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Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center.
Cho A, Seong MW, Lim BC, Lee HJ, Byeon JH, Kim SS, Kim SY, Choi SA, Wong AL, Lee J, Kim JS, Ryu HW, Lee JS, Kim H, Hwang H, Choi JE, Kim KJ, Hwang YS, Hong KH, Park S, Cho SI, Lee SJ, Park H, Seo SH, Park SS, Chae JH. Cho A, et al. Among authors: kim kj, kim ss, kim h, kim sy, kim js. Muscle Nerve. 2017 May;55(5):727-734. doi: 10.1002/mus.25396. Epub 2017 Jan 20. Muscle Nerve. 2017. PMID: 27593222
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
Epilepsy surgery in children: outcomes and complications.
Kim SK, Wang KC, Hwang YS, Kim KJ, Chae JH, Kim IO, Cho BK. Kim SK, et al. Among authors: kim kj, kim io. J Neurosurg Pediatr. 2008 Apr;1(4):277-83. doi: 10.3171/PED/2008/1/4/277. J Neurosurg Pediatr. 2008. PMID: 18377302
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
3,034 results