A Korean boy with a mutation who presented with overgrowth, intellectual disability, and autism by Chiwoo Kim, Eu-seon Noh, Sung Yoon Cho

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Mixed diabetic ketoacidosis and hyperglycemic hyperosmolarity in a girl with nephronophthisis 4 presenting with rhabdomyolysis and pancreatitis by Eu-Seon Noh, Chiwoo Kim, Sung Yoon Cho

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α-Klotho levels in girls with central precocious puberty: potential as a diagnostic and monitoring marker by Jun-Hong Park, Eu-Seon Noh, Il Tae Hwang

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Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation by Jiyeon Kim, Eu Seon Noh, Min-Sun Kim, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho

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Endocrine and Metabolic Illnesses in Young Adults with Prader–Willi Syndrome by Eu-Seon Noh, Min-Sun Kim, Chiwoo Kim, Kyeongman Jeon, Seonwoo Kim, Sung Yoon Cho, Dong-Kyu Jin

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Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III by Min-Sun Kim, Aram Yang, Eu-seon Noh, Chiwoo Kim, Ga Young Bae, Han Hyuk Lim, Hyung-Doo Park, Sung Yoon Cho, Dong-Kyu Jin

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First female Korean child with Coffin-Lowry syndrome: a novel variant in diagnosed by exome sequencing and a literature review by Ari Song, Minji Im, Min-Sun Kim, Eu Seon Noh, Chiwoo Kim, Jahyun Jang, Sae-Mi Lee, Chang-Seok Ki, Sung Yoon Cho, Dong-Kyu Jin

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Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome by Sung Yoon Cho, Danbee Kang, Minji Im, Aram Yang, Min-Sun Kim, Jiyeon Kim, Eu-Seon Noh, Eun Kyung Kwon, Eujin Choi, Sunju Han, Young Ah Park, Min Jung Kwak, Youngha Kim, Juhee Cho, Dong-Kyu Jin

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