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A novel double mutation in cis in MFN2 causes Charcot-Marie-Tooth neuropathy type 2A.

Park SY, Kim SY, Hong YH, Cho SI, Seong MW, Park SS. Park SY, et al. Among authors: hong yh. Neurogenetics. 2012 Aug;13(3):275-80. doi: 10.1007/s10048-012-0327-8. Epub 2012 Apr 20. Neurogenetics. 2012. PMID: 22526351

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Novel compound heterozygous mutations of the SPG11 gene in Korean families with hereditary spastic paraplegia with thin corpus callosum.

Kim SM, Lee JS, Kim S, Kim HJ, Kim MH, Lee KM, Hong YH, Park KS, Sung JJ, Lee KW. Kim SM, et al. Among authors: hong yh. J Neurol. 2009 Oct;256(10):1714-8. doi: 10.1007/s00415-009-5189-0. Epub 2009 Jun 10. J Neurol. 2009. PMID: 19513778

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A novel splicing mutation (c.870+3A>G) in SPG4 in a Korean family with hereditary spastic paraplegia.

Lim JS, Sung JJ, Hong YH, Park SS, Park KS, Cha JI, Lee JY, Lee KW. Lim JS, et al. Among authors: hong yh. J Neurol Sci. 2010 Mar 15;290(1-2):186-9. doi: 10.1016/j.jns.2009.10.016. Epub 2009 Nov 25. J Neurol Sci. 2010. PMID: 19939411

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Axonal conduction block at intermediate nerve segments in pure motor Guillain-Barré syndrome.

Hong YH, Sung JJ, Oh MY, Moon HJ, Park KS, Lee KW. Hong YH, et al. J Peripher Nerv Syst. 2011 Mar;16(1):37-46. doi: 10.1111/j.1529-8027.2011.00314.x. J Peripher Nerv Syst. 2011. PMID: 21504501

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Ischemic neuropathy associated with livedoid vasculitis.

Kim JE, Park SY, Sinn DI, Kim SM, Hong YH, Park KS, Sung JJ, Lee KW. Kim JE, et al. Among authors: hong yh. J Clin Neurol. 2011 Dec;7(4):233-6. doi: 10.3988/jcn.2011.7.4.233. Epub 2011 Dec 29. J Clin Neurol. 2011. PMID: 22259622 Free PMC article.

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Comparison of MOG and AQP4 antibody seroprevalence in Korean adults with inflammatory demyelinating CNS diseases.

Hyun JW, Lee HL, Jeong WK, Lee HJ, Shin JH, Min JH, Kim BJ, Kim SW, Shin HY, Oh J, Kim W, Shin HJ, Oh SY, Kim H, Lim YM, Huh SY, Cho EB, Nam TS, Lee SH, Kim SY, Kang SY, Han SG, Sohn EH, Baek SH, Kim BJ, Lee SS, Seok JM, Hong YH, Oh SI, Kim JK, Shin KJ, Kwon O, Cho JY, Bae JS, Kim SY, Kim Y, Lee MY, Kim SH, Kim HJ. Hyun JW, et al. Among authors: hong yh. Mult Scler. 2021 May;27(6):964-967. doi: 10.1177/1352458520948213. Epub 2020 Aug 11. Mult Scler. 2021. PMID: 32779521

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Autosomal dominant centronuclear myopathy with unique clinical presentations.

Lee JY, Min JH, Hong YH, Sung JJ, Park SH, Park SH, Lee KW, Park KS. Lee JY, et al. Among authors: hong yh. J Korean Med Sci. 2007 Dec;22(6):1098-101. doi: 10.3346/jkms.2007.22.6.1098. J Korean Med Sci. 2007. PMID: 18162732 Free PMC article.

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Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.

Ki CS, Lee ST, Kim KS, Kim JW, Hong YH, Sung JJ, Park KS, Lee KW. Ki CS, et al. Among authors: hong yh. J Korean Med Sci. 2008 Dec;23(6):959-63. doi: 10.3346/jkms.2008.23.6.959. Epub 2008 Dec 23. J Korean Med Sci. 2008. PMID: 19119436 Free PMC article.

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Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.

Kim SY, Kim JY, Kim GP, Sung JJ, Lim KS, Lee KW, Chae JH, Hong YH, Seong MW, Park SS. Kim SY, et al. Among authors: hong yh. Korean J Lab Med. 2008 Dec;28(6):483-92. doi: 10.3343/kjlm.2008.28.6.483. Korean J Lab Med. 2008. PMID: 19127114

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Up-regulation of the receptor for advanced glycation end products in the skin biopsy specimens of patients with severe diabetic neuropathy.

Park SY, Kim YA, Hong YH, Moon MK, Koo BK, Kim TW. Park SY, et al. Among authors: hong yh. J Clin Neurol. 2014 Oct;10(4):334-41. doi: 10.3988/jcn.2014.10.4.334. Epub 2014 Oct 6. J Clin Neurol. 2014. PMID: 25324883 Free PMC article.

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