• HOME
  • Search
Case Reports
A Case of Familial Multiple Endocrine Neoplasia Type 1 with a Novel Mutation in the MEN1 Gene.
Min Jung Kim, Eun Hee Kim, Mi Seon Shin et al.
Endocrinol Metab. 2011;26(2):171-176.   Published online June 1, 2011
A Case of Type Ia Glycogen Storage Disease Diagnosed in the Military Hospital.
Tae Woong Lee, Sang Youl Rhee, Joo Young Kim et al.
Endocrinol Metab. 2011;26(1):84-88.   Published online March 1, 2011
The Case of Accelerated Linear Growth Despite Growth Hormone and Insulin-like Growth Factor-I Deficiency.
Kyeong Ju Lee, Jong Ryeal Hahm, Tae Sik Jung et al.
Endocrinol Metab. 2009;24(3):206-211.   Published online September 1, 2009
Review Articles
Molecular Genetic Defects of Pituitary Transcription Factor Genes in Combined Pituitary Hormone Deficiency.
Han Wook Yoo
Endocrinol Metab. 2003;18(6):532-542.   Published online December 1, 2003
Original Articles
A Study on the Relationship Between Genotype and Phenotype in Korean Patients with Congenital Adrenogenital Syndrome Caused by 21-hydroxylase Deficiency.
Dong Kyu Jin, Jung Sim Kim, Seung Mi Song et al.
Endocrinol Metab. 2000;15(2):237-247.   Published online January 1, 2001
Clinical Effects of E. cole Derived Authentic REcombinant Human Growth Hormone(DA-3002) in Children with Growth Hormone Deficiency.
Se Won Yang, Byung Chul Lee, Chul Woo Ko, Duk Hee Kim, Han Wook Yoo, Woo Young Chung
Endocrinol Metab. 1998;13(4):526-535.   Published online January 1, 2001

and Metabolism

Print ISSN: 2093-596X
Online ISSN: 2093-5978

Editorial Office
101-2503, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea​
Tel: +82-2-716-2428    Fax: +82-2-714-5103    E-mail:                

Copyright © 2022 by Korean Endocrine Society.

Developed in M2PI