Annals of Pediatric Endocrinology & Metabolism


Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita: Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Kyung Chul Song, Jin-Sung Lee, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2021;26(2):126-129. Published online June 30, 2021; DOI: https://doi.org/10.6065/apem.2040088.044
Web of Science 2 Crossref 2; Full text PubReader ePub PDF


Transcriptional coordination of hepatic autophagy by nutrient-sensing nuclear receptor PPARα and FXR: Jae Man Lee; Ann Pediatr Endocrinol Metab. 2016;21(4):193-198. Published online December 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.4.193
Crossref 19; Full text PubReader ePub PDF


Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome: Ji Won Koh, So Young Kang, Gu Hwan Kim, Han Wook Yoo, Jeesuk Yu; Ann Pediatr Endocrinol Metab. 2013;18(2):90-94. Published online June 30, 2013; DOI: https://doi.org/10.6065/apem.2013.18.2.90
Crossref 11; Full text PubReader ePub PDF

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