Muhwan Kim - Search Results

Year	Number of Results
2002	1
2003	1
2005	5
2006	4
2007	4
2008	8
2009	6
2010	9
2011	16
2012	10
2013	13
2014	11
2015	20
2016	16
2017	7
2018	11
2019	7
2020	11
2021	8
2022	6
2023	7
2024	4

1

Park HI, Kim GH, Ahn KM. Park HI, et al. J Korean Assoc Oral Maxillofac Surg. 2023 Aug 31;49(4):228-232. doi: 10.5125/jkaoms.2023.49.4.228. J Korean Assoc Oral Maxillofac Surg. 2023. PMID: 37641907 Free PMC article.

2

KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature.

Choi Y, Choi J, Do H, Hwang S, Seo GH, Choi IH, Keum C, Choi JH, Kang M, Kim GH, Yoo HW, Lee BH. Choi Y, et al. Mol Genet Genomic Med. 2023 Apr;11(4):e2127. doi: 10.1002/mgg3.2127. Epub 2022 Dec 23. Mol Genet Genomic Med. 2023. PMID: 36564961 Free PMC article. Review.

3

Clinical and molecular spectra of BRAF-associated RASopathy.

Lee Y, Choi Y, Seo GH, Kim GH, Choi IH, Keum C, Ko JM, Cheon CK, Jeon J, Choi JH, Yoo HW, Lee BH. Lee Y, et al. J Hum Genet. 2021 Apr;66(4):389-399. doi: 10.1038/s10038-020-00852-3. Epub 2020 Oct 10. J Hum Genet. 2021. PMID: 33040082

4

Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents.

Kim JH, Choi Y, Hwang S, Yoon JH, Kim GH, Yoo HW, Choi JH. Kim JH, et al. Exp Clin Endocrinol Diabetes. 2023 Oct;131(10):515-522. doi: 10.1055/a-2127-9292. Epub 2023 Jul 12. Exp Clin Endocrinol Diabetes. 2023. PMID: 37437600

5

Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome.

Kim JH, Kim GH, Yoo HW, Choi JH. Kim JH, et al. Ann Pediatr Endocrinol Metab. 2023 Jun;28(2):77-86. doi: 10.6065/apem.2346108.054. Epub 2023 Jun 30. Ann Pediatr Endocrinol Metab. 2023. PMID: 37401054 Free PMC article.

6

Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Choi JH, Kim GH, Yoo HW. Choi JH, et al. Ann Pediatr Endocrinol Metab. 2016 Mar;21(1):1-6. doi: 10.6065/apem.2016.21.1.1. Epub 2016 Mar 31. Ann Pediatr Endocrinol Metab. 2016. PMID: 27104172 Free PMC article. Review.

7

Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome.

Kim HY, Shin CH, Lee YA, Shin CH, Kim GH, Ko JM. Kim HY, et al. Ann Lab Med. 2022 Nov 1;42(6):668-677. doi: 10.3343/alm.2022.42.6.668. Ann Lab Med. 2022. PMID: 35765875 Free PMC article.

8

A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutation.

Kim YM, Kang M, Choi JH, Lee BH, Kim GH, Ohn JH, Kim SY, Park MS, Yoo HW. Kim YM, et al. Metabolism. 2014 Jan;63(1):42-9. doi: 10.1016/j.metabol.2013.08.015. Epub 2013 Oct 18. Metabolism. 2014. PMID: 24140098 Review.

9

Unfavorable clinical outcomes in patients with carbamoyl phosphate synthetase 1 deficiency.

Choi Y, Oh A, Lee Y, Kim GH, Choi JH, Yoo HW, Lee BH. Choi Y, et al. Clin Chim Acta. 2022 Feb 1;526:55-61. doi: 10.1016/j.cca.2021.11.029. Epub 2021 Dec 29. Clin Chim Acta. 2022. PMID: 34973183

10

Endocrine dysfunctions in children with Williams-Beuren syndrome.

Kim YM, Cho JH, Kang E, Kim GH, Seo EJ, Lee BH, Choi JH, Yoo HW. Kim YM, et al. Ann Pediatr Endocrinol Metab. 2016 Mar;21(1):15-20. doi: 10.6065/apem.2016.21.1.15. Epub 2016 Mar 31. Ann Pediatr Endocrinol Metab. 2016. PMID: 27104174 Free PMC article.

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