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Original Articles
Adrenal Gland
2271
Epidemiology and Long-Term Adverse Outcomes in Korean Patients with Congenital Adrenal Hyperplasia: A Nationwide Study
Jung Hee Kim, Sunkyu Choi, Young Ah Lee, Juneyoung Lee, Sin Gon Kim
Endocrinol Metab. 2022;37(1):138-147.   Published online February 28, 2022
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Adrenal Gland
2257
Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency
Taek Min Kim, Jung Hee Kim, Han Na Jang, Man Ho Choi, Jeong Yeon Cho, Sang Youn Kim
Endocrinol Metab. 2022;37(1):124-137.   Published online February 8, 2022
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Review Articles
Thyroid
2177
Antithyroid Drug Treatment in Graves’ Disease
Jae Hoon Chung
Endocrinol Metab. 2021;36(3):491-499.   Published online June 16, 2021
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2068
WD40-Repeat Proteins in Ciliopathies and Congenital Disorders of Endocrine System
Yeonjoo Kim, Soo-Hyun Kim
Endocrinol Metab. 2020;35(3):494-506.   Published online September 8, 2020
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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
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Endocrine Research
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
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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
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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
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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
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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
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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
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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
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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
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New Mutation Site in Vasopressin V2 Receptor Gene in a Family with Congenital Nephrogenic Diabetes Incipidus.
Soon Hee Lee, Chang Hoon Choi, See Hyung Park et al.
Endocrinol Metab. 2000;15(1):97-106.   Published online January 1, 2001
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Endocrinology
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