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Review Articles
- Exosomes as the source of biomarkers of metabolic diseases
- Min-Jae Lee, Dong-Ho Park, Ju-Hee Kang
- Ann Pediatr Endocrinol Metab. 2016;21(3):119-125. Published online September 30, 2016
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- Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
- Chong Kun Cheon
- Ann Pediatr Endocrinol Metab. 2016;21(3):126-135. Published online September 30, 2016
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Original Articles
- Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty
- Eungu Kang, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo
- Ann Pediatr Endocrinol Metab. 2016;21(3):136-142. Published online September 30, 2016
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- The cutoff values of indirect indices for measuring insulin resistance for metabolic syndrome in Korean children and adolescents
- Jun Woo Kim, Sang Hoo Park, Yoojin Kim, Minji Im, Heon-Seok Han
- Ann Pediatr Endocrinol Metab. 2016;21(3):143-148. Published online September 30, 2016
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- Vitamin D deficiency in children aged 6 to 12 years: single center's experience in Busan
- Young Eun Roh, Bo Ryung Kim, Won Bok Choi, Young Mi Kim, Min-Jung Cho, Hye-Young Kim, Kyung Hee Park, Kwang Hoon Kim, Peter Chun, Su Young Kim, Min Jung Kwak
- Ann Pediatr Endocrinol Metab. 2016;21(3):149-154. Published online September 30, 2016
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- Body image and depression in girls with idiopathic precocious puberty treated with gonadotropin-releasing hormone analogue
- Min-Seon Choi, Eun-Young Kim
- Ann Pediatr Endocrinol Metab. 2016;21(3):155-160. Published online September 30, 2016
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Case Reports
- A baby with congenital hypothyroidism born to a hypothyroid mother who expressed undiagnosed thyroid stimulation blocking antibody
- Mock Ryeon Kim, Hye Won Park, Sochung Chung
- Ann Pediatr Endocrinol Metab. 2016;21(3):161-163. Published online September 30, 2016
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- Diagnostic difficulties by the unusual presentations in children and adolescents with Hashimoto thyroiditis
- Betül Ersoy, Kiremitçi Yılmaz Seniha, Deniz Kızılay, Münevver Yılmaz, Şenol Coşkun
- Ann Pediatr Endocrinol Metab. 2016;21(3):164-168. Published online September 30, 2016
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- Long-term clinical outcome and the identification of homozygous
CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A - Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
- Ann Pediatr Endocrinol Metab. 2016;21(3):169-173. Published online September 30, 2016
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- Endocrine complications during and after adolescence in a patient with cystinosis
- Moon Bae Ahn, Sung Eun Kim, Won Kyoung Cho, Min Ho Jung, Byung Kyu Suh
- Ann Pediatr Endocrinol Metab. 2016;21(3):174-178. Published online September 30, 2016
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Retraction Notice from Journal Editor
- Retraction: Mixed gonadal dysgenesis in 45,X Turner syndrome with
SRY gene - Ann Pediatr Endocrinol Metab. 2016;21(3):179-179. Published online September 30, 2016
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