Lee JD - Search Results

1

Genetic analysis of auditory neuropathy spectrum disorder in the Korean population.

Bae SH, Baek JI, Lee JD, Song MH, Kwon TJ, Oh SK, Jeong JY, Choi JY, Lee KY, Kim UK. Bae SH, et al. Among authors: lee jd, lee ky. Gene. 2013 Jun 10;522(1):65-9. doi: 10.1016/j.gene.2013.02.057. Epub 2013 Apr 4. Gene. 2013. PMID: 23562982

2

Management of facial nerve schwannoma in patients with favorable facial function.

Lee JD, Kim SH, Song MH, Lee HK, Lee WS. Lee JD, et al. Among authors: lee ws, lee hk. Laryngoscope. 2007 Jun;117(6):1063-8. doi: 10.1097/MLG.0b013e31804b1a51. Laryngoscope. 2007. PMID: 17464236

3

Jugular foramen schwannoma: analysis on its origin and location.

Song MH, Lee HY, Jeon JS, Lee JD, Lee HK, Lee WS. Song MH, et al. Among authors: lee jd, lee ws, lee hy, lee hk. Otol Neurotol. 2008 Apr;29(3):387-91. doi: 10.1097/MAO.0b013e318164cb83. Otol Neurotol. 2008. PMID: 18277311

4

A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.

Lee JD, Kim SC, Koh YW, Lee HJ, Choi SY, Kim UK. Lee JD, et al. Among authors: lee hj. Ann Clin Lab Sci. 2009 Summer;39(3):303-6. Ann Clin Lab Sci. 2009. PMID: 19667416

5

Genetic and epigenetic alterations of the NF2 gene in sporadic vestibular schwannomas.

Lee JD, Kwon TJ, Kim UK, Lee WS. Lee JD, et al. Among authors: lee ws. PLoS One. 2012;7(1):e30418. doi: 10.1371/journal.pone.0030418. Epub 2012 Jan 25. PLoS One. 2012. PMID: 22295085 Free PMC article.

6

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.

7

A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome.

Park MK, Sagong B, Lee JD, Bae SH, Lee B, Choi KS, Choo YS, Lee KY, Kim UK. Park MK, et al. Among authors: lee jd, lee ky, lee b. Int J Pediatr Otorhinolaryngol. 2014 Nov;78(11):1996-9. doi: 10.1016/j.ijporl.2014.08.009. Epub 2014 Aug 17. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25223473

8

Early deterioration of residual hearing in patients with SLC26A4 mutations.

Kim BG, Roh KJ, Park AY, Lee SC, Kang BS, Seo YJ, Lee JD, Choi JY. Kim BG, et al. Among authors: lee jd, lee sc. Laryngoscope. 2016 Aug;126(8):E286-91. doi: 10.1002/lary.25786. Epub 2015 Dec 9. Laryngoscope. 2016. PMID: 26650914

9

Analysis of Prognostic Factors in Malignant External Otitis.

Lee SK, Lee SA, Seon SW, Jung JH, Lee JD, Choi JY, Kim BG. Lee SK, et al. Among authors: lee jd, lee sa. Clin Exp Otorhinolaryngol. 2017 Sep;10(3):228-235. doi: 10.21053/ceo.2016.00612. Epub 2016 Sep 27. Clin Exp Otorhinolaryngol. 2017. PMID: 27671716 Free PMC article.

10

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report.

Choi HJ, Lee JS, Yu S, Cha DH, Gee HY, Choi JY, Lee JD, Jung J. Choi HJ, et al. Among authors: lee js, lee jd. BMC Med Genet. 2017 Dec 19;18(1):151. doi: 10.1186/s12881-017-0511-7. BMC Med Genet. 2017. PMID: 29258540 Free PMC article.

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