Park KJ - Search Results

1

Streptococcus suis meningitis with bilateral sensorineural hearing loss.

Huh HJ, Park KJ, Jang JH, Lee M, Lee JH, Ahn YH, Kang CI, Ki CS, Lee NY. Huh HJ, et al. Among authors: park kj. Korean J Lab Med. 2011 Jul;31(3):205-11. doi: 10.3343/kjlm.2011.31.3.205. Epub 2011 Jun 28. Korean J Lab Med. 2011. PMID: 21779197 Free PMC article.

2

Clinical, pharmacokinetic, and pharmacogenetic determinants of clopidogrel resistance in Korean patients with acute coronary syndrome.

Park KJ, Chung HS, Kim SR, Kim HJ, Han JY, Lee SY. Park KJ, et al. Korean J Lab Med. 2011 Apr;31(2):91-4. doi: 10.3343/kjlm.2011.31.2.91. Korean J Lab Med. 2011. PMID: 21474982 Free PMC article.

3

Evaluation of the diagnostic performance of fibrin monomer in disseminated intravascular coagulation.

Park KJ, Kwon EH, Kim HJ, Kim SH. Park KJ, et al. Korean J Lab Med. 2011 Jul;31(3):143-7. doi: 10.3343/kjlm.2011.31.3.143. Epub 2011 Jun 28. Korean J Lab Med. 2011. PMID: 21779185 Free PMC article.

4

A novel PHKA2 gross deletion mutation in a Korean patient with X-linked liver glycogenosis type I.

Park KJ, Park HD, Lee SY, Ki CS, Choe YH. Park KJ, et al. Among authors: park hd. Ann Clin Lab Sci. 2011 Spring;41(2):197-200. Ann Clin Lab Sci. 2011. PMID: 21844581

5

SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).

Kim HJ, Won HH, Park KJ, Hong SH, Ki CS, Cho SS, Venselaar H, Vriend G, Kim JW. Kim HJ, et al. Among authors: park kj. PLoS One. 2013 Nov 18;8(11):e79063. doi: 10.1371/journal.pone.0079063. eCollection 2013. PLoS One. 2013. PMID: 24260153 Free PMC article. Clinical Trial.

6

Clinical application of catalytically cleavable fluorescence probe technology for multiplexing quantification of BCR-ABL1 fusion transcripts.

Park KJ, Woo YM, Kim K, Lee ST, Ki CS, Kim HJ, Kim SH, Kim JW. Park KJ, et al. Clin Chim Acta. 2014 Jan 20;428:72-6. Clin Chim Acta. 2014. PMID: 24482808

7

Clinical Interpretation Challenges of Germline-Shared Somatic Variants in Cancer.

Park KJ. Park KJ. Lab Med. 2022 Jan 6;53(1):24-29. doi: 10.1093/labmed/lmab020. Lab Med. 2022. PMID: 34184037

8

DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.

Park KJ, Park HK, Kim YJ, Lee KR, Park JH, Park JH, Park HD, Lee SY, Kim JW. Park KJ, et al. Among authors: park jh, park hd, park hk. Ann Lab Med. 2016 Mar;36(2):145-53. doi: 10.3343/alm.2016.36.2.145. Ann Lab Med. 2016. PMID: 26709262 Free PMC article.

9

The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene.

Park KJ, Park JH, Park JH, Cho EB, Kim BJ, Kim JW. Park KJ, et al. Among authors: park jh. Ann Lab Med. 2016 May;36(3):259-62. doi: 10.3343/alm.2016.36.3.259. Ann Lab Med. 2016. PMID: 26915616 Free PMC article.

10

Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome.

Park KJ, Choi HJ, Suh SP, Ki CS, Kim JW. Park KJ, et al. Ann Lab Med. 2016 Sep;36(5):463-8. doi: 10.3343/alm.2016.36.5.463. Ann Lab Med. 2016. PMID: 27374712 Free PMC article.

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