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Hypoparathyroidism in children and adolescents
Hüseyin Anıl Korkmaz, Behzat Ozkan
Ann Pediatr Endocrinol Metab. 2023;28(3):159-167.   Published online September 19, 2023
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Risk factors of postoperative hypoparathyroidism after total thyroidectomy in pediatric patients with thyroid cancer
Yunsoo Choe, Yun Jeong Lee, Choong Ho Shin, Eun-Jae Chung, Young Ah Lee
Ann Pediatr Endocrinol Metab. 2023;28(1):26-33.   Published online June 28, 2022
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A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe)
Jung Eun Moon, Hee-Young Yang, Gabbine Wee, Suk-Hyun ParK, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2021;26(1):24-30.   Published online July 30, 2020
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Primary hyperparathyroidism versus familial hypocalciuric hypercalcemia: a challenging diagnostic evaluation in an adolescent female
Mustafa Tosur, Monica E. Lopez, David L. Paul
Ann Pediatr Endocrinol Metab. 2019;24(3):195-198.   Published online September 30, 2019
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A case of vitamin D hydroxylation-deficient rickets type 1A caused by 2 novel pathogenic variants in CYP27B1 gene
You-Min Kim, Yoon-Young Jang, Ji-Eun Jeong, Hye-Jin Park, Ja-Hyun Jang, Jin-Kyung Kim
Ann Pediatr Endocrinol Metab. 2019;24(2):137-141.   Published online June 30, 2019
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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
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Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus
Dong-Yoon Yoo, Hae Jung Kim, Kee Hyun Cho, Eun Byul Kwon, Eun-Gyong Yoo
Ann Pediatr Endocrinol Metab. 2017;22(2):133-138.   Published online June 28, 2017
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Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A
Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(3):169-173.   Published online September 30, 2016
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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
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Clinical and laboratory characteristics of neonatal hypocalcemia
Won Im Cho, Hyeoh Won Yu, Hye Rim Chung, Choong Ho Shin, Sei Won Yang, Chang Won Choi, Beyong Il Kim
Ann Pediatr Endocrinol Metab. 2015;20(2):86-91.   Published online June 30, 2015
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Proton-Pump Inhibitor-Induced Hypocalcemia and Hypomagnesemia.
Sae Rom Choi, Jung Hee Byun, Ah Reum Kwon, Ye Jin Kim, Yong Hyuk Kim, Hyun Wook Chae, Ho Seong Kim
Ann Pediatr Endocrinol Metab. 2012;17(4):249-252.
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A Case of Idiopathic Hypomagnesemia with Hypocalcemia Presenting as Generalized Tonic-Clonic Seizure.
Seul Lee, Ah Reum Kwon, Hyun Wook Chae, Ho Seong Kim
Ann Pediatr Endocrinol Metab. 2011;16(3):193-195.
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A Case of Hypocalcemia due to Vitamin D Deficiency in Exclusively Breast-fed Infant.
Su Nam Bae, Eui Jung Rho, Jae Woo Lim, Eun Jung Cheon, Kyong Og Ko, Young Hyuk Lee
Ann Pediatr Endocrinol Metab. 2006;11(2):205-208.
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The Endocrine Manifestations and Growth of the Patients with 22q11.2 Microdeletion Syndrome.
Jong Seung Lee, Jin Ho Choi, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2004;9(1):66-71.
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