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Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia
Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani
Ann Pediatr Endocrinol Metab. 2018;23(3):1-4.   Published online September 28, 2018
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De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidism
Jung-Eun Moon, Su-Jeong Lee, Suk-Hyun Park, Jinsup Kim, Dong-Kyu Jin, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2018;23(2):107-111.   Published online June 20, 2018
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Respiratory failure in a diabetic ketoacidosis patient with severe hypophosphatemia
Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2018;23(2):103-106.   Published online June 20, 2018
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Association Kikuchi disease with Hashimoto thyroiditis: a case report and literature review
Eun Joo Lee, Hae Sang Lee, Jun Eun Park, Jin Soon Hwang
Ann Pediatr Endocrinol Metab. 2018;23(2):99-102.   Published online June 20, 2018
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Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report
Dai Jung, Go Hun Seo, Yoon-Myung Kim, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2018;23(1):51-55.   Published online March 22, 2018
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Congenital hyperinsulinism: diagnostic and management challenges in a developing country – case report
Cheri Mathews John, Prakash Agarwal, Suriyakumar Govindarajulu, Sandhya Sundaram, Senthil Senniappan
Ann Pediatr Endocrinol Metab. 2017;22(4):272-275.   Published online December 31, 2017
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A boy with 46,X,+mar presenting gynecomastia and short stature
Ki Eun Kim, Ye Jin Kim, Mo Kyoung Jung, Hyun-Wook Chae, Ah Reum Kwon, Woo Jung Lee, Duk-Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(4):266-271.   Published online December 31, 2017
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Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency
Kyung Mi Jang, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2017;22(3):208-212.   Published online September 28, 2017
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An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing
Jinsup Kim, Sung Yoon Cho, Aram Yang, Ja-Hyun Jang, Youngbin Choi, Ji-Eun Lee, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(3):203-207.   Published online September 28, 2017
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A rare case of multiple pituitary adenomas in an adolescent Cushing disease presenting as a vertebral compression fracture
Ji-Yeon Song, Sue-Jean Mun, Soon-Ki Sung, Jae-Yeon Hwang, Seung-Kug Baik, Jee Yeon Kim, Chong-Kun Cheon, Su-Young Kim, Yoo-Mi Kim
Ann Pediatr Endocrinol Metab. 2017;22(3):197-202.   Published online September 28, 2017
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Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus
Dong-Yoon Yoo, Hae Jung Kim, Kee Hyun Cho, Eun Byul Kwon, Eun-Gyong Yoo
Ann Pediatr Endocrinol Metab. 2017;22(2):133-138.   Published online June 28, 2017
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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(2):129-132.   Published online June 28, 2017
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Diabetes mellitus due to agenesis of the dorsal pancreas in a patient with heterotaxy syndrome
Jo Eun Jung, Jin Ho Hur, Mo Kyung Jung, Ahreum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(2):125-128.   Published online June 28, 2017
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A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
Mo Kyung Jung, Juhyun Jin, Hyun Ok Kim, Ahreum Kwon, Hyun Wook Chae, Seok Jin Kang, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(1):68-71.   Published online March 31, 2017
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A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome
Devi Dayal, Dinesh Giri, Senthil Senniappan
Ann Pediatr Endocrinol Metab. 2017;22(1):65-67.   Published online March 31, 2017
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