Search

  • HOME
  • Search
Original Articles
Molecular Genetic Studies on the Human CYP21A2 Gene (1).
Byung Kiu Park, Hyang Ok Woo, Han Wook Woo
Endocrinol Metab. 1994;9(3):219-227.   Published online November 6, 2019
PDFPDF    
Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Eun Yeong Mo, Ji-young Lee, Su Yeon Kim et al.
Endocrinol Metab. 2018;33(3):413-422.   Published online September 18, 2018
Full textFull text    PubreaderPubReader    CrossRef-TDMCrossref - TDM    PDFPDF    
Case Reports
Untreated Congenital Adrenal Hyperplasia with 17-α Hydroxylase/17,20-Lyase Deficiency Presenting as Massive Adrenocortical Tumor
Su Jin Lee, Je Eun Song, Sena Hwang et al.
Endocrinol Metab. 2015;30(3):408-413.   Published online August 4, 2015
Full textFull text    PubreaderPubReader    CrossRef-TDMCrossref - TDM    PDFPDF    
Review Articles
ACTH-Independent Macronodular Adrenal Hyperplasia.
Livia M Mermejo, Tania L Mazzuco, Solange Grunenwald, Maria Candida B V Fragoso, Isabelle Bourdeau, Andre Lacroix
Endocrinol Metab. 2011;26(1):1-11.   Published online March 1, 2011
PDFPDF    
Original Articles
Six Cases of Congenital Adrenal Hyperplasia That Were Due to 17alpha-hydroxylase/17,20-lyase Deficiency.
Dong Hoon Shin, Sung Hoon Yu, Young Min Choi et al.
Endocrinol Metab. 2009;24(2):109-115.   Published online June 1, 2009
PDFPDF    
Case Reports
A Case of Congenital Adrenal Hyperplasia Combined with a Testicular Adrenal Rest Tumor and Adrenal Incidentaloma.
Gyu Rang Cho, Hee Won Chueh, Jung Pyo Kim et al.
Endocrinol Metab. 2007;22(5):365-370.   Published online October 1, 2007
PDFPDF    
Two Cases of Simple Virilizing Congenital Adrenal Hyperplasia with Compound Heterozygous Mutations of CYP21 Gene.
Koon Soon Kim, Yun Sun Choi, Youn Sun Bai, So Young Rha, Young Suk Jo, Minho Shong
Endocrinol Metab. 2007;22(4):299-304.   Published online August 1, 2007
PDFPDF    
Original Articles
A Clinical Observation on Twelve Cases of Primary Aldosteronism.
Seung Chul Cho, Yong Soo Park, Hwon Gyum Park et al.
Endocrinol Metab. 2004;19(2):194-202.   Published online April 1, 2004
PDFPDF    
Case Reports
A Case of Congenital Adrenal Hyperplasia due to 11beta-Hydroxylase Deficiency.
Ohk Hyun Ryu, Hye Jin Yoo, Soo Yeon Park et al.
Endocrinol Metab. 2004;19(1):58-63.   Published online February 1, 2004
PDFPDF    
A Case of AVP Dependent Bilateral Macronodular Adrenal Hyperplasia.
Hyun Jin Kim, Se Hwa Kim, Yu Mie Rhee et al.
Endocrinol Metab. 2002;17(4):603-609.   Published online August 1, 2002
PDFPDF    
A Case of Bilateral Macronodular Adrenal Hyperplasia with Cushing's Syndrome Treated by Unilateral Adrenalectomy.
Si Hoon Lee, Kwang Eun Lee, Eun Seok Kang et al.
Endocrinol Metab. 2002;17(4):596-602.   Published online August 1, 2002
PDFPDF    
A Case of Primary Amenorrhea due to 17 -Hydroxylase Deficiency.
Hong Seub Rim, Seon Hwa Lee, Jung Min Hong et al.
Endocrinol Metab. 2001;16(1):130-133.   Published online February 1, 2001
PDFPDF    
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
PDFPDF    

Endocrinology
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: journal@endocrinology.or.kr                

Copyright © 2020 by Korean Endocrine Society. All rights reserved.

Developed in M2community

Close layer
prev next