Improving the lives of children with neurofibromatosis type 1 by Yoo-Mi Kim

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Comparison of anthropometric, metabolic, and body compositional abnormalities in Korean children and adolescents born small, appropriate, and large for gestational age: a populatio... by Tae Kwan Lee, Yoo Mi Kim, Han Hyuk Lim

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Single random measurement of urinary gonadotropin concentration for screening and monitoring girls with central precocious puberty by Se Young Lee, Ji Myung Kim, Yoo Mi Kim, Han Hyuk Lim

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The First Korean case of combined oxidative phosphorylation deficiency-17 diagnosed by clinical and molecular investigation by Young A Kim, Yoo-Mi Kim, Yun-Jin Lee, Chong Kun Cheon

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Successful rapid weight reduction and the use of liraglutide for morbid obesity in adolescent Prader-Willi syndrome by Yoo-Mi Kim, Yeoun Joo Lee, Soo Yeon Kim, Chong Kun Cheon, Han Hyuk Lim

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Case report of unexpected gastrointestinal involvement in type 1 Gaucher disease: comparison of eliglustat tartrate treatment and enzyme replacement therapy by Yoo-Mi Kim, Dong Hoon Shin, Su Bum Park, Chong Kun Cheon, Han-Wook Yoo

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Chronic intermittent form of isovaleric aciduria in a 2-year-old boy by Jin Min Cho, Beom Hee Lee, Gu-Hwan Kim, Yoo-Mi Kim, Jin-Ho Choi, Han-Wook Yoo

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Turner syndrome with primary hyperparathyroidism by Jungmee Park, Yoo-Mi Kim, Jin-Ho Choi, Beom Hee Lee, Jong Ho Yoon, Woon-Young Jeong, Han-Wook Yoo

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Lowe syndrome: a single center's experience in Korea by Hyun-Kyung Kim, Ja Hye Kim, Yoo-Mi Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo

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Comparison of effectiveness of growth hormone therapy according to disease-causing genes in children with Noonan syndrome by Kyo Jin Jo, Yoo Mi Kim, Ju Young Yoon, Yeoun Joo Lee, Young Mi Han, Han-Wook Yoo, Hyang-Sook Kim, Chong Kun Cheon

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A rare case of multiple pituitary adenomas in an adolescent Cushing disease presenting as a vertebral compression fracture by Ji-Yeon Song, Sue-Jean Mun, Soon-Ki Sung, Jae-Yeon Hwang, Seung-Kug Baik, Jee Yeon Kim, Chong-Kun Cheon, Su-Young Kim, Yoo-Mi Kim

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Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea by Yena Lee, Yunha Choi, Go Hun Seo, Gu-Hwan Kim, Changwon Keum, Yoo-Mi Kim, Hyo-Sang Do, Jeongmin Choi, In Hee Choi, Han-Wook Yoo, Beom Hee Lee

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Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase I/III Deficiencies Based on Clinical and Molecular Studies by Yoo-Mi Kim, Ja Hye Kim, Jin-Ho Choi, Gu-Hwan Kim, Jae-Min Kim, Minji Kang, In-Hee Choi, Chong Kun Cheon, Young Bae Sohn, Marco Maccarana, Han-Wook Yoo, Beom Hee Lee

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Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay by Go Hun Seo, Hane Lee, Jungsul Lee, Heonjong Han, You Kyung Cho, Minji Kim, Yunha Choi, Jeongmin Choi, In Hee Choi, Seonkyeong Rhie, Kyu Young Chae, Yoo-Mi Kim, Chong Kun Cheon, Su Jin Kim, Jieun Lee, Eungu Kang, Jung Hye Byeon, Hee Joon Yu, Young-Lim Shin, Arum Oh, Woo Jin Kim, Mi-Sun Yum, Beom Hee Lee, Baik-Lin Eun

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