Annals of Pediatric Endocrinology & Metabolism


Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam: Khanh Ngoc Nguyen, Giang Thi Kim Dang, Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Mai Nguyen Thi Phuong, Huong Thu Pham, Ngoc Diem Ngo, Dung Chi Vu; Ann Pediatr Endocrinol Metab. 2025;30(6):330-339. Published online May 7, 2025; DOI: https://doi.org/10.6065/apem.2448292.146; Full text PubReader ePub PDF Supplementary Material


Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene: Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2024;29(1):54-59. Published online February 29, 2024; DOI: https://doi.org/10.6065/apem.2346014.007
Web of Science 3 Crossref 4; Full text PubReader ePub PDF


Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome: Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2023;28(2):77-86. Published online June 30, 2023; DOI: https://doi.org/10.6065/apem.2346108.054
Web of Science 7 Crossref 8; Full text PubReader ePub PDF


Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2016;21(1):1-6. Published online March 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.1.1
Crossref 22; Full text PubReader ePub PDF


The Behavioral and Psychic Masculinizing Scores and Its Related Factors in Female Patients with Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency.: Il Tae Hwang, Seong Gon Ryu, Kyung Hee Yi; Ann Pediatr Endocrinol Metab. 2005;10(1):64-70.; PDF


Genotype of Steroid 21-Hydroxylase Gene and Clinical Characteristics in Patients with Congenital Adrenal Hyperplasia 21-Hydroxylase Deficiency.: Jung Min Ko, Jin Ho Choi, Gu Hwan Kim, Han Wook Yoo; Ann Pediatr Endocrinol Metab. 2005;10(1):57-63.; PDF

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