Lee YM - Search Results

1

Ophthalmological manifestations in patients with Leigh syndrome.

Han J, Lee YM, Kim SM, Han SY, Lee JB, Han SH. Han J, et al. Among authors: lee ym, lee jb. Br J Ophthalmol. 2015 Apr;99(4):528-35. doi: 10.1136/bjophthalmol-2014-305704. Epub 2014 Oct 28. Br J Ophthalmol. 2015. PMID: 25351680

2

Ophthalmoplegia in Mitochondrial Disease.

Lee SJ, Na JH, Han J, Lee YM. Lee SJ, et al. Among authors: lee ym. Yonsei Med J. 2018 Dec;59(10):1190-1196. doi: 10.3349/ymj.2018.59.10.1190. Yonsei Med J. 2018. PMID: 30450853 Free PMC article.

3

Lennox-Gastaut Syndrome in Mitochondrial Disease.

Lee S, Baek MS, Lee YM. Lee S, et al. Among authors: lee ym. Yonsei Med J. 2019 Jan;60(1):106-114. doi: 10.3349/ymj.2019.60.1.106. Yonsei Med J. 2019. PMID: 30554497 Free PMC article.

4

Magnetic resonance spectroscopy in Leigh-MELAS overlap syndrome.

Ko A, Lee YM. Ko A, et al. Among authors: lee ym. World J Pediatr. 2019 Jun;15(3):306-308. doi: 10.1007/s12519-019-00250-6. Epub 2019 Apr 9. World J Pediatr. 2019. PMID: 30968306 No abstract available.

5

Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations.

Lee S, Na JH, Lee YM. Lee S, et al. Among authors: lee ym. Front Neurol. 2019 May 8;10:496. doi: 10.3389/fneur.2019.00496. eCollection 2019. Front Neurol. 2019. PMID: 31139141 Free PMC article.

6

DYNC2H1 variants cause Leber congenital amaurosis without syndromic features.

Lee J, Lee H, Lee YM, Kuht HJ, Thomas MG, Kim SJ, Lee ST, Han J. Lee J, et al. Among authors: lee ym, lee h, lee st. Clin Genet. 2021 Jul;100(1):111-113. doi: 10.1111/cge.13958. Epub 2021 Mar 23. Clin Genet. 2021. PMID: 33755199 No abstract available.

7

Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome.

Na JH, Lee YM. Na JH, et al. Among authors: lee ym. Acta Neurol Scand. 2022 Apr;145(4):414-422. doi: 10.1111/ane.13566. Epub 2021 Dec 7. Acta Neurol Scand. 2022. PMID: 34877647

8

Mitochondrial respiratory chain defects: underlying etiology in various epileptic conditions.

Lee YM, Kang HC, Lee JS, Kim SH, Kim EY, Lee SK, Slama A, Kim HD. Lee YM, et al. Among authors: lee js, lee sk. Epilepsia. 2008 Apr;49(4):685-90. doi: 10.1111/j.1528-1167.2007.01522.x. Epub 2008 Feb 5. Epilepsia. 2008. PMID: 18266755 Free article.

9

Neuroradiologic findings in children with mitochondrial disorder: correlation with mitochondrial respiratory chain defects.

Kim J, Lee SK, Kim EY, Kim DI, Lee YM, Lee JS, Kim HD. Kim J, et al. Among authors: lee ym, lee js, lee sk. Eur Radiol. 2008 Aug;18(8):1741-8. doi: 10.1007/s00330-008-0921-1. Epub 2008 Apr 4. Eur Radiol. 2008. PMID: 18389251

10

A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency.

Seo JH, Lee YM, Lee JS, Kim SH, Kim HD. Seo JH, et al. Among authors: lee ym, lee js. Brain Dev. 2010 Mar;32(3):253-7. doi: 10.1016/j.braindev.2008.12.020. Epub 2009 Feb 23. Brain Dev. 2010. PMID: 19233577

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