교원정보

학술지 논문

• (2022)  Hypertriglyceridemia with acute pancreatitis in a 14-year-old girl with diabetic ketoacidosis.  Annals of Pediatric Endocrinology & Metabolism.  27,  1
• (2021)  Impact of growth hormone treatment on scoliosis development and progression: analysis of 1128 patients with idiopathic short stature.  JOURNAL OF PEDIATRIC ENDOCRINOLOGY METABOLISM.  34,  2
• (2021)  Tailored management of life-threatening complications related to severe obesity in a young adult with Prader-Willi syndrom.  Annals of Pediatric Endocrinology & Metabolism.  10,  10
• (2021)  Wilson disease diagnosed incidentally by targeted gene panel sequencing in a Korean boy with severe obesity.  Annals of Pediatric Endocrinology & Metabolism.  10,  10
• (2021)  Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome.  FRONTIERS IN ENDOCRINOLOGY.  12,  1
• (2021)  Efficacy and safety of the recombinant human growth hormone in short children born small for gestational age A randomized, multicentre, comparative phase III trial.  MEDICINE.  100,  30
• (2021)  Long-Term Antithyroid Drug Treatment of Graves' Disease in Children and Adolescents: A 20-Year Single-Center Experience.  FRONTIERS IN ENDOCRINOLOGY.  12,  1
• (2021)  Clinical characteristics, treatment outcomes, and occurrence of diabetes mellitus after pancreatic resection of solid pseudopapillary tumor in children and adolescents: A single institution experience with 51 cases.  PANCREATOLOGY.  21,  3
• (2021)  Clinical Presentation and Treatment Outcomes of Children and Adolescents With Pheochromocytoma and Paraganglioma in a Single Center in Korea.  FRONTIERS IN ENDOCRINOLOGY.  11,  1
• (2020)  The First Korean Case of Baraitser-Winter Cerebro-Fronto-Facial Syndrome with a Novel Mutation in ACTB Diagnosed Via Targeted Gene Panel Sequencing and Literature Review.  ANNALS OF CLINICAL AND LABORATORY SCIENCE.  50,  6
• (2020)  The First Korean Family with Aarskog-Scott Syndrome Harboring a Novel Mutation in FGD1 Diagnosed via Targeted Gene Panel Sequencing.  ANNALS OF CLINICAL AND LABORATORY SCIENCE.  50,  5
• (2020)  Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center.  FRONTIERS IN ENDOCRINOLOGY.  11,  1
• (2020)  Primary headache in childhood associated with psychiatric disturbances: an update.  EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES.  24,  12
• (2020)  Nonclassic congenital lipoid adrenal hyperplasia diagnosed at 17 months in a Korean boy with normal male genitalia: emphasis on pigmentation as a diagnostic clue.  Annals of Pediatirc Endocrinology & Metabolism.  25,  1
• (2020)  A boy with Coffin-Siris syndrome with a novel frameshift mutation in ARID1B.  NEUROENDOCRINOLOGY LETTERS.  41,  6
• (2019)  Auditory Characteristics in Patients With Mucopolysaccharidosis.  OTOLOGY & NEUROTOLOGY.  40,  10
• (2019)  Impact of BMI on peak growth hormone responses to provocative tests and therapeutic outcome in children with growth hormone deficiency.  SCIENTIFIC REPORTS.  9,  1
• (2019)  Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial.  ORPHANET JOURNAL OF RARE DISEASES.  14,  1
• (2019)  Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrum.  ANNALS OF HUMAN GENETICS.  83,  3
• (2019)  Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family.  JOURNAL OF GLAUCOMA.  28,  4