Lee YM - Search Results

1

Nusinersen for spinal muscular atrophy types II and III: a retrospective single-center study in South Korea.

Shin HJ, Na JH, Lee H, Lee YM. Shin HJ, et al. Among authors: lee ym, lee h. World J Pediatr. 2023 May;19(5):450-459. doi: 10.1007/s12519-022-00638-x. Epub 2022 Nov 28. World J Pediatr. 2023. PMID: 36441395

2

Genotype-phenotype correlations in pediatric patients with myotonic dystrophy type 1.

Kim HJ, Na JH, Lee YM. Kim HJ, et al. Among authors: lee ym. Korean J Pediatr. 2019 Feb;62(2):55-61. doi: 10.3345/kjp.2018.06919. Epub 2018 Sep 23. Korean J Pediatr. 2019. PMID: 30304901 Free PMC article.

3

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.

4

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.

5

Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction.

Na JH, Kim HD, Lee YM. Na JH, et al. Among authors: lee ym. Ther Adv Neurol Disord. 2020 Feb 6;13:1756286419897813. doi: 10.1177/1756286419897813. eCollection 2020. Ther Adv Neurol Disord. 2020. PMID: 32082420 Free PMC article.

6

Clinical Characteristics of Early-Onset and Late-Onset Leigh Syndrome.

Hong CM, Na JH, Park S, Lee YM. Hong CM, et al. Among authors: lee ym. Front Neurol. 2020 Apr 15;11:267. doi: 10.3389/fneur.2020.00267. eCollection 2020. Front Neurol. 2020. PMID: 32351444 Free PMC article.

7

Central precocious puberty may be a manifestation of endocrine dysfunction in pediatric patients with mitochondrial disease.

Chae HW, Na JH, Kwon A, Kim HS, Lee YM. Chae HW, et al. Among authors: lee ym. Eur J Pediatr. 2021 Feb;180(2):425-432. doi: 10.1007/s00431-020-03804-3. Epub 2020 Sep 10. Eur J Pediatr. 2021. PMID: 32914201

8

Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndrome.

Chae HW, Na JH, Kim HS, Lee YM. Chae HW, et al. Among authors: lee ym. Eur J Endocrinol. 2020 Nov;183(5):505-512. doi: 10.1530/EJE-20-0189. Eur J Endocrinol. 2020. PMID: 33107434

9

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.

10

Jacobsen syndrome with bilateral periventricular white matter lesions.

Lee HJ, Lee HI, Na JH, Lee YM. Lee HJ, et al. Among authors: lee ym, lee hi. World J Pediatr. 2022 Feb;18(2):142-143. doi: 10.1007/s12519-021-00467-4. Epub 2021 Dec 3. World J Pediatr. 2022. PMID: 34860330 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,214 results

Search Page

Filters