Chae JH - Search Results

1

Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia.

Choi SA, Kim SY, Kim H, Kim WJ, Kim H, Hwang H, Choi JE, Lim BC, Chae JH, Chong S, Lee JY, Phi JH, Kim SK, Wang KC, Kim KJ. Choi SA, et al. Among authors: chae jh. Epilepsy Res. 2018 Jan;139:54-59. doi: 10.1016/j.eplepsyres.2017.11.012. Epub 2017 Nov 27. Epilepsy Res. 2018. PMID: 29197666

2

Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome.

Chae JH, Hwang YS, Kim KJ. Chae JH, et al. J Child Neurol. 2002 Jan;17(1):33-6. doi: 10.1177/088307380201700108. J Child Neurol. 2002. PMID: 11913567

3

Childhood ocular myasthenia gravis.

Kim JH, Hwang JM, Hwang YS, Kim KJ, Chae J. Kim JH, et al. Among authors: chae j. Ophthalmology. 2003 Jul;110(7):1458-62. doi: 10.1016/S0161-6420(03)00460-3. Ophthalmology. 2003. PMID: 12867410

4

Clinical features of A3243G mitochondrial tRNA mutation.

Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ. Chae JH, et al. Brain Dev. 2004 Oct;26(7):459-62. doi: 10.1016/j.braindev.2004.01.002. Brain Dev. 2004. PMID: 15351082

5

Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotype.

Chae JH, Hwang H, Hwang YS, Cheong HJ, Kim KJ. Chae JH, et al. J Child Neurol. 2004 Jul;19(7):503-8. doi: 10.1177/08830738040190070501. J Child Neurol. 2004. PMID: 15526954

6

Surgical outcome and prognostic factors of pediatric epilepsy caused by cortical dysplasia.

Park CK, Kim SK, Wang KC, Hwang YS, Kim KJ, Chae JH, Chi JG, Choe GY, Kim NR, Cho BK. Park CK, et al. Among authors: chae jh. Childs Nerv Syst. 2006 Jun;22(6):586-92. doi: 10.1007/s00381-006-0085-8. Epub 2006 Mar 16. Childs Nerv Syst. 2006. PMID: 16541293

7

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: chae jh. J Neurosurg Pediatr. 2008 Apr;1(4):277-83. doi: 10.3171/PED/2008/1/4/277. J Neurosurg Pediatr. 2008. PMID: 18377302

8

Congenital subependymal giant cell astrocytoma: clinical considerations and expression of radial glial cell markers in giant cells.

Phi JH, Park SH, Chae JH, Hong KH, Park SS, Kang JH, Jun JK, Cho BK, Wang KC, Kim SK. Phi JH, et al. Among authors: chae jh. Childs Nerv Syst. 2008 Dec;24(12):1499-503. doi: 10.1007/s00381-008-0681-x. Epub 2008 Jul 16. Childs Nerv Syst. 2008. PMID: 18629509

9

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. 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

10

Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies.

Lim BC, Park JD, Hwang H, Kim KJ, Hwang YS, Chae JH, Cheon JE, Kim IO, Lee R, Moon HK. Lim BC, et al. Among authors: chae jh. J Child Neurol. 2009 Jul;24(7):828-32. doi: 10.1177/0883073808331085. J Child Neurol. 2009. PMID: 19617458

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