Lim HH - Search Results

1

A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1.

Jwa HJ, Lee KS, Kim GH, Yoo HW, Lim HH. Jwa HJ, et al. Among authors: lim hh. Korean J Pediatr. 2014 Sep;57(9):416-9. doi: 10.3345/kjp.2014.57.9.416. Epub 2014 Sep 30. Korean J Pediatr. 2014. PMID: 25324868 Free PMC article.

2

Risk factor for pituitary dysfunction in children and adolescents with Rathke's cleft cysts.

Lim HH, Yang SW. Lim HH, et al. Korean J Pediatr. 2010 Jul;53(7):759-65. doi: 10.3345/kjp.2010.53.7.759. Epub 2010 Jul 31. Korean J Pediatr. 2010. PMID: 21189952 Free PMC article.

3

Prevalence and risk factors of the metabolic syndrome in young adults with childhood-onset hypopituitary growth hormone deficiency.

Lim HH, Kang MJ, Yun IS, Lee YA, Shin CH, Yang SW. Lim HH, et al. Korean J Pediatr. 2010 Oct;53(10):892-7. doi: 10.3345/kjp.2010.53.10.892. Epub 2010 Oct 31. Korean J Pediatr. 2010. PMID: 21189960 Free PMC article.

4

The difference in serum alkaline phosphatase levels between girls with precocious puberty and those with normal puberty.

Jwa HJ, Yang SI, Lim HH. Jwa HJ, et al. Among authors: lim hh. Ann Pediatr Endocrinol Metab. 2013 Dec;18(4):191-5. doi: 10.6065/apem.2013.18.4.191. Epub 2013 Dec 31. Ann Pediatr Endocrinol Metab. 2013. PMID: 24904876 Free PMC article.

5

Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review.

An SJ, Kim SZ, Kim GH, Yoo HW, Lim HH. An SJ, et al. Among authors: lim hh. Korean J Pediatr. 2016 Nov;59(Suppl 1):S45-S48. doi: 10.3345/kjp.2016.59.11.S45. Epub 2016 Nov 30. Korean J Pediatr. 2016. PMID: 28018444 Free PMC article.

6

First Case of Peroxisomal D-bifunctional Protein Deficiency with Novel HSD17B4 Mutations and Progressive Neuropathy in Korea.

Bae EY, Yi Y, Lim HH, Lee JM, Lee B, Kim SY, Kim YM. Bae EY, et al. Among authors: lim hh. J Korean Med Sci. 2020 Oct 12;35(39):e357. doi: 10.3346/jkms.2020.35.e357. J Korean Med Sci. 2020. PMID: 33045774 Free PMC article.

7

Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype.

Choi JH, Lee BH, Heo SH, Kim GH, Kim YM, Kim DS, Ko JM, Sohn YB, Hong YH, Lee DH, Kook H, Lim HH, Kim KH, Kim WS, Hong GR, Kim SH, Park SH, Kim CD, Kim SM, Seo JS, Yoo HW. Choi JH, et al. Among authors: lim hh. Medicine (Baltimore). 2017 Jul;96(29):e7387. doi: 10.1097/MD.0000000000007387. Medicine (Baltimore). 2017. PMID: 28723748 Free PMC article.

8

Association of Early Pubertal Onset in Female Rats With Inhalation of Lavender Oil.

Kim YM, Lim HH. Kim YM, et al. Among authors: lim hh. J Korean Med Sci. 2022 Jan 10;37(2):e9. doi: 10.3346/jkms.2022.37.e9. J Korean Med Sci. 2022. PMID: 35014224 Free PMC article.

9

Growth Responses During 3 Years of Growth Hormone Treatment in Children and Adolescents With Growth Hormone Deficiency: Comparison Between Idiopathic, Organic and Isolated Growth Hormone Deficiency, and Multiple Pituitary Hormone Deficiency.

Lim HH, Kim YM, Lee GM, Yu J, Han HS, Yu J. Lim HH, et al. J Korean Med Sci. 2022 Mar 21;37(11):e90. doi: 10.3346/jkms.2022.37.e90. J Korean Med Sci. 2022. PMID: 35315601 Free PMC article.

10

The GBA p.G85E mutation in Korean patients with non-neuronopathic Gaucher disease: founder and neuroprotective effects.

Kim YM, Choi JH, Kim GH, Sohn YB, Ko JM, Lee BH, Cheon CK, Lim HH, Heo SH, Yoo HW. Kim YM, et al. Among authors: lim hh. Orphanet J Rare Dis. 2020 Nov 11;15(1):318. doi: 10.1186/s13023-020-01597-0. Orphanet J Rare Dis. 2020. PMID: 33176831 Free PMC article.

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