Seo GH - 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: seo gh. 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

Turner syndrome presented with tall stature due to overdosage of the SHOX gene.

Seo GH, Kang E, Cho JH, Lee BH, Choi JH, Kim GH, Seo EJ, Yoo HW. Seo GH, et al. Among authors: seo ej. Ann Pediatr Endocrinol Metab. 2015 Jun;20(2):110-3. doi: 10.6065/apem.2015.20.2.110. Epub 2015 Jun 30. Ann Pediatr Endocrinol Metab. 2015. PMID: 26191517 Free PMC article.

3

Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.

Seo GH, Kim JH, Cho JH, Kim GH, Seo EJ, Lee BH, Choi JH, Yoo HW. Seo GH, et al. Among authors: seo ej. Korean J Pediatr. 2016 Jan;59(1):16-23. doi: 10.3345/kjp.2016.59.1.16. Epub 2016 Jan 22. Korean J Pediatr. 2016. PMID: 26893599 Free PMC article.

4

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: seo gh. 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.

5

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. Among authors: seo gh. 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.

6

Long-term endocrine effects and trends in body mass index changes in patients with childhood-onset brain tumors.

Seo GH, Choi JH, Kim YM, Koh KN, Im HJ, Ra YS, Yoo HW. Seo GH, et al. J Neurooncol. 2018 May;138(1):55-62. doi: 10.1007/s11060-018-2765-0. Epub 2018 Jan 19. J Neurooncol. 2018. PMID: 29352447

7

A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing.

Kim YM, Seo GH, Kim GH, Ko JM, Choi JH, Yoo HW. Kim YM, et al. Among authors: seo gh. BMC Med Genet. 2018 Mar 5;19(1):35. doi: 10.1186/s12881-018-0546-4. BMC Med Genet. 2018. PMID: 29506479 Free PMC article.

8

Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report.

Jung D, Seo GH, Kim YM, Choi JH, Yoo HW. Jung D, et al. Among authors: seo gh. Ann Pediatr Endocrinol Metab. 2018 Mar;23(1):51-55. doi: 10.6065/apem.2018.23.1.51. Epub 2018 Mar 22. Ann Pediatr Endocrinol Metab. 2018. PMID: 29609450 Free PMC article.

9

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. 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

10

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: seo ej. Medicine (Baltimore). 2018 May;97(20):e10767. doi: 10.1097/MD.0000000000010767. Medicine (Baltimore). 2018. PMID: 29768367 Free PMC article.

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