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Volume 16(7); Jul 1973
Immunolo Mie Response
Y.S. Ki
J Korean Pediatr Soc. 1973;16(7):505-511.   Published online July 31, 1973
Thymus and Immunity
K.Y. Chang
J Korean Pediatr Soc. 1973;16(7):512-519.   Published online July 31, 1973
Human Plasma Immunoglobulins
B.S. Shim
J Korean Pediatr Soc. 1973;16(7):520-522.   Published online July 31, 1973
Maturation of Immunologic Function
Jongwoo Shin
J Korean Pediatr Soc. 1973;16(7):523-525.   Published online July 31, 1973
Immune Deficiency Disorders
Myunghee Shin
J Korean Pediatr Soc. 1973;16(7):526-530.   Published online July 31, 1973
Hypersensitivity Diseases
C.J. Kim
J Korean Pediatr Soc. 1973;16(7):531-534.   Published online July 31, 1973
Autoimmune Diseases
W.C. Kim
J Korean Pediatr Soc. 1973;16(7):535-538.   Published online July 31, 1973
Diagnostic Tests in Immune Deficiency Diseases
S.L. Kim
J Korean Pediatr Soc. 1973;16(7):539-542.   Published online July 31, 1973
Original Article
Experimental Studies of Acute Liver Damage in Young White Rats
Chong Ku Yun
J Korean Pediatr Soc. 1973;16(7):543-564.   Published online July 31, 1973
This study was attempted to analysis whether there are any differences or not in the susceptibility to acute liver damage due to chemical hepato-toxic agents between young white rat and mature one. The experiment was carried out in four divided groups as follows; control group, CC14 group, chloroform group, and ethionine group. Each group was subdivided again into weight of...
Case Reports
Muco-Cutaneous Lymphnode Syndrome(Five Cases Report)
Chung Sook Park, Choon Ji Suh, Sung Hoon Cho, Du Bong Lee
J Korean Pediatr Soc. 1973;16(7):565-571.   Published online July 31, 1973
So-called Muco-Cutaneous Lymphnode Syndrome (MCLS) was reported first in 1967 by Tomisaku Kawasaki Department of Pediatrics, Japanese .Red Cross Central Hospital, Tokyo, Japan and then over 1,857 cases of this syndrome has been reported in Japan recently until 1971. This syndrome was characterized by the continued high fever durated over 10 days. The swelling of cervical lymphnodes simulating Mumps, generalized...
A Case Report of Hereditary Spherocytosis
Yong Kuk Kim, Chung Sook Park, Chung Kyu Kim, Man Kyu Yang
J Korean Pediatr Soc. 1973;16(7):572-576.   Published online July 31, 1973
A case of hereditary spherocytosis who was a 14 years old Korean female, was presented. The diagnosis was confirmed by physical findings, spherocytes in pheripheral blood, bone marrow, and increased red cell osmotic fragility. None of her four members of family has similar disease. Pertinent literature were reviewed briefly.
Abstract from Foreign Literature
J Korean Pediatr Soc. 1973;16(7):577-578.   Published online July 31, 1973
Literature Index of Foreign Journals
J Korean Pediatr Soc. 1973;16(7):579-583.   Published online July 31, 1973
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