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Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review
Jihyun Ha, Yunha Choi,, Mo Kyung Jung, Eun-Gyong Yoo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2024;29(1):60-66.   Published online February 29, 2024
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A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets
In Hwa Jeong, Jae-Ho Yoo, Namhee Kim
Ann Pediatr Endocrinol Metab. 2021;26(2):130-133.   Published online June 30, 2021
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Limitations of current screening methods for lipid disorders in Korean adolescents and a proposal for an effective detection method: a nationwide, cross-sectional study
Jung Hyun Shin, Ji In Cheong, Hee Won Cheuh, Jae-Ho Yoo
Ann Pediatr Endocrinol Metab. 2020;25(4):265-271.   Published online December 31, 2020
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Primary hyperparathyroidism versus familial hypocalciuric hypercalcemia: a challenging diagnostic evaluation in an adolescent female
Mustafa Tosur, Monica E. Lopez, David L. Paul
Ann Pediatr Endocrinol Metab. 2019;24(3):195-198.   Published online September 30, 2019
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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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Response of Growth Hormone Treatment to Final Height in Children with Growth Hormone Deficiency and Familial Short Stature.
Duk Hee Kim, Hae Jung Shin, So Chung Chung, Mee Jung Park
Ann Pediatr Endocrinol Metab. 1999;4(2):159-169.
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