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

Year Number of Results
2004 2
2005 2
2006 7
2007 8
2008 7
2009 7
2010 12
2011 12
2012 14
2013 11
2014 16
2015 12
2016 11
2017 11
2018 17
2019 14
2020 13
2021 13
2022 11
2023 14
2024 2

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187 results

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Page 1
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development.
Chung C, Yang X, Bae T, Vong KI, Mittal S, Donkels C, Westley Phillips H, Li Z, Marsh APL, Breuss MW, Ball LL, Garcia CAB, George RD, Gu J, Xu M, Barrows C, James KN, Stanley V, Nidhiry AS, Khoury S, Howe G, Riley E, Xu X, Copeland B, Wang Y, Kim SH, Kang HC, Schulze-Bonhage A, Haas CA, Urbach H, Prinz M, Limbrick DD Jr, Gurnett CA, Smyth MD, Sattar S, Nespeca M, Gonda DD, Imai K, Takahashi Y, Chen HH, Tsai JW, Conti V, Guerrini R, Devinsky O, Silva WA Jr, Machado HR, Mathern GW, Abyzov A, Baldassari S, Baulac S; Focal Cortical Dysplasia Neurogenetics Consortium; Brain Somatic Mosaicism Network; Gleeson JG. Chung C, et al. Among authors: kang hc. Nat Genet. 2023 Feb;55(2):209-220. doi: 10.1038/s41588-022-01276-9. Epub 2023 Jan 12. Nat Genet. 2023. PMID: 36635388 Free PMC article.
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group.
Kossoff EH, Zupec-Kania BA, Auvin S, Ballaban-Gil KR, Christina Bergqvist AG, Blackford R, Buchhalter JR, Caraballo RH, Cross JH, Dahlin MG, Donner EJ, Guzel O, Jehle RS, Klepper J, Kang HC, Lambrechts DA, Liu YMC, Nathan JK, Nordli DR Jr, Pfeifer HH, Rho JM, Scheffer IE, Sharma S, Stafstrom CE, Thiele EA, Turner Z, Vaccarezza MM, van der Louw EJTM, Veggiotti P, Wheless JW, Wirrell EC; Charlie Foundation; Matthew's Friends; Practice Committee of the Child Neurology Society. Kossoff EH, et al. Among authors: kang hc. Epilepsia Open. 2018 May 21;3(2):175-192. doi: 10.1002/epi4.12225. eCollection 2018 Jun. Epilepsia Open. 2018. PMID: 29881797 Free PMC article.
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene.
Barba C, Blumcke I, Winawer MR, Hartlieb T, Kang HC, Grisotto L, Chipaux M, Bien CG, Heřmanovská B, Porter BE, Lidov HGW, Cetica V, Woermann FG, Lopez-Rivera JA, Canoll PD, Mader I, D'Incerti L, Baldassari S, Yang E, Gaballa A, Vogel H, Straka B, Macconi L, Polster T, Grant GA, Krsková L, Shin HJ, Ko A, Crino PB, Krsek P, Lee JH, Lal D, Baulac S, Poduri A, Guerrini R; SLC35A2 Study Group. Barba C, et al. Among authors: kang hc. Neurology. 2023 Jan 31;100(5):e528-e542. doi: 10.1212/WNL.0000000000201471. Epub 2022 Oct 28. Neurology. 2023. PMID: 36307217 Free PMC article.
Genotypes and phenotypes of DNM1 encephalopathy.
Kim J, Teng LY, Shaker B, Na D, Koh HY, Kwon SS, Lee JS, Kim HD, Kang HC, Kim SH. Kim J, et al. Among authors: kang hc. J Med Genet. 2023 Nov;60(11):1076-1083. doi: 10.1136/jmg-2023-109233. Epub 2023 May 29. J Med Genet. 2023. PMID: 37248033
Mitochondrial disease and epilepsy.
Kang HC, Lee YM, Kim HD. Kang HC, et al. Brain Dev. 2013 Sep;35(8):757-61. doi: 10.1016/j.braindev.2013.01.006. Epub 2013 Feb 13. Brain Dev. 2013. PMID: 23414619 Review.
Clinical characteristics of KCNQ2 encephalopathy.
Kim HJ, Yang D, Kim SH, Won D, Kim HD, Lee JS, Choi JR, Lee ST, Kang HC. Kim HJ, et al. Among authors: kang hc. Brain Dev. 2021 Feb;43(2):244-250. doi: 10.1016/j.braindev.2020.08.015. Epub 2020 Sep 8. Brain Dev. 2021. PMID: 32917465
Acute Necrotizing Myelitis Associated with COVID-19.
Yoo JE, Shin HJ, Kang HC, Lee JS, Kim HD, Lee HN. Yoo JE, et al. Among authors: kang hc. Yonsei Med J. 2023 Nov;64(11):692-695. doi: 10.3349/ymj.2023.0202. Yonsei Med J. 2023. PMID: 37880851 Free PMC article.
Analysis of trio test in neurodevelopmental disorders.
Kim SH, Kwon SS, Lee JS, Kim HD, Lee ST, Choi JR, Shin S, Kang HC. Kim SH, et al. Among authors: kang hc. Front Pediatr. 2022 Dec 23;10:1073083. doi: 10.3389/fped.2022.1073083. eCollection 2022. Front Pediatr. 2022. PMID: 36619507 Free PMC article.
187 results