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Original Article
A comparison Study on Soluble FcεR II/CD23 and IL-4 Activities nin the Serum of Children with Allergic and Non-allergic Diseases
Ha-Baik Lee, Han Young Lee, Hahng Lee
Clin Exp Pediatr. 1992;35(3):296-305.   Published online March 15, 1992
Allergy classically rfes to hypersensitivity reaction induced by chemical mediators released from mast cells and basophils activaed by binding allergens contained in house dust, animal dander, pollen, fungus, food and others to IgE (reaginic antibody) bound on these cells. The significance of low affinity Fc receptor for IgE ( FcεR II, CD23, FcεR II/CD23) on B and T lymphocyts, macrohage ,...
Clinical Studies of Brain Tumors in Children.
In Hee Park, Han Young Lee, Jeh Hoon Shin, In Joon Seol, Woo Gill Lee, Hang Lee
Clin Exp Pediatr. 1985;28(11):1082-1088.   Published online November 30, 1985
During a period of 116/12 years, from July, 1974 to December, 1984, 44 cases under 15 years of age with brain tumors were observed at department of pediatrics and neurosurgery at Hanyang University Hospital. The results were as follows: 1)The peak incidence of age was observed in the children from 5 to 10 years (38.6%). The sex ratio of male to...
So-called 'Septal Aneurysm' in membranous Ventricular Septal defect.
Han Young Lee, In Hee Park, Ha Baik Lee, Heung Jae Lee
Clin Exp Pediatr. 1985;28(9):869-879.   Published online September 30, 1985
During the period of 4 years from October, 1980 to September, 1984, 28 cases with septal aneurysm in membranous ventricular septal defect were observed and evaluated at Hanyaeng University Hospital, and those were confirmed by LV angiogram and/or 2D-echocardiogram. We also correlated the findings of aneurysm of the membranous septum with clinical, electrocardiographic and hemodynamic data for use in noninvasive...
Case Report
A Case of Achondroplasia.
Han Young Lee, Seon Ock Khang, Woo Gill Lee
Clin Exp Pediatr. 1984;27(12):1234-1238.   Published online December 31, 1984
Achondroplasia, the commonest type of dwarfism, is an autosomal-dominant skeletal dysplasia in which the primary defect is endochondral bone formation. Characteristic clinical findings are large head size, rhizomelic shortening of the limbs, frontal bossing & flat nasal bridge with X-ray findings of brachycephaly, thickness of long bone, squared iliac bone and decreased interpediculate distance of spine at distal lumbar level compared with proximal. Authors experienced a...
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