Lim M; International NMDAR Antibody Encephalitis Consensus Group; Anlar B, Armangue T, Benseler S, Cellucci T, Deiva K, Gallentine W, Gombolay G, Gorman MP, Hacohen Y, Jiang Y, Lim BC, Muscal E, Ndondo A, Neuteboom R, Rostásy K, Sakuma H, Sartori S, Sharma S, Tenembaum SN, Van Mater HA, Wells E, Wickstrom R, Yeshokumar AK. Nosadini M, et al. Among authors: jiang y. JAMA Neurol. 2021 Nov 1;78(11):1333-1344. doi: 10.1001/jamaneurol.2021.3188. JAMA Neurol. 2021. PMID: 34542573 Free PMC article.
SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.
Zeng Q, Yang Y, Duan J, Niu X, Chen Y, Wang D, Zhang J, Chen J, Yang X, Li J, Yang Z, Jiang Y, Liao J, Zhang Y. Zeng Q, et al. Among authors: jiang y. Front Mol Neurosci. 2022 Mar 30;15:809951. doi: 10.3389/fnmol.2022.809951. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35431799 Free PMC article.
A phase 2, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of soticlestat as adjunctive therapy in pediatric patients with Dravet syndrome or Lennox-Gastaut syndrome (ELEKTRA).
Hahn CD, Jiang Y, Villanueva V, Zolnowska M, Arkilo D, Hsiao S, Asgharnejad M, Dlugos D. Hahn CD, et al. Among authors: jiang y. Epilepsia. 2022 Oct;63(10):2671-2683. doi: 10.1111/epi.17367. Epub 2022 Aug 4. Epilepsia. 2022. PMID: 35841234 Free PMC article. Clinical Trial.
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Vlaskamp DRM, Shaw BJ, Burgess R, Mei D, Montomoli M, Xie H, Myers CT, Bennett MF, XiangWei W, Williams D, Maas SM, Brooks AS, Mancini GMS, van de Laar IMBH, van Hagen JM, Ware TL, Webster RI, Malone S, Berkovic SF, Kalnins RM, Sicca F, Korenke GC, van Ravenswaaij-Arts CMA, Hildebrand MS, Mefford HC, Jiang Y, Guerrini R, Scheffer IE. Vlaskamp DRM, et al. Among authors: jiang y. Neurology. 2019 Jan 8;92(2):e96-e107. doi: 10.1212/WNL.0000000000006729. Epub 2018 Dec 12. Neurology. 2019. PMID: 30541864 Free PMC article.
Genetic generalized epilepsies.
Mullen SA, Berkovic SF; ILAE Genetics Commission. Mullen SA, et al. Epilepsia. 2018 Jun;59(6):1148-1153. doi: 10.1111/epi.14042. Epub 2018 May 9. Epilepsia. 2018. PMID: 29741207 Review.
Editorial: Sub-molecular mechanism of genetic epilepsy.
Liao WP, Chen Q, Jiang YW, Luo S, Liu XR. Liao WP, et al. Front Mol Neurosci. 2022 Jul 26;15:958747. doi: 10.3389/fnmol.2022.958747. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35959103 Free PMC article. No abstract available.
CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia.
Tan D, Wei C, Chen Z, Huang Y, Deng J, Li J, Liu Y, Bao X, Xu J, Hu Z, Wang S, Fan Y, Jiang Y, Wu Y, Wu Y, Wang S, Liu P, Zhang Y, Yang Z, Jiang Y, Zhang H, Hong D, Zhong N, Jiang H, Xiong H. Tan D, et al. Among authors: jiang y. Mov Disord. 2023 Jul;38(7):1282-1293. doi: 10.1002/mds.29412. Epub 2023 May 6. Mov Disord. 2023. PMID: 37148549
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. Granadillo JL, et al. Among authors: jiang y. J Med Genet. 2020 Oct;57(10):717-724. doi: 10.1136/jmedgenet-2019-106470. Epub 2020 Mar 9. J Med Genet. 2020. PMID: 32152250
278 results