Kwon SS - Search Results

1

Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing.

Rim JH, Kim SH, Hwang IS, Kwon SS, Kim J, Kim HW, Cho MJ, Ko A, Youn SE, Kim J, Lee YM, Chung HJ, Lee JS, Kim HD, Choi JR, Lee ST, Kang HC. Rim JH, et al. Among authors: kwon ss. BMC Med Genomics. 2018 Feb 1;11(1):6. doi: 10.1186/s12920-018-0320-7. BMC Med Genomics. 2018. PMID: 29390993 Free PMC article.

2

New ORP/pH based control strategy for chlorination and dechlorination of wastewater: pilot scale application.

Kim H, Kwon S, Han S, Yu M, Kim J, Gong S, Colosimo MF. Kim H, et al. Water Sci Technol. 2006;53(6):145-51. doi: 10.2166/wst.2006.188. Water Sci Technol. 2006. PMID: 16749451

3

Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development.

Kwon SS, Kim J, Shin S, Lee ST, Lee KA, Choi JR. Kwon SS, et al. Ann Lab Med. 2018 Jan;38(1):77-79. doi: 10.3343/alm.2018.38.1.77. Ann Lab Med. 2018. PMID: 29071826 Free PMC article. No abstract available.

4

Efficacy of Stiripentol in Dravet Syndrome with or without SCN1A Mutations.

Cho MJ, Kwon SS, Ko A, Lee ST, Lee YM, Kim HD, Chung HJ, Kim SH, Lee JS, Kim DS, Kang HC. Cho MJ, et al. Among authors: kwon ss. J Clin Neurol. 2018 Jan;14(1):22-28. doi: 10.3988/jcn.2018.14.1.22. Epub 2017 Oct 31. J Clin Neurol. 2018. PMID: 29141279 Free PMC article.

5

Analysis of trio test in neurodevelopmental disorders.

Kim SH, Kwon SS, Lee JS, Kim HD, Lee ST, Choi JR, Shin S, Kang HC. Kim SH, et al. Among authors: kwon ss. Front Pediatr. 2022 Dec 23;10:1073083. doi: 10.3389/fped.2022.1073083. eCollection 2022. Front Pediatr. 2022. PMID: 36619507 Free PMC article.

6

Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders.

Kim SH, Kwon SS, Park MR, Lee HA, Kim JH, Cha J, Kim S, Baek ST, Kim SH, Lee JS, Kim HD, Choi JR, Lee ST, Kang HC. Kim SH, et al. Among authors: kwon ss. J Mol Diagn. 2023 Aug;25(8):583-591. doi: 10.1016/j.jmoldx.2023.04.003. Epub 2023 Apr 22. J Mol Diagn. 2023. PMID: 37088138 Free article.

7

Genotypes and phenotypes of DNM1 encephalopathy.

Kim J, Teng LY, Shaker B, Na D, Koh HY, Kwon SS, Lee JS, Kim HD, Kang HC, Kim SH. Kim J, et al. Among authors: kwon ss. J Med Genet. 2023 Nov;60(11):1076-1083. doi: 10.1136/jmg-2023-109233. Epub 2023 May 29. J Med Genet. 2023. PMID: 37248033

8

Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.

Kwon SS, Cho YK, Hahn S, Oh J, Won D, Shin S, Kang JM, Ahn JG, Lee ST, Choi JR. Kwon SS, et al. Front Immunol. 2023 May 31;14:1178582. doi: 10.3389/fimmu.2023.1178582. eCollection 2023. Front Immunol. 2023. PMID: 37325673 Free PMC article.

9

Corrigendum: Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.

Kwon SS, Cho YK, Hahn S, Oh J, Won D, Shin S, Kang JM, Ahn JG, Lee ST, Choi JR. Kwon SS, et al. Front Immunol. 2023 Jun 19;14:1235318. doi: 10.3389/fimmu.2023.1235318. eCollection 2023. Front Immunol. 2023. PMID: 37404832 Free PMC article.

10

Clinical relevance of clonal hematopoiesis and its interference in cell-free DNA profiling of patients with gastric cancer.

Lee KS, Lee CK, Kwon SS, Kwon WS, Park S, Lee ST, Choi JR, Rha SY, Shin S. Lee KS, et al. Among authors: kwon ws, kwon ss. Clin Chem Lab Med. 2023 Jul 13;62(1):178-186. doi: 10.1515/cclm-2023-0261. Print 2024 Jan 26. Clin Chem Lab Med. 2023. PMID: 37435889

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