Previous Issue   Volume 23(4); Dec 2018
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Issues
Clinical genetics of defects in thyroid hormone synthesis
Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2018;23(4):169-175.
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Growth hormone therapy in patients with Noonan syndrome
Go Hun Seo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2018;23(4):176-181.
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Early-life exposure to endocrine disrupting chemicals associates with childhood obesity
Chunxue Yang, Hin Kiu Lee, Alice Pik Shan Kong, Lee Ling Lim, Zongwei Cai, Arthur C.K. Chung
Ann Pediatr Endocrinol Metab. 2018;23(4):182-195.
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Association between hemoglobin glycation index and cardiometabolic risk factors in Korean pediatric nondiabetic population
Bora Lee, You Jung Heo, Young Ah Lee, Jieun Lee, Jae Hyun Kim, Seong Yong Lee, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab. 2018;23(4):196-203.
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The role of p21/CIP1/WAF1 (p21) in the negative regulation of the growth hormone/growth hormone receptor and epidermal growth factor/epidermal growth factor receptor pathways, in growth hormone transduction defect
Eirini Kostopoulou, Andrea Paola Rojas Gil, Bessie E. Spiliotis
Ann Pediatr Endocrinol Metab. 2018;23(4):204-209.
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Interpretation of androgen and anti-Mullerian hormone profiles in a Hispanic cohort of 5- to 8-year-old girls with premature adrenarche
Preneet Cheema Brar, Elena Dingle, Daniela Ovadia, Sarah Pivo, Veeramac Prasad, Raphael David
Ann Pediatr Endocrinol Metab. 2018;23(4):210-214.
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The effect of overweight on the luteinizing hormone level after gonadorelin stimulation test in girls with idiopathic central precocious puberty
Hyun Young Lee, Yoon-Ji Lee, Moon-Bae Ahn, Won-Kyoung Cho, Byung-Kyu Suh
Ann Pediatr Endocrinol Metab. 2018;23(4):215-219.
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Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy
You Jung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Sei Won Yang, Man Jin Kim, Sung Sub Park
Ann Pediatr Endocrinol Metab. 2018;23(4):220-225.
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Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia
Eun Mi Cho, Jung Eun Moon, Soo Jung Lee, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2018;23(4):226-228.
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A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets
Misun Yang, Jinsup Kim, Aram Yang, Jahyun Jang, Tae Yeon Jeon, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2018;23(4):229-234.
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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh
Ann Pediatr Endocrinol Metab. 2018;23(4):235-239.
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