Annals of Pediatric Endocrinology & Metabolism

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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes: Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie; Ann Pediatr Endocrinol Metab. 2015;20(4):230-234. Published online December 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.4.230
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene: Jae Yeop Jung, Sohyoung Yang, Eun-Hwan Jeong, Ho-Chang Lee, Yong-Moon Lee, Heon-Seok Han, Kyung Hee Yi; Ann Pediatr Endocrinol Metab. 2015;20(4):226-229. Published online December 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.4.226
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Cerebral salt-wasting syndrome after hematopoietic stem cell transplantation in adolescents: 3 case reports: Yeon Jin Jeon, Hyun Young Lee, In Ah Jung, Won-Kyoung Cho, Bin Cho, Byung-Kyu Suh; Ann Pediatr Endocrinol Metab. 2015;20(4):220-225. Published online December 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.4.220
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


XYY syndrome: a 13-year-old boy with tall stature: Won Ha Jo, Mo Kyung Jung, Ki Eun Kim, Hyun Wook Chae, Duk Hee Kim, Ah Reum Kwon, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2015;20(3):170-173. Published online September 30, 2015; DOI: https://doi.org/10.6065/apem.2015.20.3.170
Cited By 8; Full text PubReader ePub Crossref - TDM PDF


Hypotonic hyponatremia by primary polydipsia caused brain death in a 10-year-old boy: A Ra Ko, Soo Jung Kim, Mo Kyung Jung, Ki Eun Kim, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim, Ah Reum Kwon; Ann Pediatr Endocrinol Metab. 2015;20(3):166-169. Published online September 30, 2015; DOI: https://doi.org/10.6065/apem.2015.20.3.166
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.3.162
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.2.110
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.2.106
Cited By 8; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.2.102
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.2.98
Cited By 2; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.1.59
Cited By 10; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2014.19.4.229
Cited By 10; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2014.19.4.225
Cited By 7; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2014.19.4.220
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


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; DOI: https://doi.org/10.6065/apem.2014.19.3.169
Cited By 4; Full text PubReader ePub Crossref - TDM PDF

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