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A Leri-Weill dyschondrosteosis patient confirmed by mutation analysis of SHOX gene
Won Bok Choi, Seung Hyeon Seo, Woo Hyun Yoo, Su Young Kim, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2015;20(3):162-165.   Published online September 30, 2015
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Turner syndrome presented with tall stature due to overdosage of the SHOX gene
Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2015;20(2):110-113.   Published online June 30, 2015
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Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases
Hyeseon Kim, Jinsup Kim, Rimm Huh, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2015;20(2):106-109.   Published online June 30, 2015
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Formula fed twin infants with recurrent hypocalcemic seizures with vitamin D deficient rickets and hyperphosphatemia
Byung Wook Jo, Ye Jee Shim, Jin Hyeok Choi, Jun Sik Kim, Hee Joung Lee, Heung Sik Kim
Ann Pediatr Endocrinol Metab. 2015;20(2):102-105.   Published online June 30, 2015
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Massive pericardial effusion and short stature caused by autoimmune hypothyroidism in a 9-year-old girl
Yun Hee Gyon, Heon-Seok Han
Ann Pediatr Endocrinol Metab. 2015;20(2):98-101.   Published online June 30, 2015
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Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a GATA3 mutation
Yong Suk Shim, Woohyeok Choi, Il Tae Hwang, Seung Yang
Ann Pediatr Endocrinol Metab. 2015;20(1):59-63.   Published online March 31, 2015
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Resistance to thyroid hormone due to a novel mutation of thyroid hormone receptor beta gene
Jae Hee Lee, Eun Young Kim
Ann Pediatr Endocrinol Metab. 2014;19(4):229-231.   Published online December 31, 2014
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Turner syndrome masquerading as normal early puberty
Yong Hee Hong, Young Lim Shin
Ann Pediatr Endocrinol Metab. 2014;19(4):225-228.   Published online December 31, 2014
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Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family
Myo-Jing Kim, Young-Eun Kim, Chang-Seok Ki, Jae-Ho Yoo
Ann Pediatr Endocrinol Metab. 2014;19(4):220-224.   Published online December 31, 2014
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A case of thyrotoxic periodic paralysis as initial manifestation of Graves' disease in a 16-year-old Korean adolescent
Se Yong Jung, Kyung Chul Song, Jae Il Shin, Hyun Wook Chae, Ho-Seong Kim, Ah Reum Kwon
Ann Pediatr Endocrinol Metab. 2014;19(3):169-173.   Published online September 30, 2014
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Long-term follow-up on Cushing disease patient after transsphenoidal surgery
Insook Jeong, Moonyeon Oh, Ja Hye Kim, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2014;19(3):164-168.   Published online September 30, 2014
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Prepubertal unilateral gynecomastia in the absence of endocrine abnormalities
Min Kang, Chan Jae Lee, Il Tae Hwang, Kwanseop Lee, Min Jae Kang
Ann Pediatr Endocrinol Metab. 2014;19(3):159-163.   Published online September 30, 2014
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A 3-year-old girl with Graves' disease with literature review
Yo Han Ho, Eun Cho Chung, Sin-Ae Park
Ann Pediatr Endocrinol Metab. 2014;19(3):154-158.   Published online September 30, 2014
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A Korean boy with 46,XX testicular disorder of sex development caused by SOX9 duplication
Gyung Min Lee, Jung Min Ko, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab. 2014;19(2):108-112.   Published online June 30, 2014
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Refractory acute suppurative thyroiditis secondary to pyriform sinus fistula
Jee Hyue Seo, Yong Hoon Park, Sei Won Yang, Hyun Young Kim
Ann Pediatr Endocrinol Metab. 2014;19(2):104-107.   Published online June 30, 2014
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