Annals of Pediatric Endocrinology & Metabolism


The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea: Sukdong Yoo, Ju Young Yoon, Changwon Keum, Chong Kun Cheon; Ann Pediatr Endocrinol Metab. 2023;28(1):54-60. Published online January 18, 2022; DOI: https://doi.org/10.6065/apem.2142116.058; Full text PubReader ePub PDF Supplementary Material


Treatment of congenital hypogonadotropic hypogonadism in male patients: Hae Sang Lee, Young Suk Shim, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2022;27(3):176-182. Published online September 30, 2022; DOI: https://doi.org/10.6065/apem.2244208.104
Web of Science 3 Crossref 3; Full text PubReader ePub PDF


Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita: Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Kyung Chul Song, Jin-Sung Lee, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2021;26(2):126-129. Published online June 30, 2021; DOI: https://doi.org/10.6065/apem.2040088.044
Web of Science 2 Crossref 2; Full text PubReader ePub PDF


Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an FGFR1 gene variant: Jaewon Choe, Jae Hyun Kim, Young Ah Kim, Jieun Lee; Ann Pediatr Endocrinol Metab. 2020;25(3):192-197. Published online July 29, 2020; DOI: https://doi.org/10.6065/apem.1938148.074
Web of Science 2 Crossref 2; Full text PubReader ePub PDF


Delayed puberty versus hypogonadism: a challenge for the pediatrician: Mauro Bozzola, Elena Bozzola, Chiara Montalbano, Filomena Andreina Stamati, Pietro Ferrara, Alberto Villani; Ann Pediatr Endocrinol Metab. 2018;23(2):57-61. Published online June 20, 2018; DOI: https://doi.org/10.6065/apem.2018.23.2.57
Web of Science 22 Crossref 24; Full text PubReader ePub PDF


Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience: Sun-Jeong Shin, Yeonah Sul, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Jae Hyun Kim, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2015;20(1):27-33. Published online March 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.1.27
Crossref 24; Full text PubReader ePub PDF


A Case of Extreme Uterine Hypotrophy in Hypogonadotropic Hypogonadism with Partial GH Deficiency.: Se Ra Min, Young Kwang Choo, Hyun Seok Cho, Hyeon Soo Lee, Ja Kyoung Kim, Hyang Ah Lee, Sung Yeon Ahn; Ann Pediatr Endocrinol Metab. 2012;17(2):113-116.; DOI: https://doi.org/10.6065/apem.2012.17.2.113; PDF


Genetic Aspects of Idiopathic Hypogonadotropic Hypogonadism.: Young Lim Shin; Ann Pediatr Endocrinol Metab. 2010;15(3):157-163.; PDF


Hypogonadotropic Hypogonadism and Abnormal Olfactory Bulb Development in CHARGE Syndrome with CHD7 Mutation.: Sun Hyang Lee, Yong Wha Lee, Young Lim Shin; Ann Pediatr Endocrinol Metab. 2009;14(1):68-72.; PDF


Molecular Genetic Analysis and Endocriological Evaluation of Isolated Hypogonadotropic Hypogonadism Presented with Delayed Puberty.: Jung Min Ko, Gu Hwan Kim, Han Wook Yoo; Ann Pediatr Endocrinol Metab. 2007;12(1):41-48.; PDF


A Familial Case of Idiopathic Hypogonadotropic Hypogonadism Occurred in a Boy and His Sister.: Eun Jung Yoo, Kyoung Sim Kim, Yong Wook Kim, Han Wook Yoo, Eun Young Kim; Ann Pediatr Endocrinol Metab. 2006;11(2):199-204.; PDF


Two Cases of Kallmann Syndrome Presented with Delayed Puberty.: Hee Kyoung Choi, Jin Ho Choi, Han Wook Yoo; Ann Pediatr Endocrinol Metab. 2005;10(1):105-109.; PDF


A Case of SRY Positive 46,XX Male.: Na Young Chung, Yeong Heum Yeon, Min Ho Jung, Byung Kyu Suh, Byung Churl Lee; Ann Pediatr Endocrinol Metab. 2003;8(2):184-188.; PDF


Two Cases of Kallmann Syndrome.: Hye Jung Han, Hee Jin Cho, Hye Sun Lee, In Sil Lee, Il Tae Hwang; Ann Pediatr Endocrinol Metab. 2003;8(2):179-183.; PDF

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