Lee KY - Search Results

1

Novel EYA1 mutation in a Korean branchio-oto-renal syndrome family.

Lee KY, Kim S, Kim UK, Ki CS, Lee SH. Lee KY, et al. Among authors: lee sh. Int J Pediatr Otorhinolaryngol. 2007 Jan;71(1):169-74. doi: 10.1016/j.ijporl.2006.08.023. Epub 2006 Oct 17. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17049623

2

Novel therapy for hearing loss: delivery of insulin-like growth factor 1 to the cochlea using gelatin hydrogel.

Lee KY, Nakagawa T, Okano T, Hori R, Ono K, Tabata Y, Lee SH, Ito J. Lee KY, et al. Among authors: lee sh. Otol Neurotol. 2007 Oct;28(7):976-81. doi: 10.1097/MAO.0b013e31811f40db. Otol Neurotol. 2007. PMID: 17704706

3

Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss.

Bae JW, Lee KY, Choi SY, Lee SH, Park HJ, Kim UK. Bae JW, et al. Among authors: lee sh, lee ky. Int J Mol Med. 2008 Aug;22(2):175-80. Int J Mol Med. 2008. PMID: 18636170

4

Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss.

Choi SY, Park HJ, Lee KY, Dinh EH, Chang Q, Ahmad S, Lee SH, Bok J, Lin X, Kim UK. Choi SY, et al. Among authors: lee sh, lee ky. Hum Mutat. 2009 Jul;30(7):E716-27. doi: 10.1002/humu.21036. Hum Mutat. 2009. PMID: 19384972

5

A Family of H723R Mutation for SLC26A4 Associated with Enlarged Vestibular Aqueduct Syndrome.

Kim S, Song DG, Bae JW, Choi SY, Kim UK, Choi YJ, Lee KY, Lee SH, Lee JR. Kim S, et al. Among authors: lee sh, lee jr, lee ky. Clin Exp Otorhinolaryngol. 2009 Jun;2(2):100-2. doi: 10.3342/ceo.2009.2.2.100. Epub 2009 Jun 29. Clin Exp Otorhinolaryngol. 2009. PMID: 19565036 Free PMC article.

6

A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.

Lee HK, Park HJ, Lee KY, Park R, Kim UK. Lee HK, et al. Among authors: lee ky. Biochem Biophys Res Commun. 2010 Jun 4;396(3):626-30. doi: 10.1016/j.bbrc.2010.04.132. Epub 2010 Apr 29. Biochem Biophys Res Commun. 2010. PMID: 20434433

7

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

Sagong B, Park R, Kim YH, Lee KY, Baek JI, Cho HJ, Cho IJ, Kim UK, Lee SH. Sagong B, et al. Among authors: lee sh, lee ky. Ann Clin Lab Sci. 2010 Fall;40(4):380-5. Ann Clin Lab Sci. 2010. PMID: 20947814

8

Reversible Sensorineural Hearing Loss due to Pachymeningitis Associated with Elevated Serum MPO-ANCA.

Lim EJ, Kim SH, Lee SH, Lee KY, Choi JH, Nam EJ, Lee SH. Lim EJ, et al. Among authors: lee sh, lee ky. Clin Exp Otorhinolaryngol. 2011 Sep;4(3):155-8. doi: 10.3342/ceo.2011.4.3.155. Epub 2011 Feb 7. Clin Exp Otorhinolaryngol. 2011. PMID: 21949583 Free PMC article.

9

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY. Bae JW, et al. Among authors: lee sh, lee jd, lee ky. PLoS One. 2012;7(8):e42463. doi: 10.1371/journal.pone.0042463. Epub 2012 Aug 6. PLoS One. 2012. PMID: 22879993 Free PMC article.

10

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

Sagong B, Seok JH, Kwon TJ, Kim UK, Lee SH, Lee KY. Sagong B, et al. Among authors: lee sh, lee ky. Gene. 2012 Oct 15;508(1):135-9. doi: 10.1016/j.gene.2012.07.033. Epub 2012 Aug 4. Gene. 2012. PMID: 22884721

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