Choi KG - Search Results

1

Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients.

Choi BO, Lee MS, Shin SH, Hwang JH, Choi KG, Kim WK, Sunwoo IN, Kim NK, Chung KW. Choi BO, et al. Among authors: choi kg. Hum Mutat. 2004 Aug;24(2):185-6. doi: 10.1002/humu.9261. Hum Mutat. 2004. PMID: 15241803

2

A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease.

Chung KW, Kim SM, Sunwoo IN, Cho SY, Hwang SJ, Kim J, Kang SH, Park KD, Choi KG, Choi IS, Choi BO. Chung KW, et al. Among authors: choi kg, choi bo, choi is. J Hum Genet. 2008;53(4):360-364. doi: 10.1007/s10038-008-0249-3. Epub 2008 Jan 31. J Hum Genet. 2008. PMID: 18231710

3

MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis.

Choi BO, Kim SB, Kanwal S, Hyun YS, Park SW, Koo H, Yoo JH, Hyun JW, Park KD, Choi KG, Chung KW. Choi BO, et al. Among authors: choi kg. Int J Mol Med. 2011 Sep;28(3):389-96. doi: 10.3892/ijmm.2011.678. Epub 2011 Apr 18. Int J Mol Med. 2011. PMID: 21503568

4

Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.

Choi BO, Koo SK, Park MH, Rhee H, Yang SJ, Choi KG, Jung SC, Kim HS, Hyun YS, Nakhro K, Lee HJ, Woo HM, Chung KW. Choi BO, et al. Among authors: choi kg. Hum Mutat. 2012 Nov;33(11):1610-5. doi: 10.1002/humu.22143. Epub 2012 Jul 5. Hum Mutat. 2012. PMID: 22730194

5

A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.

Choi BO, Kang SH, Hyun YS, Kanwal S, Park SW, Koo H, Kim SB, Choi YC, Yoo JH, Kim JW, Park KD, Choi KG, Kim SJ, Züchner S, Chung KW. Choi BO, et al. Among authors: choi kg, choi yc. Hum Mutat. 2011 Jun;32(6):669-77. doi: 10.1002/humu.21488. Epub 2011 Apr 7. Hum Mutat. 2011. PMID: 21480433 Free PMC article.

6

Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.

Kim YH, Chung HK, Park KD, Choi KG, Kim SM, Sunwoo IN, Choi YC, Lim JG, Lee KW, Kim KK, Lee DK, Joo IS, Kwon KH, Gwon SB, Park JH, Kim DS, Kim SH, Kim WK, Suh BC, Kim SB, Kim NH, Sohn EH, Kim OJ, Kim HS, Cho JH, Kang SY, Park CI, Oh J, Shin JH, Chung KW, Choi BO. Kim YH, et al. Among authors: choi kg, choi bo, choi yc. J Clin Neurol. 2012 Jun;8(2):139-45. doi: 10.3988/jcn.2012.8.2.139. Epub 2012 Jun 29. J Clin Neurol. 2012. PMID: 22787498 Free PMC article.

7

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.

Nakhro K, Park JM, Hong YB, Park JH, Nam SH, Yoon BR, Yoo JH, Koo H, Jung SC, Kim HL, Kim JY, Choi KG, Choi BO, Chung KW. Nakhro K, et al. Among authors: choi kg, choi bo. Neurology. 2013 Jul 9;81(2):165-73. doi: 10.1212/WNL.0b013e31829a3421. Epub 2013 Jun 7. Neurology. 2013. PMID: 23749797

8

Motor cortical excitability in patients with poststroke epilepsy.

Kim JH, Lee HW, Cohen LG, Park KD, Choi KG. Kim JH, et al. Among authors: choi kg. Epilepsia. 2008 Jan;49(1):117-24. doi: 10.1111/j.1528-1167.2007.01231.x. Epub 2007 Aug 2. Epilepsia. 2008. PMID: 17672852 Free article.

9

A survey of sleep deprivation patterns and their effects on cognitive functions of residents and interns in Korea.

Kim HJ, Kim JH, Park KD, Choi KG, Lee HW. Kim HJ, et al. Among authors: choi kg. Sleep Med. 2011 Apr;12(4):390-6. doi: 10.1016/j.sleep.2010.09.010. Sleep Med. 2011. PMID: 21388879

10

A 6-month longitudinal study of bone mineral density with antiepileptic drug monotherapy.

Kim SH, Lee JW, Choi KG, Chung HW, Lee HW. Kim SH, et al. Among authors: choi kg. Epilepsy Behav. 2007 Mar;10(2):291-5. doi: 10.1016/j.yebeh.2006.11.007. Epub 2007 Jan 16. Epilepsy Behav. 2007. PMID: 17224308

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