Kim J - Search Results

1

Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.

Kim SJ, Kwak HH, Cho SY, Sohn YB, Park SW, Huh R, Kim J, Ko AR, Jin DK. Kim SJ, et al. Among authors: kim j. Mol Pharm. 2015 Oct 5;12(10):3759-65. doi: 10.1021/acs.molpharmaceut.5b00550. Epub 2015 Sep 21. Mol Pharm. 2015. PMID: 26370910

2

Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases.

Kim H, Kim J, Huh R, Cho SY, Jin DK. Kim H, et al. Among authors: kim j. Ann Pediatr Endocrinol Metab. 2015 Jun;20(2):106-9. doi: 10.6065/apem.2015.20.2.106. Epub 2015 Jun 30. Ann Pediatr Endocrinol Metab. 2015. PMID: 26191516 Free PMC article.

3

Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome.

Huh R, Cho SY, Kim J, Ki CS, Jin DK. Huh R, et al. Among authors: kim j. Ann Clin Lab Sci. 2015 Summer;45(4):458-61. Ann Clin Lab Sci. 2015. PMID: 26275701

4

First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review.

Park EG, Cho SY, Lee J, Kim J, Cho H, Kim J, Huh R, Ki CS, Kim OH, Jin DK. Park EG, et al. Among authors: kim oh, kim j. Ann Clin Lab Sci. 2016 May;46(3):302-7. Ann Clin Lab Sci. 2016. PMID: 27312557 Review.

5

Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.

Cho EK, Kim J, Yang A, Ki CS, Lee JE, Cho SY, Jin DK. Cho EK, et al. Among authors: kim j. Orphanet J Rare Dis. 2016 Aug 9;11(1):113. doi: 10.1186/s13023-016-0496-x. Orphanet J Rare Dis. 2016. PMID: 27506760 Free PMC article.

6

Report of 5 novel mutations of the α-L-iduronidase gene and comparison of Korean mutations in relation with those of Japan or China in patients with mucopolysaccharidosis I.

Kwak MJ, Huh R, Kim J, Park HD, Cho SY, Jin DK. Kwak MJ, et al. Among authors: kim j. BMC Med Genet. 2016 Aug 12;17(1):58. doi: 10.1186/s12881-016-0319-x. BMC Med Genet. 2016. PMID: 27520059 Free PMC article.

7

Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis.

Yang M, Cho SY, Park HD, Choi R, Kim YE, Kim J, Lee SY, Ki CS, Kim JW, Sohn YB, Song J, Jin DK. Yang M, et al. Among authors: kim j, kim ye, kim jw. Orphanet J Rare Dis. 2017 Jan 17;12(1):11. doi: 10.1186/s13023-016-0556-2. Orphanet J Rare Dis. 2017. PMID: 28095893 Free PMC article.

8

Further delineation of COG8-CDG: A case with novel compound heterozygous mutations diagnosed by targeted exome sequencing.

Yang A, Cho SY, Jang JH, Kim J, Kim SZ, Lee BH, Yoo HW, Jin DK. Yang A, et al. Among authors: kim sz, kim j. Clin Chim Acta. 2017 Aug;471:191-195. doi: 10.1016/j.cca.2017.06.010. Epub 2017 Jun 13. Clin Chim Acta. 2017. PMID: 28619360

9

2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis.

Cho EK, Kim J, Yang A, Cho SY, Jin DK. Cho EK, et al. Among authors: kim j. Ann Pediatr Endocrinol Metab. 2017 Jun;22(2):129-132. doi: 10.6065/apem.2017.22.2.129. Epub 2017 Jun 28. Ann Pediatr Endocrinol Metab. 2017. PMID: 28690993 Free PMC article.

10

Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience.

Yang A, Kim J, Cho SY, Jin DK. Yang A, et al. Among authors: kim j. Orphanet J Rare Dis. 2017 Aug 30;12(1):146. doi: 10.1186/s13023-017-0702-5. Orphanet J Rare Dis. 2017. PMID: 28854950 Free PMC article.

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