Lee JE - Search Results

1

Successful dialysis in a boy with methylmalonic acidemia.

Paik KH, Lee JE, Jin DK. Paik KH, et al. Among authors: lee je. Pediatr Nephrol. 2004 Oct;19(10):1180-1. doi: 10.1007/s00467-003-1409-5. Epub 2004 Feb 21. Pediatr Nephrol. 2004. PMID: 14986089 No abstract available.

2

Correlation between fasting plasma ghrelin levels and age, body mass index (BMI), BMI percentiles, and 24-hour plasma ghrelin profiles in Prader-Willi syndrome.

Paik KH, Jin DK, Song SY, Lee JE, Ko SH, Song SM, Kim JS, Oh YJ, Kim SW, Lee SH, Kim SH, Kwon EK, Choe YH. Paik KH, et al. Among authors: lee sh, lee je. J Clin Endocrinol Metab. 2004 Aug;89(8):3885-9. doi: 10.1210/jc.2003-032137. J Clin Endocrinol Metab. 2004. PMID: 15292322

3

Peptide YY, cholecystokinin, insulin and ghrelin response to meal did not change, but mean serum levels of insulin is reduced in children with Prader-Willi syndrome.

Paik KH, Jin DK, Lee KH, Armstrong L, Lee JE, Oh YJ, Kim S, Kwon EK, Choe YH. Paik KH, et al. Among authors: lee je, lee kh. J Korean Med Sci. 2007 Jun;22(3):436-41. doi: 10.3346/jkms.2007.22.3.436. J Korean Med Sci. 2007. PMID: 17596650 Free PMC article.

4

Improvement of cardiac function by short-term enzyme replacement therapy in a murine model of cardiomyopathy associated with Hunter syndrome evaluated by serial echocardiography with speckle tracking 2-D strain analysis.

Lee SC, Lee J, Jin DK, Kim JS, Jeon ES, Kwun YH, Chang MS, Ko AR, Yook YJ, Sohn YB. Lee SC, et al. Mol Genet Metab. 2014 Jul;112(3):218-23. doi: 10.1016/j.ymgme.2014.04.005. Epub 2014 Apr 30. Mol Genet Metab. 2014. PMID: 24836711

5

Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1.

Wejaphikul K, Cho SY, Huh R, Kwun Y, Lee J, Ki CS, Jin DK. Wejaphikul K, et al. Ann Clin Lab Sci. 2015 Spring;45(2):215-8. Ann Clin Lab Sci. 2015. PMID: 25887879

6

Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNAS.

Lee SH, Mun SH, Cho SY, Kim YJ, Jin DK, Ki CS, Lee JE. Lee SH, et al. Among authors: lee je. Ann Clin Lab Sci. 2015 Spring;45(3):344-7. Ann Clin Lab Sci. 2015. PMID: 26116601

7

Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center.

Yoo Y, Chang MS, Lee J, Cho SY, Park SW, Jin DK, Park HD. Yoo Y, et al. Ann Pediatr Endocrinol Metab. 2013 Sep;18(3):128-34. doi: 10.6065/apem.2013.18.3.128. Epub 2013 Sep 30. Ann Pediatr Endocrinol Metab. 2013. PMID: 24904866 Free PMC article.

8

Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome.

Sohn YB, Cho SY, Lee J, Kwun Y, Huh R, Jin DK. Sohn YB, et al. Mol Genet Metab. 2015 Feb;114(2):156-60. doi: 10.1016/j.ymgme.2014.08.009. Epub 2014 Aug 30. Mol Genet Metab. 2015. PMID: 25219292 Clinical Trial.

9

An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing.

Kim J, Cho SY, Yang A, Jang JH, Choi Y, Lee JE, Jin DK. Kim J, et al. Among authors: lee je. Ann Pediatr Endocrinol Metab. 2017 Sep;22(3):203-207. doi: 10.6065/apem.2017.22.3.203. Epub 2017 Sep 28. Ann Pediatr Endocrinol Metab. 2017. PMID: 29025208 Free PMC article.

10

A case of de novo 18p deletion syndrome with panhypopituitarism.

Yang A, Kim J, Cho SY, Lee JE, Kim HJ, Jin DK. Yang A, et al. Among authors: lee je. Ann Pediatr Endocrinol Metab. 2019 Mar;24(1):60-63. doi: 10.6065/apem.2019.24.1.60. Epub 2019 Mar 31. Ann Pediatr Endocrinol Metab. 2019. PMID: 30943682 Free PMC article.

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