| 2017 | A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
| ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM |
| 2018 | A 6-year safety surveillance of 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) in South Korea.
| HUMAN VACCINES & IMMUNOTHERAPEUTICS |
| 2014 | A beneficial effect of rituximab on autoimmune thrombotic thrombocytopenic purpura: Just a B-cell depletion? | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY |
| 2017 | A boy with 46,X,+mar presenting gynecomastia and short stature
| ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM |
| 2022 | A Boy With Blau Syndrome Misdiagnosed as Refractory Kawasaki Disease
| Pediatric Infection & Vaccine |
| 2019 | A Case of Aplasia Cutis Congenita with Widespread Multifocal Skin Defects Without Extracutaneous Abnormalities | ACTA DERMATO-VENEREOLOGICA |
| 2006 | A Case of Cogential Fiber Type Disproportion With Multiple Anomalies
| Journal of the Korean Child Neurology Society |
| 2001 | A Case of del(13)(q22) with Multiple Major Congenital Anomalies, Imperforate Anus and Penoscrotal Transposition
| YONSEI MEDICAL JOURNAL |
| 2011 | A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome
| Journal of the Korean Child Neurology Society |
| 2014 | A case of eosinophilic fasciitis presenting as pitting edema of the lower extremities
| ALLERGY ASTHMA & IMMUNOLOGY RESEARCH |
| 2020 | A case of Galloway-Mowat syndrome with novel compound heterozygous variants in the WDR4 gene
| Journal of Genetic Medicine(대한의학유전학회지) |
| 2022 | A Case of Intellectual Disability without Epilepsy Associated with a Pathogenic Variant of STXBP1
| Annals of Child Neurology |
| 2002 | A Case of Intravenous Immunoglobulin-Resistant Kawasaki Disease Treated with Methotrexate
| YONSEI MEDICAL JOURNAL |
| 2011 | A Case of Mediastinal and Pulmonary Cryptococcosis in a 3-Year-Old Immunocompetent Girl
| Pediatric Allergy and Respiratory Disease (소아알레르기 호흡기학회지) |
| 2011 | A Case of Metachromatic Leukodystrophy Confirmed by Molecular Genetic Analysis
| Journal of the Korean Child Neurology Society |
| 2006 | A Case of Multiple Endocrine Neoplasia Type 2B early Diagnosis by RET Proto-oncogene Analysis and Proplactic TotalThyroidetomy
| Journal of Korean Society of Pediatric Endocrinology (대한소아내분비학회지) |
| 2005 | A case of multiple giant coronary aneurysms with large mural thrombus due to Kawasaki disease in a young infant
| Korean Journal of Pediatrics |
| 2022 | A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease with Acute Bilateral Total Blindness
| Annals of Child Neurology |
| 2010 | A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency | BRAIN & DEVELOPMENT |
| 2010 | A case of postoperative nasopharyngeal reflux associated with retropharyngeal lymphangioma in newborn infant
| Korean Journal of Pediatrics |
