Hwang YS - Search Results

1

Comparison of flunarizine and topiramate for the prophylaxis of pediatric migraines.

Kim H, Byun SH, Kim JS, Lim BC, Chae JH, Choi J, Kim KJ, Hwang YS, Hwang H. Kim H, et al. Among authors: hwang h, hwang ys. Eur J Paediatr Neurol. 2013 Jan;17(1):45-9. doi: 10.1016/j.ejpn.2012.10.001. Epub 2012 Oct 27. Eur J Paediatr Neurol. 2013. PMID: 23111149

2

Lacosamide as an adjunctive therapy in pediatric patients with refractory focal epilepsy.

Kim JS, Kim H, Lim BC, Chae JH, Choi J, Kim KJ, Hwang YS, Hwang H. Kim JS, et al. Among authors: hwang h, hwang ys. Brain Dev. 2014 Jun;36(6):510-5. doi: 10.1016/j.braindev.2013.07.003. Epub 2013 Aug 12. Brain Dev. 2014. PMID: 23948372

3

Effectiveness of intravenous levetiracetam as an adjunctive treatment in pediatric refractory status epilepticus.

Kim JS, Lee JH, Ryu HW, Lim BC, Hwang H, Chae JH, Choi J, Kim KJ, Hwang YS, Kim H. Kim JS, et al. Among authors: hwang h, hwang ys. Pediatr Emerg Care. 2014 Aug;30(8):525-8. doi: 10.1097/PEC.0000000000000183. Pediatr Emerg Care. 2014. PMID: 25062293

4

Cerebellum can be a possible generator of progressive myoclonus.

Koh KN, Lim BC, Hwang H, Park JD, Chae JH, Kim KJ, Hwang YS, Kim SK, Wang KC, Moon HK. Koh KN, et al. Among authors: hwang h, hwang ys. J Child Neurol. 2010 Jun;25(6):728-31. doi: 10.1177/0883073809342273. Epub 2009 Sep 22. J Child Neurol. 2010. PMID: 19773463

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

6

Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism.

Kim SH, Hwang H, Chae JH, Kim KJ, Hwang YS, Lim BC. Kim SH, et al. Among authors: hwang h, hwang ys. J Child Neurol. 2010 Aug;25(8):1047-50. doi: 10.1177/0883073809356710. Epub 2010 Jan 27. J Child Neurol. 2010. PMID: 20110213

7

A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy.

Chae JH, Lim BC, Cheong HI, Hwang YS, Kim KJ, Hwang H. Chae JH, et al. Among authors: hwang h, hwang ys. J Neurol Sci. 2010 May 15;292(1-2):104-6. doi: 10.1016/j.jns.2010.02.006. Epub 2010 Mar 11. J Neurol Sci. 2010. PMID: 20226471

8

Andersen cardiodysrhythmic periodic paralysis with KCNJ2 mutations: a novel mutation in the pore selectivity filter residue.

Lim BC, Kim GB, Bae EJ, Noh CI, Hwang H, Kim KJ, Hwang YS, Ko TS, Chae JH. Lim BC, et al. Among authors: hwang h, hwang ys. J Child Neurol. 2010 Apr;25(4):490-3. doi: 10.1177/0883073809357937. J Child Neurol. 2010. PMID: 20382953

9

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: hwang ys. J Neurosurg Pediatr. 2010 Jul;6(1):49-56. doi: 10.3171/2010.3.PEDS09497. J Neurosurg Pediatr. 2010. PMID: 20593988

10

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: hwang h, hwang ys. Mult Scler. 2011 Jan;17(1):67-73. doi: 10.1177/1352458510382685. Epub 2010 Sep 21. Mult Scler. 2011. PMID: 20858690

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