Annals of Pediatric Endocrinology & Metabolism


Update on the current modalities used to screen high risk youth for prediabetes and/or type 2 diabetes mellitus: Preneet Cheema Brar; Ann Pediatr Endocrinol Metab. 2019;24(2):71-77. Published online June 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.2.71
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A case of immune-mediated type 1 diabetes mellitus due to congenital rubella ınfection: Hüseyin Anıl Korkmaz, Çağatay Ermiş; Ann Pediatr Endocrinol Metab. 2019;24(1):68-70. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.68
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Infantile hypercalcemia with novel compound heterozygous mutation in SLC34A1 encoding renal sodium-phosphate cotransporter 2a: a case report: Seok Jin Kang, Rosie Lee, Heung Sik Kim; Ann Pediatr Endocrinol Metab. 2019;24(1):64-67. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.64
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A case of de novo 18p deletion syndrome with panhypopituitarism: Aram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2019;24(1):60-63. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.60
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Episodes of prolonged “trance-like state” in an infant with hypothalamic hamartoma: Rakesh Kumar, Jaivinder Yadav, Jitendra Kumar Sahu, Manjul Tripathi, Chirag Ahuja, Devi Dayal; Ann Pediatr Endocrinol Metab. 2019;24(1):55-59. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.55
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A novel CHD7 mutation in an adolescent presenting with growth and pubertal delay: Maria-Christina Antoniou, Thérèse Bouthors, Cheng Xu, Franziska Phan-Hug, Eglantine Elowe-Gruau, Sophie Stoppa-Vaucher, Almer van der Sloot, James Acierno, Daniele Cassatella, Celine Richard, Andrew Dwyer, Nelly Pitteloud, Michael Hauschild; Ann Pediatr Endocrinol Metab. 2019;24(1):49-54. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.49
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Risk assessment of metabolic syndrome in adolescents using the triglyceride/high-density lipoprotein cholesterol ratio and the total cholesterol/high-density lipoprotein cholesterol ratio: Shou-Yu Chu, Ji-Hyun Jung, Mi-Jung Park, Shin-Hye Kim; Ann Pediatr Endocrinol Metab. 2019;24(1):41-48. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.41
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Reference range of random urinary calcium creatinine ratio in North Indian children and adolescents: Raman Kumar Marwaha, Mahendra Kumar Garg, Navin Dang, Ambrish Mithal, Archna Narang, Aditi Chadha, Nandita Gupta, Manchanda Raj Kumar; Ann Pediatr Endocrinol Metab. 2019;24(1):34-40. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.34
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Morning basal luteinizing hormone, a good screening tool for diagnosing central precocious puberty: Dong-Min Lee, In-Hyuk Chung; Ann Pediatr Endocrinol Metab. 2019;24(1):27-33. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.27
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Response to vitamin D replacement in overweight and normal weight children with vitamin D deficiency: In Hyuk Chung, Yu Sun Kang, Eun-Gyong Yoo; Ann Pediatr Endocrinol Metab. 2019;24(1):22-26. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.22
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Screening and management of thyroid dysfunction in preterm infants: Hye Rim Chung; Ann Pediatr Endocrinol Metab. 2019;24(1):15-21. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.15
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Genetic regulation of linear growth: Shanna Yue, Philip Whalen, Youn Hee Jee; Ann Pediatr Endocrinol Metab. 2019;24(1):2-14. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.2
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Annals of Pediatric Endocrinology & Metabolism is now indexed in the Emerging Sources Citation Index: Ji-Eun Lee; Ann Pediatr Endocrinol Metab. 2019;24(1):1-1. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.1; Full text PubReader ePub PDF


Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene: Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh; Ann Pediatr Endocrinol Metab. 2018;23(4):235-239. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.235
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A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets: Misun Yang, Jinsup Kim, Aram Yang, Jahyun Jang, Tae Yeon Jeon, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2018;23(4):229-234. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.229
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