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Follow-up Study of Hyperthyrotropinemia Detected by Neonatal Screening Test.
Kyung Hoon Paik, Sung Hye Kim, Dong Kyu Jin
Ann Pediatr Endocrinol Metab. 2002;7(2):215-220.
Genetic Analysis in a Case of Transient Neonatal Diabetes Mellitus with Congenital Adrenal Hyperplasia.
Hye Jin Kwon, Jin A Park, Sang Lack Lee, Heung Sik Kim, Dong Seok Jeon, Dong Kyu Jin, Pyoung Han Hwang
Ann Pediatr Endocrinol Metab. 2002;7(1):116-121.
A Case of Follicular Adenoma Occurring in Congenital Goiter due to Dyshormogensis.
Jung Chul Kim, Hyun Seup Sim, Myoung Jea Kang, Dae Yeol Lee
Ann Pediatr Endocrinol Metab. 2002;7(1):112-115.
A Case of Congenital Adrenal Hyperlasia Misdiagnosed as Leydig Cell Tumor.
Marie Kim, Heon Seok Han
Ann Pediatr Endocrinol Metab. 2001;6(2):182-186.
Three Cases of Congenital Adrenal Hyperplasia Owing to Multiple Mutations of CYP21 Gene.
Jun Heo, Jae Hong Yu, Dong Ki Jeong
Ann Pediatr Endocrinol Metab. 2001;6(2):176-181.
Factors Affecting Final Adult Height in Patients with Congenital Hypothyroidism.
Kyoung Lee, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab. 2001;6(1):52-59.
A Molecular Genetic Study with EcoRII Restriction Enzyme on the Steroidogenic Acute Regulatory Protein (StAR) Gene.
Phil Soo Oh, Hye Zin Hwang, Dong Kyu Jin, Jeh Hoon Shin, Hahng Lee
Ann Pediatr Endocrinol Metab. 2000;5(1):115-120.
Two Cases with Prolonged TSH Elevation in Congenital Hypothyroidism.
Jung Ho Seo, Ho Young Yoon, So Mi Park, Hae Jung Shin, Duk Hee Kim
Ann Pediatr Endocrinol Metab. 1999;4(1):109-114.
Children with Congenital Hypothyroidism, Diagnosed After 1 Month of Life.
Jin Soon Hwang, Se Young Kim, Kye Shik Shim, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab. 1998;3(1):73-78.
The Molecular Genetic Study Using Automatic Sequence Analyzer on the Steroidogenic Acute Relulatory Protein(StAR) Gene.
Phil Soo Oh, Hye Zin Hwang, Myung Ryrl Oh, Kye Won Jeon, Jong Sang Ryu, Jeh Hoon Shin, Dong Kyu Jin
Ann Pediatr Endocrinol Metab. 1997;2(1):109-115.
A Study on Subtypes of Thyroid Disorders Detected by Neonatal Screening Test.
Han Jin Kim, Dong Hwan Lee
Ann Pediatr Endocrinol Metab. 1997;2(1):81-100.
Case report describing a patient with diazoxide resistant congenital hyperinsulinism resulting from compound heterozygous mutations in the ABCC8 gene
Kyujung Park, Kyung In Lim, Young Bae Sohn, Hae Sang Lee, Jin Soon Hwang
Received February 25, 2022  Accepted May 11, 2022  
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