Annals of Pediatric Endocrinology & Metabolism


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
Cited By 9; Full text PubReader ePub Crossref - TDM PDF


Short stature and growth hormone deficiency in a girl with encephalocraniocutaneous lipomatosis and Jaffe-Campanacci syndrome: a case report: Eun mi Choi, Nani Jung, Ye Jee Shim, Hee Joung Choi, Joon Sik Kim, Heung Sik Kim, Kwang Soon Song, Hee Jung Lee, Sang Pyo Kim; Ann Pediatr Endocrinol Metab. 2016;21(4):240-244. Published online December 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.4.240
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Multiple daily injection of insulin regimen for a 10-month-old infant with type 1 diabetes mellitus and diabetic ketoacidosis: Ji Hyun Park, So Young Shin, Ye Jee Shim, Jin Hyeok Choi, Heung Sik Kim; Ann Pediatr Endocrinol Metab. 2016;21(2):96-98. Published online June 30, 2016; DOI: https://doi.org/10.6065/apem.2016.21.2.96; Full text PubReader ePub Crossref - TDM PDF


Insulin and glucagon levels of umbilical cord blood in appropriate for gestational age - preterm infants with or without postnatal hypoglycemia: Jae Hyun Park, Jin Gon Bae, Shin Kim, Chun Soo Kim, Sang Lak Lee, Heung Sik Kim; Ann Pediatr Endocrinol Metab. 2016;21(2):86-91. Published online June 30, 2016; DOI: https://doi.org/10.6065/apem.2016.21.2.86
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Formula fed twin infants with recurrent hypocalcemic seizures with vitamin D deficient rickets and hyperphosphatemia: Byung Wook Jo, Ye Jee Shim, Jin Hyeok Choi, Jun Sik Kim, Hee Joung Lee, Heung Sik Kim; Ann Pediatr Endocrinol Metab. 2015;20(2):102-105. Published online June 30, 2015; DOI: https://doi.org/10.6065/apem.2015.20.2.102
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Familial hypobetalipoproteinemia: a novel mutation in APOB gene and review of the literature: So Yun Park, Heung Sik Kim, Mi Ae Chu, Hyo-Jeong Jang, Seokjin Kang; Received August 5, 2022 Accepted September 20, 2022; DOI: https://doi.org/10.6065/apem.2244180.090 [Accepted]; PDF

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