1.Two Cases of Mercury Dermatitis Following Amalgam Dental Restorations.
Mi Hyung CHO ; Hwa Yung AHN ; Hong Il KOOK
Korean Journal of Dermatology 1985;23(5):650-653
Sensitivity to mercury appears to be not uncommon and perhaps the commonest contact with mercury in the general population is by amalgam dental restorations. Recently, we have experienced 2 cases of mercury dermatitis following amalgam dental restorations which were confirmed by the patch test. We report our cases with the patch test results and review the literatue on previous reports.
Dermatitis*
;
Patch Tests
2.Blood Level of Phenobarbital in Treatment of Seizure After Neonatal Asphyxia.
Ji Yean LEE ; Heng Mi KIM ; Doo Hong AHN
Journal of the Korean Pediatric Society 1989;32(9):1265-1272
No abstract available.
Asphyxia*
;
Phenobarbital*
;
Seizures*
3.A Study on Neonatal Hypoglycemia.
Oh Young KWON ; Chan Lak SON ; Haeng Mi KIM ; Kuhn Soo LEE ; Doo Hong AHN
Journal of the Korean Pediatric Society 1984;27(2):128-134
No abstract available.
Hypoglycemia*
4.A Clinical Study of Hereditary Spherocytosis.
Ki Ho KIM ; Kun Soo LEE ; Haeng Mi KIM ; Doo Hong AHN
Journal of the Korean Pediatric Society 1990;33(1):81-87
No abstract available.
5.Case of Chronic Pancreatitis Complicated Pancreatic Ascites and Pleural Effusion.
Gye Ja LEE ; Yong Aee CHUN ; Hey Sun LEE ; Yong Mi HONG ; Young Min AHN
Journal of the Korean Pediatric Society 1987;30(1):108-113
No abstract available.
Ascites*
;
Pancreatitis, Chronic*
;
Pleural Effusion*
6.A case of pseudohypoaldosteronism.
Yong Soon KWON ; Hyo Gyoung SHIN ; Mi Soo AHN ; Hong Bae KIM
Journal of the Korean Pediatric Society 1992;35(7):984-988
No abstract available.
Pseudohypoaldosteronism*
7.Serum Ferritin as an Indicator of Disease Activity in Adult Onset Still's Disease.
Gi Hyeon SEO ; Hong Joon AHN ; Hoon Suk CHA ; Jin Seok KIM ; Eun Mi KOH
The Journal of the Korean Rheumatism Association 1998;5(1):76-82
OBJECTIVE: Adult onset Still s disease is an acute systemic inflammatory disorder. There are no pathognomonic symptoms or specific laboratory abnormalities. In recent reports, serum ferritin concentration is increased in active disease phase and decreased after defervescence. Our purpose was to determine the clinical significance of serum ferritin as an indicator for disease activity. METHODS: Seven patients who were diagnosed as adult onset Still s disease at Samsung Medical Center between October 1994 and March 1997, were reviewed. In these patients we checked leukocyte count, ESR, CRP and serum ferritin concentrations at the time of diagnosis and during follow-up periods and recorded febrile events during follow-up periods. RESULTS: At the time of diagnosis and during febrile periods, the concentrations of ferritin were extremely high(927ng/ml to 96,650ng/ml normal 10-290.8 ng/ml). The values were unrelated to other manifestations of the disease or laboratory findings. The ferritin concentrations decreased rapidly after adequate treatment. Eleven febrile reattacks happened in 7 patients. Serum ferritin concentrations were increased in 8 febrile attacks, while leukocyte count, ESR, and CRP were increased in 5, 5, 6 febrile attacks respectively, There were 10 events of increased serum ferritin concentrations in 7 patients during follow-up periods and 8 events were related with fever. The increases of other laboratory tests were similar. CONCLUSIONS: In all patients, serum ferritin concentrations were increased at the time of diagnosis and closely related to fever. During follow-up periods, serum ferritin concentrations are helpful in monitoring disease activity and guiding decisions about treatment.
Adult*
;
Diagnosis
;
Ferritins*
;
Fever
;
Follow-Up Studies
;
Humans
;
Leukocyte Count
;
Still's Disease, Adult-Onset*
8.Diagnostic Significance of Free Fatty Acid, Lipase and beta-Glucuronidase in Breast Milk Jaunce.
Kyoung Ok LEE ; Soon Hak KWON ; Haeng Mi KIM ; Doo Hong AHN
Journal of the Korean Pediatric Society 1988;31(5):559-565
No abstract available.
Breast*
;
Glucuronidase*
;
Lipase*
;
Milk, Human*
9.Serum Iron Concentration of Maternal and Umbilical Cord Blood during Pregnancy.
Korean Journal of Community Nutrition 2005;10(6):860-868
Anemia diagnosed early in pregnancy is associated with increased risks of low birth weight and preterm delivery. The purposes of this study were to assess the maternal iron status during pregnancy and to evaluate the relationships between the iron indices of maternal-umbilical cord serum iron and ferritin levels and pregnancy outcomes. Dietary intakes of the pregnant women were estimated by 24 hour-recall (3 times). Serum iron and ferritin levels in maternal blood and umbilical cord were measured at 1st-, 2nd-, 3rd- trimester and delivery, respectively. The mean of maternal serum iron levels of the trimester and delivery were 124.27microgram/dl, 97.03microgram/dl, 94.32microgram/dl, and 145.53microgram/dl. Those maternal levels were significantly lower than that of umbilical cord blood (222.59microgram/dl). Serum ferritin levels of maternal trimester and delivery were 22.68microgram/l, 11.09microgram/l, 14.18microgram/l and 24.54microgram/l, which were significantly lower than those of umbilical cord blood (184.35microgram/l)(p<0.0001). This prevalence of anemia of total subjects was 30.3% by WHO criteria (Hb<11.0 g/dl, Hct<33%). Iron levels of 2nd-trimester was significantly higher in the normal group than in the anemia group. And ferritin levels of 3rd-trimester and delivery was significantly higher in the normal group than in the anemia group. Therefore, we suggest for successful pregnancy outcome and delivery differential iron supplementation programs will be carried out with individual pregnant women on the basis of pre-pregnancy nutrition.
Anemia
;
Female
;
Ferritins
;
Fetal Blood*
;
Humans
;
Infant, Low Birth Weight
;
Infant, Newborn
;
Iron*
;
Pregnancy Outcome
;
Pregnancy*
;
Pregnant Women
;
Prevalence
;
Umbilical Cord*
10.Clinical Studies of Urinary Tract Infection in Infant and Children.
Kee Sung YANG ; Mi Soo AHN ; Hong Bae KIM ; Ji Sub OH
Journal of the Korean Pediatric Society 1989;32(4):533-541
No abstract available.
Child*
;
Humans
;
Infant*
;
Urinary Tract Infections*
;
Urinary Tract*
Result Analysis
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