Pevalence of hyperuricemia and its association with metabolic syndrome and cardiometabolic risk factors in Korean children and adolescents: based on the 2016-2017 Korea National Health and Nutrition Examination Survey. Korean J Pediatr. 2019;62:317-23.
The Effect of Delayed Elevation of Thyrotropin on Feeding Intolerance in Very Low Birth Weight Infants. Neonatal Medicine. 2019;26:102-10.
Blood lead concentrations and attention deficit hyperactivity disorder in Korean children: a hospital-based case control study. BMC Pediatr. 2016;16:156.
Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam. Ann Pediatr Endocrinol Metab. 2015;20:206-12.
Psychological Characteristics and Attention of Children with Short Stature : Multicenter, Case-control Study. J Korean Soc Biol Ther Psychiatry. 2015;21:174-80.
Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency. J Hum Genet. 2015;60:501-7
OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patients. Pediatr Neurol. 2014;51:354-9
Dietary patterns in children with attention deficit/hyperactivity disorder (ADHD). Nutrients. 2014;6:1539-53.
Severe dapsone hypersensitivity syndrome in a child. Korean J Pediatr. 2013;56:260-4.
The Study in Vitamin D Concentration in the Blood for Infants with High Level of Alkaline Phosphatase. Kosin Med J. 2012;27:17-24.
Assessment of Iron Parameters in Children with Acute Infectious Disease. Clin Pediatr Hematol Oncol. 2012;19:72-7.
High allele frequency of the p.Q258X mutation and identification of a novel mis-splicing mutation in the STAR gene in Korean patients with congenital lipoid adrenal hyperplasia. Eur J Endocrinol. 2011;165:771-8.
Clinical characterization and identification of two novel mutations of the GNAS gene in patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism. Clin Endocrinol (Oxf). 2011;75:207-13.
A 9-month-old phosphaturic mesenchymal tumor mimicking the intractable rickets. J Pediatr Orthop B. 2010;19:127-32.
Effects of Family Environment and Parenting Behavior on Glycemic Control and Depressive Symptoms in Children with Type 1 Diabetes. J Korean Soc Pediatr Endocrinol. 2009;14:100-109.
Growth Assessment of Children and Adolescents Complaining of Short Stature. Kosin Med J. 2008;23:42-8.
Long-term Follow-up Outcome in Children and Adolescents with Hashimoto's Thyroiditis. J Korean Soc Pediatr Endocrinol. 2008;13:163-72.
A Case of Achodroplasia Confirmed by Mutation Analysis of FGFR3 Gene. Kosin Med J. 2008;23:90-4.
A Case of Prader-Willi Syndrome with Hypotonia and Cryptorchidism Diagnosed at Neonate. Kosin Med J. 2007;22:186-90.
A case of a Korean newborn with IMAGe association presenting with hyperpigmented skin at birth. Eur J Pediatr. 2007;166:879-80.
AGL gene mutation and clinical features in Korean patients with glycogen storage disease type III. Journal of the Korean Society of Inherited Metabolic Disease 2006;6:15-23.
Clinical Characteristics of Type 2 Diabetes in Children and Adolescents. J Korean Soc Pediatr Endocrinol. 2006;11:64-9.
Clinical Course and Outcome Thyroid Carcinoma in Childhood. J Korean Soc Pediatr Endocrinol. 2006;11:57-63.
A case of Propionic Acidemia with Gait Disturbance. Journal of the Korean Society of Inherited Metabolic Disease 2006;6:6-14.
Paternity Test by Analysis of HLA Antigens. Kosin Med J. 2006;21:133-8.
A Case of Rothmund-Thomson Syndrome with Pure Red Cell Aplasia, Autoimmune Hemolytic Anemia and Chronic Respiratory Infection. Korean J Pediatr. 2004;47:1351-5.
저서
희귀난치성질환의 이해 IX (공저) 희귀난치성질환 총서 35-51 희귀난치성질환의 이해 XI (공저) 희귀난치성질환 총서 55-65 알면 알수록 건강해지는 제1형 당뇨병 안내서 (공저) 부산당뇨병캠프