Annals of Pediatric Endocrinology & Metabolism

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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; DOI: https://doi.org/10.6065/apem.2018.23.1.51
Web of Science 4 Crossref 5; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2017.22.4.266
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Clinical course of infants with congenital heart disease who developed thyroid dysfunction within 100 days: Hye Jin Lee, Hyeoh Won Yu, Gi Beom Kim, Choong Ho Shin, Sei Won Yang, Young Ah Lee; Ann Pediatr Endocrinol Metab. 2017;22(4):253-258. Published online December 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.4.253
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Development of disease-specific growth charts in Turner syndrome and Noonan syndrome: Tsuyoshi Isojima, Susumu Yokoya; Ann Pediatr Endocrinol Metab. 2017;22(4):240-246. Published online December 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.4.240
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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; DOI: https://doi.org/10.6065/apem.2017.22.3.208
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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; DOI: https://doi.org/10.6065/apem.2017.22.3.203
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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; DOI: https://doi.org/10.6065/apem.2017.22.3.197
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Nonalcoholic fatty liver disease in long-term survivors of childhood-onset craniopharyngioma: So Yoon Jung, Yun Jeong Lee, Hye Jin Lee, Young Ah Lee, Jin Soo Moon, Jae Sung Ko, Sei Won Yang, Choong Ho Shin; Ann Pediatr Endocrinol Metab. 2017;22(3):189-196. Published online September 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.3.189
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Impact of targeted education on managing warning and error signals by children and adolescents with type 1 diabetes using the Accu-Chek Combo Insulin Pump System: Asma Deeb, Nabras Al Qahtani, Amal Al Ali, Mariette Akle; Ann Pediatr Endocrinol Metab. 2017;22(3):170-175. Published online September 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.3.170
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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; DOI: https://doi.org/10.6065/apem.2017.22.2.133
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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; DOI: https://doi.org/10.6065/apem.2017.22.2.129
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Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders: Maki Fukami, Mami Miyado; Ann Pediatr Endocrinol Metab. 2017;22(2):90-94. Published online June 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.2.90
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The rapid internationalization of Annals of Pediatric Endocrinology & Metabolism as evidenced by journal metrics: Sun Huh; Ann Pediatr Endocrinol Metab. 2017;22(2):77-81. Published online June 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.2.77
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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; DOI: https://doi.org/10.6065/apem.2017.22.1.65
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Growth without growth hormone in combined pituitary hormone deficiency caused by pituitary stalk interruption syndrome: Sang Soo Lee, A-Leum Han, Moon Bae Ahn, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung-Kyu Suh; Ann Pediatr Endocrinol Metab. 2017;22(1):55-59. Published online March 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.1.55
Web of Science 12 Crossref 10; Full text PubReader ePub PDF

Journal Impact Factor 2.8

Pediatrics Q1

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