Lim BC - Search Results

1

FARS2 mutation and epilepsy: Possible link with early-onset epileptic encephalopathy.

Cho JS, Kim SH, Kim HY, Chung T, Kim D, Jang S, Lee SB, Yoo SK, Shin J, Kim JI, Kim H, Hwang H, Chae JH, Choi J, Kim KJ, Lim BC. Cho JS, et al. Among authors: lim bc. Epilepsy Res. 2017 Jan;129:118-124. doi: 10.1016/j.eplepsyres.2016.11.022. Epub 2016 Dec 2. Epilepsy Res. 2017. PMID: 28043061 Review.

2

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: lim bc. Brain Dev. 2004 Oct;26(7):459-62. doi: 10.1016/j.braindev.2004.01.002. Brain Dev. 2004. PMID: 15351082

3

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

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: lim bc. J Child Neurol. 2010 Jun;25(6):728-31. doi: 10.1177/0883073809342273. Epub 2009 Sep 22. J Child Neurol. 2010. PMID: 19773463

5

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: lim bc. J Child Neurol. 2010 Aug;25(8):1047-50. doi: 10.1177/0883073809356710. Epub 2010 Jan 27. J Child Neurol. 2010. PMID: 20110213

6

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: lim bc. 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

7

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. J Child Neurol. 2010 Apr;25(4):490-3. doi: 10.1177/0883073809357937. J Child Neurol. 2010. PMID: 20382953

8

A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with Danon disease.

Kim H, Cho A, Lim BC, Kim MJ, Kim KJ, Nishino I, Hwang YS, Chae JH. Kim H, et al. Among authors: lim bc. Muscle Nerve. 2010 Jun;41(6):879-82. doi: 10.1002/mus.21614. Muscle Nerve. 2010. PMID: 20513107

9

Clinical presentations and neurodevelopmental outcomes of perinatal stroke in preterm and term neonates: a case series.

Lee HJ, Lim BC, Hwang H, Hong JS, Kim EK, Kim HS, Kim BI, Choi JH, Choi CW. Lee HJ, et al. Among authors: lim bc. J Korean Med Sci. 2010 Jun;25(6):888-94. doi: 10.3346/jkms.2010.25.6.888. Epub 2010 May 24. J Korean Med Sci. 2010. PMID: 20514310 Free PMC article.

10

Glutaric aciduria type 1 in Korea: report of two novel mutations.

Park JD, Lim B, Kim KJ, Hwang YS, Kim SK, Kang SH, Cho SI, Park SS, Lee JS, Chae JH. Park JD, et al. J Korean Med Sci. 2010 Jun;25(6):957-60. doi: 10.3346/jkms.2010.25.6.957. Epub 2010 May 24. J Korean Med Sci. 2010. PMID: 20514322 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

235 results

Search Page