Kim IO - Search Results

1

Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in Korea.

Lim BC, Ki CS, Kim JW, Cho A, Kim MJ, Hwang H, Kim KJ, Hwang YS, Park WY, Lim YJ, Kim IO, Lee JS, Chae JH. Lim BC, et al. Among authors: kim kj, kim io, kim jw, kim mj. Neuromuscul Disord. 2010 Aug;20(8):524-30. doi: 10.1016/j.nmd.2010.06.005. Neuromuscul Disord. 2010. PMID: 20620061

2

Leukodystrophy in children: a pictorial review of MR imaging features.

Cheon JE, Kim IO, Hwang YS, Kim KJ, Wang KC, Cho BK, Chi JG, Kim CJ, Kim WS, Yeon KM. Cheon JE, et al. Among authors: kim kj, kim io, kim cj, kim ws. Radiographics. 2002 May-Jun;22(3):461-76. doi: 10.1148/radiographics.22.3.g02ma01461. Radiographics. 2002. PMID: 12006681 Review.

3

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

4

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

5

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

6

Clinical and imaging findings of systemic hyalinosis: two cases presenting with congenital arthrogryposis.

Yoo SY, Kim JH, Kang HS, Hwang YS, Kim KJ, Kim IO, Cheon JE, Shin SM, Kim CJ, Lee JH, Lee MH, Chae JH. Yoo SY, et al. Among authors: kim kj, kim io, kim cj, kim jh. Skeletal Radiol. 2010 Jun;39(6):589-93. doi: 10.1007/s00256-009-0871-y. Epub 2010 Feb 6. Skeletal Radiol. 2010. PMID: 20140429

7

Pediatric moyamoya disease: An analysis of 410 consecutive cases.

Kim SK, Cho BK, Phi JH, Lee JY, Chae JH, Kim KJ, Hwang YS, Kim IO, Lee DS, Lee J, Wang KC. Kim SK, et al. Among authors: kim kj, kim io. Ann Neurol. 2010 Jul;68(1):92-101. doi: 10.1002/ana.21981. Ann Neurol. 2010. PMID: 20582955

8

Longitudinal analyses of the surgical outcomes of pediatric epilepsy patients with focal cortical dysplasia.

Phi JH, Cho BK, Wang KC, Lee JY, Hwang YS, Kim KJ, Chae JH, Kim IO, Park SH, Kim SK. Phi JH, et al. Among authors: kim kj, kim io, kim sk. J Neurosurg Pediatr. 2010 Jul;6(1):49-56. doi: 10.3171/2010.3.PEDS09497. J Neurosurg Pediatr. 2010. PMID: 20593988

9

Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica.

Lim BC, Hwang H, Kim KJ, Hwang YS, Cheon JE, Kim IO, Kim HJ, Chae JH. Lim BC, et al. Among authors: kim kj, kim hj, kim io. Mult Scler. 2011 Jan;17(1):67-73. doi: 10.1177/1352458510382685. Epub 2010 Sep 21. Mult Scler. 2011. PMID: 20858690

10

Sonographic features of sinus pericranii in 4 pediatric patients.

Kim YJ, Kim IO, Cheon JE, Lim YJ, Kim WS, Yeon KM. Kim YJ, et al. Among authors: kim io, kim ws. J Ultrasound Med. 2011 Mar;30(3):411-7. doi: 10.7863/jum.2011.30.3.411. J Ultrasound Med. 2011. PMID: 21357565

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