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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
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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
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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
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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
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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
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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.
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Genetic Aspects of Idiopathic Hypogonadotropic Hypogonadism.
Young Lim Shin
Ann Pediatr Endocrinol Metab. 2010;15(3):157-163.
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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.
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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.
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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.
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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.
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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.
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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.
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The first case of novel variants of FSHR mutation causing primary amenorrhea in two siblings in Korea
Sukdong Yoo, Ju Young Yoon, Changwon Keum, Chong Kun Cheon
Received May 22, 2021  Accepted August 30, 2021  
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A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patient.
Gimin Lee, Mi Seon Lee, Rosie Lee, Jung Eun Moon
Received February 25, 2022  Accepted May 11, 2022  
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