Hong YB - Search Results

1

A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement.

Park JM, Kim YJ, Yoo JH, Hong YB, Park JH, Koo H, Chung KW, Choi BO. Park JM, et al. Among authors: hong yb. Neuromuscul Disord. 2013 Jul;23(7):580-6. doi: 10.1016/j.nmd.2013.04.003. Epub 2013 May 24. Neuromuscul Disord. 2013. PMID: 23707328

2

Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.

Lee SS, Lee HJ, Park JM, Hong YB, Park KD, Yoo JH, Koo H, Jung SC, Park HS, Lee JH, Lee MG, Hyun YS, Nakhro K, Chung KW, Choi BO. Lee SS, et al. Among authors: hong yb. JAMA Neurol. 2013 May;70(5):607-15. doi: 10.1001/jamaneurol.2013.1250. JAMA Neurol. 2013. PMID: 23553329

3

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: hong yb. Neurology. 2013 Jul 9;81(2):165-73. doi: 10.1212/WNL.0b013e31829a3421. Epub 2013 Jun 7. Neurology. 2013. PMID: 23749797

4

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease.

Kim HJ, Hong YB, Park JM, Choi YR, Kim YJ, Yoon BR, Koo H, Yoo JH, Kim SB, Park M, Chung KW, Choi BO. Kim HJ, et al. Among authors: hong yb. Orphanet J Rare Dis. 2013 Jul 12;8:104. doi: 10.1186/1750-1172-8-104. Orphanet J Rare Dis. 2013. PMID: 23844677 Free PMC article.

5

Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.

Suh BC, Hong YB, Nakhro K, Nam SH, Chung KW, Choi BO. Suh BC, et al. Among authors: hong yb. Mol Med Rep. 2014 Feb;9(2):481-6. doi: 10.3892/mmr.2013.1808. Epub 2013 Nov 18. Mol Med Rep. 2014. PMID: 24247255

6

Exome Sequencing Reveals a Novel PRPS1 Mutation in a Family with CMTX5 without Optic Atrophy.

Park J, Hyun YS, Kim YJ, Nam SH, Kim SH, Hong YB, Park JM, Chung KW, Choi BO. Park J, et al. Among authors: hong yb. J Clin Neurol. 2013 Oct;9(4):283-8. doi: 10.3988/jcn.2013.9.4.283. Epub 2013 Oct 31. J Clin Neurol. 2013. PMID: 24285972 Free PMC article.

7

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease.

Hong YB, Lee JH, Park JM, Choi YR, Hyun YS, Yoon BR, Yoo JH, Koo H, Jung SC, Chung KW, Choi BO. Hong YB, et al. BMC Med Genet. 2013 Dec 5;14:125. doi: 10.1186/1471-2350-14-125. BMC Med Genet. 2013. PMID: 24314034 Free PMC article.

8

Proximal lower-limb weakness in Charcot-Marie-Tooth disease-reply.

Chung KW, Lee SS, Hong YB, Yoo JH, Choi BO. Chung KW, et al. Among authors: hong yb. JAMA Neurol. 2013 Dec;70(12):1587-8. doi: 10.1001/jamaneurol.2013.4770. JAMA Neurol. 2013. PMID: 24322517 No abstract available.

9

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy.

Park MH, Woo HM, Hong YB, Park JH, Yoon BR, Park JM, Yoo JH, Koo H, Chae JH, Chung KW, Choi BO, Koo SK. Park MH, et al. Among authors: hong yb. Neurogenetics. 2014 Aug;15(3):171-82. doi: 10.1007/s10048-014-0405-1. Epub 2014 May 10. Neurogenetics. 2014. PMID: 24816431 Free PMC article.

10

Dynamic transcriptional events in distal sural nerve revealed by transcriptome analysis.

Hong YB, Jung SC, Lee J, Moon HS, Chung KW, Choi BO. Hong YB, et al. Exp Neurobiol. 2014 Jun;23(2):169-72. doi: 10.5607/en.2014.23.2.169. Epub 2014 Jun 13. Exp Neurobiol. 2014. PMID: 24963282 Free PMC article.

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