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FARS2 mutation and epilepsy: Possible link with early-onset epileptic encephalopathy.
Cho JS, Kim SH, Kim HY, Chung T, Kim D, Jang S, Lee SB, Yoo SK, Shin J, Kim JI, Kim H, Hwang H, Chae JH, Choi J, Kim KJ, Lim BC. Cho JS, et al. Among authors: kim ji, kim kj, kim hy, kim h, kim sh, kim d. Epilepsy Res. 2017 Jan;129:118-124. doi: 10.1016/j.eplepsyres.2016.11.022. Epub 2016 Dec 2. Epilepsy Res. 2017. PMID: 28043061 Review.
Childhood ocular myasthenia gravis.
Kim JH, Hwang JM, Hwang YS, Kim KJ, Chae J. Kim JH, et al. Among authors: kim kj. Ophthalmology. 2003 Jul;110(7):1458-62. doi: 10.1016/S0161-6420(03)00460-3. Ophthalmology. 2003. PMID: 12867410
Clinical features of A3243G mitochondrial tRNA mutation.
Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ. Chae JH, et al. Among authors: kim kj. Brain Dev. 2004 Oct;26(7):459-62. doi: 10.1016/j.braindev.2004.01.002. Brain Dev. 2004. PMID: 15351082
New antiepileptic drugs in pediatric epilepsy.
Hwang H, Kim KJ. Hwang H, et al. Among authors: kim kj. Brain Dev. 2008 Oct;30(9):549-55. doi: 10.1016/j.braindev.2008.01.007. Epub 2008 Mar 6. Brain Dev. 2008. PMID: 18328657
Merosin-deficient congenital muscular dystrophy in Korea.
Chae JH, Lee JS, Hwang H, Kim KJ, Hwang YS, Park JD, Cheon JE, Kim IO, Choe GY, Park SH. Chae JH, et al. Among authors: kim kj, kim io. Brain Dev. 2009 May;31(5):341-6. doi: 10.1016/j.braindev.2008.06.009. Epub 2008 Aug 23. Brain Dev. 2009. PMID: 18723302
3,035 results