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Volume 21(3); Sep 2016
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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Retraction: Mixed gonadal dysgenesis in 45,X Turner syndrome with
SRY
gene
Ann Pediatr Endocrinol Metab.
2016;21(3):179-179.
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