Annals of Pediatric Endocrinology & Metabolism

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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
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


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 11; Full text PubReader ePub Crossref - TDM PDF


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
Cited By 7; Full text PubReader ePub Crossref - TDM PDF Supplementary Material


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
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


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
Cited By 4; Full text PubReader ePub Crossref - TDM 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
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


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
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia: Eun Mi Cho, Jung Eun Moon, Soo Jung Lee, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2018;23(4):226-228. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.226
Cited By 8; Full text PubReader ePub Crossref - TDM PDF


Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy: You Jung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Sei Won Yang, Man Jin Kim, Sung Sub Park; Ann Pediatr Endocrinol Metab. 2018;23(4):220-225. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.220
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita: Anastasios Serbis, Vassiliki Regina Tsinopoulou, Konstantina Mouzaki, Eleni P. Kotanidou, Styliani Giza, Assimina Galli-Tsinopoulou; Ann Pediatr Endocrinol Metab. 2018;23(3):162-165. Published online September 28, 2018; DOI: https://doi.org/10.6065/apem.2018.23.3.162
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia: Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani; Ann Pediatr Endocrinol Metab. 2018;23(3):158-161. Published online September 28, 2018; DOI: https://doi.org/10.6065/apem.2018.23.3.158
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11: Jong Seo Yoon, Kyu Jung Park, Young Bae Sohn, Hae Sang Lee, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2018;23(3):154-157. Published online September 28, 2018; DOI: https://doi.org/10.6065/apem.2018.23.3.154
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidism: Jung-Eun Moon, Su-Jeong Lee, Suk-Hyun Park, Jinsup Kim, Dong-Kyu Jin, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2018;23(2):107-111. Published online June 20, 2018; DOI: https://doi.org/10.6065/apem.2018.23.2.107
Cited By 5; Full text PubReader ePub Crossref - TDM PDF


Respiratory failure in a diabetic ketoacidosis patient with severe hypophosphatemia: Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Duk Hee Kim, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2018;23(2):103-106. Published online June 20, 2018; DOI: https://doi.org/10.6065/apem.2018.23.2.103
Cited By 15; Full text PubReader ePub Crossref - TDM PDF


Association Kikuchi disease with Hashimoto thyroiditis: a case report and literature review: Eun Joo Lee, Hae Sang Lee, Jun Eun Park, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2018;23(2):99-102. Published online June 20, 2018; DOI: https://doi.org/10.6065/apem.2018.23.2.99
Cited By 10; Full text PubReader ePub Crossref - TDM PDF

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