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Myhre syndrome: the first case in Korea
Dongjin Lim, Jae Hyun Kim, Jieun Lee
Ann Pediatr Endocrinol Metab. 2021;26(3):210-214.   Published online May 12, 2021
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Immobilization-induced symptomatic hypercalcemia treated with zoledronate in a child with a left ventricular assist device
Emrah Gün, Tanıl Kendirli, Edin Botan, Tayfun Uçar, Zehra Aycan, Ahmet Rüçhan Akar
Ann Pediatr Endocrinol Metab. 2021;26(3):205-209.   Published online May 12, 2021
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A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets
In Hwa Jeong, Jae-Ho Yoo, Namhee Kim
Ann Pediatr Endocrinol Metab. 2021;26(2):130-133.   Published online June 30, 2021
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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
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Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2021;26(1):66-70.   Published online March 31, 2021
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Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8
Julie Mouron-Hryciuk, Sophie Stoppa-Vaucher, Kanetee Busiah, Thérèse Bouthors, Maria Christina Antoniou, Eric Jacot, Klaus Brusgaard, Henrik Thybo Christesen, Khalid Hussain, Andrew Dwyer, Matthias Roth-Kleiner, Michael Hauschild
Ann Pediatr Endocrinol Metab. 2021;26(1):60-65.   Published online August 7, 2020
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An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial nonautoimmune hyperthyroidism
Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2020;25(4):282-286.   Published online December 31, 2020
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Cushing syndrome with acute kidney injury due to ureteral stones in a 6-year-old boy
Kyungchul Song, Ahreum Kwon, Junghwan Suh, Han Saem Choi, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2020;25(4):277-281.   Published online August 7, 2020
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Identification of a heterozygous ACAN mutation in a 15-year-old boy with short stature who presented with advanced bone age: a case report and review of the literature
Tae Youp Kim, Kyung Mi Jang, Chang Won Keum, Seung Hwan Oh, Woo Yeong Chung
Ann Pediatr Endocrinol Metab. 2020;25(4):272-276.   Published online July 29, 2020
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Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an FGFR1 gene variant
Jaewon Choe, Jae Hyun Kim, Young Ah Kim, Jieun Lee
Ann Pediatr Endocrinol Metab. 2020;25(3):192-197.   Published online July 29, 2020
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A case of primary hyperparathyroidism due to an intrathymic ectopic parathyroid adenoma in a 15-year-old boy
Youngseok Seo, Kyungchul Song, Han Saem Choi, Junghwan Suh, Ahreum Kwon, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2020;25(3):187-191.   Published online July 29, 2020
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An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism
Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Min-Hyun Cho, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2020;25(2):132-136.   Published online June 30, 2020
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Effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome
Hyun Woo Son, Jeong Eun Lee, Seung Hwan Oh, Changwon Keum, Woo Yeong Chung
Ann Pediatr Endocrinol Metab. 2020;25(2):126-131.   Published online June 30, 2020
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Identification of a novel variant in the PHEX gene using targeted gene panel sequencing in a 24-month-old boy with hypophosphatemic rickets
Ha Young Jo, Jung Hyun Shin, Hye Young Kim, Young Mi Kim, Heirim Lee, Mi Hye Bae, Kyung Hee Park, Ja-Hyun Jang, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2020;25(1):63-67.   Published online March 31, 2020
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Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene
So Yoon Jung, Jeongho Lee, Dong Hwan Lee
Ann Pediatr Endocrinol Metab. 2020;25(1):57-62.   Published online March 31, 2020
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