Chae J - Search Results

1

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

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

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

4

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

5

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. 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

6

A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.

Chae JH, Lee JS, Kim KJ, Hwang YS, Bonilla E, Tanji K, Hirano M. Chae JH, et al. Pediatr Res. 2007 May;61(5 Pt 1):622-4. doi: 10.1203/pdr.0b013e3180459f2d. Pediatr Res. 2007. PMID: 17413873

7

Biochemical and genetic analysis of Leigh syndrome patients in Korea.

Chae JH, Lee JS, Kim KJ, Hwang YS, Hirano M. Chae JH, et al. Brain Dev. 2008 Jun;30(6):387-90. doi: 10.1016/j.braindev.2007.11.001. Epub 2007 Dec 21. Brain Dev. 2008. PMID: 18155376 Free PMC article.

8

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

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. J Child Neurol. 2009 Jul;24(7):828-32. doi: 10.1177/0883073808331085. J Child Neurol. 2009. PMID: 19617458

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