| 119 |
Exosomes as the source of biomarkers of metabolic diseasesExosomes as the source of biomarkers of metabolic diseases
Min-Jae Lee, Dong-Ho Park, Ju-Hee KangMin-Jae Lee, Dong-Ho Park, Ju-Hee Kang
KMSID: 1516085184 Ann Pediatr Endocrinol Metab. 2016;21(3):119-125. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.119 |
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| 126 |
Genetics of Prader-Willi syndrome and Prader-Will-Like syndromeGenetics of Prader-Willi syndrome and Prader-Will-Like syndrome
Chong Kun CheonChong Kun Cheon
KMSID: 1516085185 Ann Pediatr Endocrinol Metab. 2016;21(3):126-135. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.126 |
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| 136 |
Etiology and therapeutic outcomes of children with gonadotropin-independent precocious pubertyEtiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty
Eungu Kang, Ja Hyang Cho, Jin-Ho Choi, Han-Wook YooEungu Kang, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo
KMSID: 1516085186 Ann Pediatr Endocrinol Metab. 2016;21(3):136-142. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.136 |
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| 143 |
The cutoff values of indirect indices for measuring insulin resistance for metabolic syndrome in Korean children and adolescentsThe 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 HanJun Woo Kim, Sang Hoo Park, Yoojin Kim, Minji Im, Heon-Seok Han
KMSID: 1516085187 Ann Pediatr Endocrinol Metab. 2016;21(3):143-148. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.143 |
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| 149 |
Vitamin D deficiency in children aged 6 to 12 years: single center's experience in BusanVitamin 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 KwakYoung 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
KMSID: 1516085192 Ann Pediatr Endocrinol Metab. 2016;21(3):149-154. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.149 |
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| 155 |
Body image and depression in girls with idiopathic precocious puberty treated with gonadotropin-releasing hormone analogueBody image and depression in girls with idiopathic precocious puberty treated with gonadotropin-releasing hormone analogue
Min-Seon Choi, Eun-Young KimMin-Seon Choi, Eun-Young Kim
KMSID: 1516085191 Ann Pediatr Endocrinol Metab. 2016;21(3):155-160. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.155 |
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| 161 |
A baby with congenital hypothyroidism born to a hypothyroid mother who expressed undiagnosed thyroid stimulation blocking antibodyA baby with congenital hypothyroidism born to a hypothyroid mother who expressed undiagnosed thyroid stimulation blocking antibody
Mock Ryeon Kim, Hye Won Park, Sochung ChungMock Ryeon Kim, Hye Won Park, Sochung Chung
KMSID: 1516085189 Ann Pediatr Endocrinol Metab. 2016;21(3):161-163. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.161 |
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| 164 |
Diagnostic difficulties by the unusual presentations in children and adolescents with Hashimoto thyroiditisDiagnostic difficulties by the unusual presentations in children and adolescents with Hashimoto thyroiditis
Betül Ersoy, Kiremitçi Yılmaz Seniha, Deniz Kızılay, Münevver Yılmaz, Şenol CoşkunBetül Ersoy, Kiremitçi Yılmaz Seniha, Deniz Kızılay, Münevver Yılmaz, Şenol Coşkun
KMSID: 1516085188 Ann Pediatr Endocrinol Metab. 2016;21(3):164-168. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.164 |
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| 169 |
Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1ALong-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 YooJa Hyang Cho, Eungu Kang, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
KMSID: 1516085193 Ann Pediatr Endocrinol Metab. 2016;21(3):169-173. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.169 |
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| 174 |
Endocrine complications during and after adolescence in a patient with cystinosisEndocrine complications during and after adolescence in a patient with cystinosis
Moon Bae Ahn, Sung Eun Kim, Won Kyoung Cho, Min Ho Jung, Byung Kyu SuhMoon Bae Ahn, Sung Eun Kim, Won Kyoung Cho, Min Ho Jung, Byung Kyu Suh
KMSID: 1516085195 Ann Pediatr Endocrinol Metab. 2016;21(3):174-178. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.174 |
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| 179 |
Retraction: Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY geneRetraction: Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
KMSID: 1516085194 Ann Pediatr Endocrinol Metab. 2016;21(3):179-179. Published online 2016 September 30 DOI: http://dx.doi.org/10.6065/apem.2016.21.3.179 |
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