Kim YM - Search Results

1

Phenotype categorization of neurofibromatosis type I and correlation to NF1 mutation types.

Kang E, Kim YM, Seo GH, Oh A, Yoon HM, Ra YS, Kim EK, Kim H, Heo SH, Kim GH, Osborn MJ, Tolar J, Yoo HW, Lee BH. Kang E, et al. Among authors: kim h, kim gh, kim ym, kim ek. J Hum Genet. 2020 Jan;65(2):79-89. doi: 10.1038/s10038-019-0695-0. Epub 2019 Nov 28. J Hum Genet. 2020. PMID: 31776437

2

Characteristic dysmorphic features in congenital disorders of glycosylation type IIb.

Kim YM, Seo GH, Jung E, Jang JH, Kim SZ, Lee BH. Kim YM, et al. Among authors: kim sz. J Hum Genet. 2018 Mar;63(3):383-386. doi: 10.1038/s10038-017-0386-7. Epub 2017 Dec 13. J Hum Genet. 2018. PMID: 29235540 Review.

3

Biochemical and molecular characterisation of neurological Wilson disease.

Seo GH, Kim YM, Oh SH, Chung SJ, Choi IH, Kim GH, Yum MS, Choi JH, Kim KM, Ko TS, Lee BH, Yoo HW. Seo GH, et al. Among authors: kim gh, kim km, kim ym. J Med Genet. 2018 Sep;55(9):587-593. doi: 10.1136/jmedgenet-2017-105214. Epub 2018 Apr 4. J Med Genet. 2018. PMID: 29618506

4

The phenotypic heterogeneity of patients with Marfan-related disorders and their variant spectrums.

Seo GH, Kim YM, Kang E, Kim GH, Seo EJ, Lee BH, Choi JH, Yoo HW. Seo GH, et al. Among authors: kim gh, kim ym. Medicine (Baltimore). 2018 May;97(20):e10767. doi: 10.1097/MD.0000000000010767. Medicine (Baltimore). 2018. PMID: 29768367 Free PMC article.

5

Low prevalence of argininosuccinate lyase deficiency among inherited urea cycle disorders in Korea.

Kim D, Ko JM, Kim YM, Seo GH, Kim GH, Lee BH, Yoo HW. Kim D, et al. Among authors: kim gh, kim ym. J Hum Genet. 2018 Jul;63(8):911-917. doi: 10.1038/s10038-018-0467-2. Epub 2018 May 17. J Hum Genet. 2018. PMID: 29773863

6

Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.

Kang E, Kim YM, Choi Y, Lee Y, Kim J, Choi IH, Yoo HW, Yoon HM, Lee BH. Kang E, et al. Among authors: kim ym, kim j. Orphanet J Rare Dis. 2022 Jan 29;17(1):24. doi: 10.1186/s13023-022-02174-3. Orphanet J Rare Dis. 2022. PMID: 35093157 Free PMC article.

7

Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.

Choi JH, Jung CW, Kang E, Kim YM, Heo SH, Lee BH, Kim GH, Yoo HW. Choi JH, et al. Among authors: kim gh, kim ym. Yonsei Med J. 2017 May;58(3):527-532. doi: 10.3349/ymj.2017.58.3.527. Yonsei Med J. 2017. PMID: 28332357 Free PMC article.

8

Long-term Consequences of Congenital Adrenal Hyperplasia due to Classic 21-hydroxylase Deficiency in Adolescents and Adults.

Kim JH, Choi JH, Kang E, Kim YM, Lee BH, Yoo HW. Kim JH, et al. Among authors: kim ym. Exp Clin Endocrinol Diabetes. 2017 Mar;125(3):196-201. doi: 10.1055/s-0042-123037. Epub 2017 Jan 10. Exp Clin Endocrinol Diabetes. 2017. PMID: 28073127

9

Mutation Spectrum of STAR and a Founder Effect of the p.Q258* in Korean Patients with Congenital Lipoid Adrenal Hyperplasia.

Kang E, Kim YM, Kim GH, Lee BH, Yoo HW, Choi JH. Kang E, et al. Among authors: kim gh, kim ym. Mol Med. 2017 Jul;23:149-154. doi: 10.2119/molmed.2017.00023. Epub 2017 May 2. Mol Med. 2017. PMID: 28467518 Free PMC article.

10

Broad clinical spectrum and diverse outcomes of prolactinoma with pediatric onset: medication-resistant and recurrent cases.

Kim YM, Seo GH, Kim YM, Choi JH, Yoo HW. Kim YM, et al. Endocr J. 2018 Mar 28;65(3):307-315. doi: 10.1507/endocrj.EJ17-0268. Epub 2017 Dec 27. Endocr J. 2018. PMID: 29279457 Free article.

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

4,095 results

Search Page

Filters