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Original Article
The Clinical Study on Acute Drug Intoxication in Children
W.H. Rhee, O.J. Koh, K.C. Sohn, K.S. Lee
Clin Exp Pediatr. 1975;18(6):453-456.   Published online June 30, 1975
A Clinical study on 45 cases with acute drug intoxication seen at N.M.C during the period of 14 years, from Jan. 1961 to Dec. 1974，was performed. The results following: 1)It occurr more frequently in male than female and more in under 1 year of age. 2) There was no significant difference in yearly distribution, these is no decreasing tendency. 3) The...
Symposium
Nutritional Requirement in Infants and Children
K.S. Lee
Clin Exp Pediatr. 1973;16(3):173-177.   Published online March 31, 1973
Pathogenesis of Edema and Application of Diuretics
K.S. Lee
Clin Exp Pediatr. 1972;15(4):277-282.   Published online April 30, 1972
Original Article
Clinical Observation of Congenital Pyloric Stenosis
C.K. Lee, T.I. Kim, T.K. Park, K.S. Lee
Clin Exp Pediatr. 1971;14(11):519-526.   Published online November 30, 1971
During last 12 years which was from 1958 to 1970, 11 cases of the congenital pyloric stenosis were admitted to department of pediatrics, N. M. C. and evaluated clinically. The results were obtained as follow： 1)The overall incidence of congenital pyloric stenosis was 0. 205% of all patients admitted to department of pediatrics, N. M. C. during this period, and the...
Case Report
A Case of Bochdalek’s Hernia
C.K. Lee, T.I. Kim, M.N. Lee, K.S. Lee
Clin Exp Pediatr. 1970;13(7):419-422.   Published online July 31, 1970
A case of surgically corrected congenital Bochdalek's hernia is reported. A 6 days old female baby was admitted with chief complaints of dyspnea and cyanosis. The diagnosis was confirmed by physical finding o£ the audible peristaltic sounds on the left chest and radiological characteristics. The hernia was succesfully corrected by transthoracic approach. The review of literature is made briefly.
Original Article
Statistical Anltysis of Death Cases(638 death cases were statistically analysed, especially comparisone between clinical and autopsy findings were made)
M.Z. Lee, T.I. Kim, K.S. Lee, C.H. Chi
Clin Exp Pediatr. 1970;13(4):191-200.   Published online April 30, 1970
The fetality rate by sex, age, season, of year and the group of diseases, the cause of gdeath by age and the underlying diseases, the rate of autopsy and misdiagnosis on 638 deaths in the total admitted 4,712 infantile and childhood patients admitted to the National Medical Center, Pediatric ward from 1958 to 1968, were observed in the view of...
Case Report
A Case of MeckeFs Diverticulum
T.I. Kim, S.K. Hong, M.N. Lee, K.S. Lee
Clin Exp Pediatr. 1970;13(1):45-48.   Published online January 31, 1970
A case of Meckel’s diverticulum complicated by hemorrhage was reported. Possible causes of intestinal bleeding were ruled out by laboratory examinations including whole hemogram, bone marrow examination, sigmoidoscopy, barium enema and upper G-I series. Consequently it was strongly suggested as Meckel’s diverticulum. Exploratory laparatomy was performed and the diverticulum was found. Wedge resection of the diverticulum was done with complete...
A Case Report of Hereditary Spherocytosis
K.S. Lee, K.O. Choi, J.U. Moon, C.S. Lee
Clin Exp Pediatr. 1968;11(11):583-586.   Published online November 30, 1968
A case of kreditary spherocytosis who was a 100 days old Korean male infant, was presented. Diagnosis was based on Splenomegaly, spherocytes in pheripheral blood and increased osmotic fragility. Any noticeable improvement was not observed by splenectomy and the patient expired 10 days after the splenectomy.
Vitamin D-Resistant Rickets
H.W. Kim, D.H. Bang, K.R. Kwak, K.S. Lee
Clin Exp Pediatr. 1968;11(6):321-328.   Published online June 30, 1968
Six cases of vitamin D resistant rickets are reported in Korean children, and comprehensive summary of clinical features and brief review of literatures are involved in this article. Two cases of them (15 and 7 years old boys respectively) were typical Fanconi syndrome with marked stunted growth, walking difficulty and valgus deformities in association with hypophosphatemia, renal glycosuria, marked aminoaciduria,...
A Case of Hereditary Spherocytosis
S.K. Hong, D.H. Bang, Y.H. Chung, K.S. Lee
Clin Exp Pediatr. 1968;11(1):23-26.   Published online January 31, 1968
A case of hereditary spherocytosis in a 13 years old Korean girl was presented. Splenectomy resulted in clinical cure. Review of literatures, especially of pathogenesis, was made briefly.
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