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Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disorders
Yoko Kuroki, Atsushi Hattori, Keiko Matsubara, Maki Fukami
Ann Pediatr Endocrinol Metab. 2024;29(3):156-160.   Published online June 30, 2024
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Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience
Su Jin Kim, Eunyoung Joo, Jisun Park, Chang Ahn Seol, Ji-Eun Lee
Ann Pediatr Endocrinol Metab. 2024;29(1):38-45.   Published online February 29, 2024
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A Korean male with Kleefstra syndrome presented with micropenis
Rosie Lee, Mi-seon Lee, Jung Eun Moon
Ann Pediatr Endocrinol Metab. 2023;28(4):308-311.   Published online December 31, 2023
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Denosumab use in osteogenesis imperfecta: an update on therapeutic approaches
Fatma Majdoub, Hanene Lassoued Ferjani, Dorra Ben Nessib, Dhia Kaffel, Kaouther Maatallah, Wafa Hamdi
Ann Pediatr Endocrinol Metab. 2023;28(2):98-106.   Published online June 30, 2023
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Wilson disease diagnosed incidentally by targeted gene panel sequencing in a Korean boy with severe obesity
Minji Im, Ari Song, Jiyeon Kim, Min-Sun Kim, Sae-Mi Lee, Mi Jin Kim, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2022;27(3):229-235.   Published online October 18, 2021
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Genetic obesity: an update with emerging therapeutic approaches
Young Bae Sohn
Ann Pediatr Endocrinol Metab. 2022;27(3):169-175.   Published online September 30, 2022
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Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
Teresa Nieto, Beatriz Castillo, Jacobo Nieto, Maria J. Redondo
Ann Pediatr Endocrinol Metab. 2022;27(2):121-125.   Published online October 12, 2021
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Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta
Yunha Choi, Soojin Hwang, Gu-Hwan Kim, Beom Hee Lee, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2022;27(1):22-29.   Published online January 25, 2022
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Balanced assessment of growth disorders using clinical, endocrinological, and genetic approaches
Martin Oswald Savage, Helen Louise Storr
Ann Pediatr Endocrinol Metab. 2021;26(4):218-226.   Published online December 31, 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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Thyroid imaging study in children with suspected thyroid dysgenesis
Sangwoo Chun, Young Seok Lee, Jeesuk Yu
Ann Pediatr Endocrinol Metab. 2021;26(1):53-59.   Published online March 31, 2021
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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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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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Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis
Yoon Myung Kim, Arum Oh, Kun-Suk Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2019;24(4):231-236.   Published online December 31, 2019
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