1.Clinical observation on juvenile theumatoid arthritis.
Journal of the Korean Pediatric Society 1991;34(8):1123-1131
No abstract available.
Arthritis*
;
Arthritis, Juvenile
2.A case of distal type of renal tubular acidosis in a neonate.
Sung Sub SHIM ; Young Joon KIM ; Jae Hong PARK ; Soo Yung KIM ; Chan Yung KIM
Journal of the Korean Pediatric Society 1992;35(7):1014-1018
No abstract available.
Acidosis, Renal Tubular*
;
Humans
;
Infant, Newborn*
3.Morphometric Study on the Development of the Human Fetal Heart after Mid-term.
Ho Dirk KIM ; Chul Woo KIM ; Bong Jin RAH ; Hae Sung LEE ; Tae Sub SHIM
Korean Journal of Physical Anthropology 1990;3(1):1-12
A total of 23 human fetal hearts from 18 to 40 weeks of gestation were provided for histologic and morphometric studies. The fetuses were the products of spontaneous or artificial abortions and were found to have no congential anomalies or associated lesions at autopsy. Maxima thickness of the left anterior, left lateral, left posterior, right anterior, right lateral, right posterior ventricular wall, and of the interventricular septal wall were measured and the left / right wall thickness ratio was calculated. The cross-sectional area of each ventricle parallel to the base of the heart at about 3-5mm below from the origin of the aorta was measured under drawing attachment-equipped light microscope with the application of point counting or cut-and-weigh method. Data were analyzed by the Anderson-ell ABSTAT dBASE ll statistical package program. The ventricular wall consisted of endocardium, myocardium and epicardium. The myocardium showed epithelial character by stratification of barrel-shaped myocardial cells, but the epithelial character progressively changed to as in adult myocardial tissue from the myocardial area close to the epicardium with increasing fetal age. However, any significant histologic difference between the left and the right ventricular wall at the same fetal age was not found. The growth pattern of both ventricular wall, the interventricular septal wall, and of the cross sectional area were linear (p<0.01). However, there was no significant difference in the wall thickness between the left and right ventricle at the same fetal age, and the left / right thickness ratio was nearly constant with increasing fetal age. The cross sectional area was greater in the right than in the left ventricle in the fetuses after 18 weeks of gestation (p<0.01), and there was no significant difference in the morphometric values between point counting and cut-and-weigh method (p>0.1).
Adult
;
Aorta
;
Autopsy
;
Endocardium
;
Fetal Heart*
;
Fetus
;
Gestational Age
;
Heart
;
Heart Ventricles
;
Humans*
;
Methods
;
Myocardium
;
Pericardium
;
Pregnancy
4.In Vitro Release of L-dopa and Dopamine by Genetically Modified Fibroblasts of the Rat.
Journal of Korean Neurosurgical Society 1993;22(4):529-536
A construct DNA containing the cDNA for rat tyrosine hydroxylase(TH) and another construct DNA containing the cDNA for bovine L-dopa decarboxylase(DDC) were made and those genes were transferred by calcium phosphate transfection method into the immortalized rat fibroblasts. A both TH- & DDC-positive clone was identified by immunocytochemical staining. These cells produced L-dopa and dopamine and released them into the cell culture medium in vitro, which was confirmed by high performance liquid chromatography. These results have general implications for the application of gene therapy and specific implications for Parkinson disease.
Animals
;
Calcium
;
Cell Culture Techniques
;
Chromatography, Liquid
;
Clone Cells
;
DNA
;
DNA, Complementary
;
Dopamine*
;
Fibroblasts*
;
Genetic Therapy
;
Levodopa*
;
Parkinson Disease
;
Rats*
;
Transfection
;
Tyrosine
;
Tyrosine 3-Monooxygenase
5.In Vitro Release of L-dopa and Dopamine by Genetically Modified Fibroblasts of the Rat.
Journal of Korean Neurosurgical Society 1993;22(4):529-536
A construct DNA containing the cDNA for rat tyrosine hydroxylase(TH) and another construct DNA containing the cDNA for bovine L-dopa decarboxylase(DDC) were made and those genes were transferred by calcium phosphate transfection method into the immortalized rat fibroblasts. A both TH- & DDC-positive clone was identified by immunocytochemical staining. These cells produced L-dopa and dopamine and released them into the cell culture medium in vitro, which was confirmed by high performance liquid chromatography. These results have general implications for the application of gene therapy and specific implications for Parkinson disease.
Animals
;
Calcium
;
Cell Culture Techniques
;
Chromatography, Liquid
;
Clone Cells
;
DNA
;
DNA, Complementary
;
Dopamine*
;
Fibroblasts*
;
Genetic Therapy
;
Levodopa*
;
Parkinson Disease
;
Rats*
;
Transfection
;
Tyrosine
;
Tyrosine 3-Monooxygenase
6.Statistical Observation for Admitted Patients during the Years of 1974 to 1977 at Ped. Dept. of Han-Il Hospital.
Yong Sub KANG ; Sung Won PARK ; Kwang SHIM ; Yeun Ki KIM ; Yong Il LEE
Journal of the Korean Pediatric Society 1979;22(4):262-291
Statistical analysis according to W.H.O. classification for the patients admitted the Ped. Dept. of Han-Il Hospital was carried out during 4 years from Jan. 1974 to Dec. 1977. The following results were observed. 1. Total No. of patient during 4 years period were 1955, of which 1199 were male(61.33%, 756 were female(38.67%) and male to femal ratio was 1.57:1. 2. There was no significant variation. 3. According to age, preschool aged group as the most frequent group consistin of 488 cases(24.49%), school aged group and adolescent in the order of frequency. 4. On monthly distribution, there was no significant variation 5. Most frequent diseases in pediatric age group were respiratory tract one, 851 cases(39.29%) : infectious and parasitic ones, 553(25.53%) and neonatal disease, 204 cases(9.42%) in the order of frequency. 6. Among respiratory tract disease, pneumonia was the most frequent one, 587 cases(27.10%). 7. Among infectious and parasitic disease group, gastrointestinal infectious one was the most frequent, 224 cases(10.34%) : other viral disease and tuberculosis in the order of frequency. 8. Among neonatal diseases, prematurity was the most frequent one, 82 cases(3.79%).
Adolescent
;
Classification
;
Humans
;
Male
;
Parasitic Diseases
;
Pneumonia
;
Respiratory System
;
Respiratory Tract Diseases
;
Tuberculosis
;
Virus Diseases
7.Three Cases of Coronary Artery Fistula from Right Coronay to Left Ventricle.
Sung Hwa BAE ; Bong Jun KIM ; Jong Seon PARK ; Dong Goo SHIN ; Young Jo KIM ; Bong Sub SHIM
Korean Circulation Journal 1998;28(7):1216-1216
The coronary artery fistula from right coronary artery to left ventricle is a rare disease among coronary artery anomaly. We experienced three cases of rare coronary fistula and report with literature review. Although symptoms of coronary artery fistula are associated with arteriovenous shunt and coronary steal phenomenon, many cases are asymptomatic. In this report, all patients had no symptom. but incidental murmur was noted (two are continuous, one is diastolic rumbling). The diagnosis was made by transthoracic or transesophageal echocardiogram and selective coronary angiography. Because patients were relatively young and the diameter of dilated coronary artery were huge, we perfomed operation on three patients.
Coronary Angiography
;
Coronary Vessels*
;
Diagnosis
;
Fistula*
;
Heart Ventricles*
;
Humans
;
Rare Diseases
8.Rifabutin susceptibility and rpoB gene mutations in multi-drug resistant mycobacterium tuberculosis.
Tae Sun SHIM ; Jin Sub KIM ; Mi Sun PARK ; Chae Man LIM ; Sang Do LEE ; Youn Suk KOH ; Woo Sung KIM ; Dong Soon KIM ; Won Dong KIM
Tuberculosis and Respiratory Diseases 2000;48(6):853-869
BACKGROUND: Following several decades of decline, the incidence of tuberculosis has recently begun to increase in many countries and the control of this disease has been impeded by the emergence of multi-drug resistant tuberculosis (MDR-TB). The development of rapid diagnostic methods and effective new drugs are needed to control MDR-TB. One of the new drugs for MDR-TB is rifabutin (RBU) which has been known to be effective in some patients with MDR-TB. A few reports showed that some types of mutaitions of the rpoB gene, which were known to be present in 96-98% of rifampicin-resistant M. tuberculosis, were associated with the rifampicin-resistant but RBU-susceptible phenotype. This study was performed to investigate the correlation between RBU susceptibility and the patterns of rpoB gene mutations in Korean MDR-TB. METHODS: Sixty-five clinical isolates of multi-drug resistant Mycobacterium tuberculosis, gathered from patients two visited the Asan Medical Center from July 1997 to June 1999, were investigated. Clinical responses to rifabutin-containing regimen were evaluated. An RBU susceptibility test and sequencing analysis of rpoB gene were performed, and the result were analyzed to confirm which mutations correlated with RBU-susceptible MDR-TB. RESULTS: Fifty-three of 56 (95%) clinical isolates of MDR-TB had 60 mutations of the rpoB gene. The most frequent mutations were found at codon 531 (43%), and two mutations were combined in seven clinical isolates. Five of 53 (10%) clinical isolates showed the RBU-susceptible phenotype, and in them the characteristic patterns of point mutations were found at codon 509, 516, and 526. CONCLUSION: The frequency and pattern of mutations of the rpoB gene of Korean MDR-Tb isolates were similar to those in western countries, where the prevalence of tuberculosis is low, but some show RBU-susceptible phenotypes. RBU-susceptible MDR-TB isolates showed the characteristic pattern of mutations of the rpoB gene which could be used to rapidly diagnose RBU susceptibility.
Chungcheongnam-do
;
Codon
;
Humans
;
Incidence
;
Mycobacterium tuberculosis*
;
Mycobacterium*
;
Phenotype
;
Point Mutation
;
Prevalence
;
Rifabutin*
;
Tuberculosis
;
Tuberculosis, Multidrug-Resistant
9.Analysis of Asymptomatic Proteinuria in School Children.
Chong Guk LEE ; Tae Sub SHIM ; Dong Hwan LEE ; Yong Soo YUN ; Chang Jun KO ; Sa Jun CHUNG ; Hyun Soon LEE ; Sung Jae SUH ; Pyung Nam KIM
Journal of the Korean Pediatric Society 1989;32(9):1187-1194
No abstract available.
Child*
;
Humans
;
Proteinuria*
10.Neonatal Tetany Caused by Hyperparathyroidism Undetected During Pregnancy.
Wan Sub SHIM ; Hee Baek PARK ; Bong Soo CHA ; Sung Kil LIM ; Hyun Chul LEE ; Kap Bum HUH
Journal of Korean Society of Endocrinology 2002;17(2):257-262
Primary hyperparathyroidism is rarely encountered during pregnancy but its prompt diagnosis and treatment if encountered during pregnancy is important because it can carry considerable morbidity not only for the mother but also for the fetus. It tends to remain undiagnosed because 50~80% of the patients are asymptomatic. Even if they do demonstrate symptoms, those are often nonspecific. The other reason for non-diagnosis is masking of hypercalcemia due to the change of calcium homeostasis during pregnancy. Neonatal tetany can be a clue for the presence and diagnosis maternal hyperparathyroidism. The asymptomatic patient who is diagnosed postpartum when her newborn is symptomatic should undergo elective parathyroidectomy to avoid future complication. We experienced a woman with undiagnosed primary hyperparathyroidism during pregnancy whose two children suffered neonatal tetany. We report this case along with a review of literature on primary hyperparathyroidism in pregnancy and calcium homeostasis during pregnancy.
Calcium
;
Child
;
Diagnosis
;
Female
;
Fetus
;
Homeostasis
;
Humans
;
Hypercalcemia
;
Hyperparathyroidism*
;
Hyperparathyroidism, Primary
;
Infant, Newborn
;
Masks
;
Mothers
;
Parathyroidectomy
;
Postpartum Period
;
Pregnancy*
;
Tetany*