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Volume 25(1); Mar 2020
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Bone morbidity in pediatric acute lymphoblastic leukemia
Moon Bae Ahn, Byung-Kyu Suh
Ann Pediatr Endocrinol Metab.
2020;25(1):1-9.
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Updates on bone health in children with gastrointestinal diseases
Hye Ran Yang
Ann Pediatr Endocrinol Metab.
2020;25(1):10-14.
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Bone health in pediatric patients with neurological disorders
Ara Ko, Juhyun Kong, Furkat Samadov, Akmal Mukhamedov, Young Mi Kim, Yun-Jin Lee, Sang Ook Nam
Ann Pediatr Endocrinol Metab.
2020;25(1):15-23.
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Relationship between final adult height and birth weight after gonadotropin-releasing hormone agonist treatment in girls with central precocious puberty
Ah Young Cho, Su Yeong Ko, Jae Hee Lee, Eun Young Kim
Ann Pediatr Endocrinol Metab.
2020;25(1):24-30.
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Effect of -202 A/C IGFBP-3 polymorphisms on growth responses in children with idiopathic short stature
Hye Ree Kang, Il Tae Hwang, Seung Yang
Ann Pediatr Endocrinol Metab.
2020;25(1):31-37.
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Comparison of proinsulin to C-peptide ratio in children with and without type 1 diabetes and its relation to age
Benjamin R. Ellison, Jeffrey H. Burton, Daniel S. Hsia
Ann Pediatr Endocrinol Metab.
2020;25(1):38-41.
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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.
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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.
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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.
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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.
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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.
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