Annals of Pediatric Endocrinology & Metabolism

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An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism: Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Min-Hyun Cho, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2020;25(2):132-136. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938074.037; Full text PubReader ePub Crossref - TDM PDF


Effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome: Hyun Woo Son, Jeong Eun Lee, Seung Hwan Oh, Changwon Keum, Woo Yeong Chung; Ann Pediatr Endocrinol Metab. 2020;25(2):126-131. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938144.072
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Body fat composition and miR-378 expression profiling in patients with type 1 diabetes: Lissette Duarte, Diego F. García-Díaz, Francisco Pérez-Bravo; Ann Pediatr Endocrinol Metab. 2020;25(2):118-125. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938088.044
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption: Sae Bit Yu, Yena Lee, Arum Oh, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2020;25(2):112-117. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938142.071
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Serum uric acid in Korean children and adolescents: reference percentiles and association with metabolic syndrome: Myung Hyun Cho, Yoon Mo Kim, Jong Hyung Yoon, Dong Ho Kim, Jung Sub Lim; Ann Pediatr Endocrinol Metab. 2020;25(2):104-111. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938156.078
Cited By 10; Full text PubReader ePub Crossref - TDM PDF Supplementary Material


Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency: Yena Lee, Jin-Ho Choi, Arum Oh, Gu-Hwan Kim, Sook-Hyun Park, Jung Eun Moon, Cheol Woo Ko, Chong-Kun Cheon, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2020;25(2):97-103. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938152.076
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


Prevalence of idiopathic scoliosis in girls with central precocious puberty: effect of a gonadotropin-releasing hormone agonist: Lindsey Yoojin Chung, Hyo-Kyoung Nam, Young-Jun Rhie, Rimm Huh, Kee-Hyoung Lee; Ann Pediatr Endocrinol Metab. 2020;25(2):92-96. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938164.082
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Minipuberty of human infancy – A window of opportunity to evaluate hypogonadism and differences of sex development?: Christoffer Højrup Renault, Lise Aksglaede, Ditte Wøjdemann, Anna Berg Hansen, Rikke Beck Jensen, Anders Juul; Ann Pediatr Endocrinol Metab. 2020;25(2):84-91. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.2040094.047
Cited By 16; Full text PubReader ePub Crossref - TDM PDF


Eating speed and the risk of type 2 diabetes: explorations based on real-world evidence: Sai Krishna Gudi; Ann Pediatr Endocrinol Metab. 2020;25(2):80-83. Published online April 22, 2020; DOI: https://doi.org/10.6065/apem.2040028.014
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


Deciphering short stature in children: Nella Polidori, Valeria Castorani, Angelika Mohn, Francesco Chiarelli; Ann Pediatr Endocrinol Metab. 2020;25(2):69-79. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.2040064.032
Cited By 19; Full text PubReader ePub Crossref - TDM PDF


Identification of a novel variant in the PHEX gene using targeted gene panel sequencing in a 24-month-old boy with hypophosphatemic rickets: Ha Young Jo, Jung Hyun Shin, Hye Young Kim, Young Mi Kim, Heirim Lee, Mi Hye Bae, Kyung Hee Park, Ja-Hyun Jang, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2020;25(1):63-67. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.63
Cited By 2; Full text PubReader ePub Crossref - TDM PDF


Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene: So Yoon Jung, Jeongho Lee, Dong Hwan Lee; Ann Pediatr Endocrinol Metab. 2020;25(1):57-62. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.57
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Successful rapid weight reduction and the use of liraglutide for morbid obesity in adolescent Prader-Willi syndrome: Yoo-Mi Kim, Yeoun Joo Lee, Soo Yeon Kim, Chong Kun Cheon, Han Hyuk Lim; Ann Pediatr Endocrinol Metab. 2020;25(1):52-56. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.52
Cited By 19; Full text PubReader ePub Crossref - TDM PDF


Nonclassic congenital lipoid adrenal hyperplasia diagnosed at 17 months in a Korean boy with normal male genitalia: emphasis on pigmentation as a diagnostic clue: Hosun Bae, Min-Sun Kim, Hyojung Park, Ja-Hyun Jang, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2020;25(1):46-51. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.46
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families: Adnan Al Shaikh, Bader Shirah, Somaya Alzelaye; Ann Pediatr Endocrinol Metab. 2020;25(1):42-45. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.42
Cited By 5; Full text PubReader ePub Crossref - TDM PDF

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