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Case Report
Three Cases of Juveile Diabetes Mellitus . Occurring in Siblings
Jae Jung Choi, Suk Hyeon Yun
Clin Exp Pediatr. 1974;17(2):154-160.   Published online February 28, 1974
This paper presents 3 cases of Juvenile diabetes mellitus occurreed in 3 out of 5 siblings, who were 11,10 and 9 year old respectively. The diagnosis was confirmed by oral glucose tolerance tests in Case I and II. Either familial tendency of diabetes melltus or other genetic disorder in their family were not informed. Brief reviews of literatures are added.
Original Article
Serum Calcium and Phosphorus in Premaiure and Full-Term Infants
Jae Jung Choi
Clin Exp Pediatr. 1974;17(2):103-110.   Published online February 28, 1974
Neonatal hypocalcemia occurs in full-term infants, and more frequently; in premature infants. Various etiologic factors for hypocalcemia of new-born infants have been proposed in the litera- tures: parathyroid1 insufficiency or functionally imature parathyroid, serum phosphorus levels,, fasting and various diets, rate* of growth and vitamin- D deficiency. There was large literature on the sa-called normal serum calcium level in newborn infant, but less was known...
The Effect of a High Calorie Diet on the Weight of Premature Babies
Jae Jung Choi, Suk Kyu Kim, Young Won Kim
Clin Exp Pediatr. 1973;16(3):219-225.   Published online March 31, 1973
Of a total of 699 premature babies admitted to the pediatric dept, of I.S.W.H. during 13 months from 1 July 1971 to 31 July 1972, 306 babies were suitable for study. Of these 151 were given 5% glucose in water and 155 were given glucose in water as initial feeding and the following results were obtained using the birth weight...
Case Report
A Case of Progressive Muscular Dystrophy(Facioscapulohumeral type of Landouzy-Dejerine)
Doo Hyun Lee, Jae Jung Choi, Kyung Ja Yoon
Clin Exp Pediatr. 1973;16(1):66-71.   Published online January 31, 1973
A case of progressive muscular dystrophy(Facioscapulohumeral type df Landouzy-Dejerine) occurring in a 15-year-old girl was reported, which has marked familial tendency with autosomal dominant pattern, typical clinical pictures involving muscles of face, upper arm and shoulder girdle and typical histologic findings showing scattered atrophic muscle fibers, and hyalinization and fragmentation of muscle fibers in muscle biopsy. The creatinine and creatinine...
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