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이상락,장성진,권태찬 啓明大學校 醫科大學 1992 계명의대학술지 Vol.11 No.3
The electrocardiographic and hemodynamic analysis were made on 50 patients with patent ductus arteriosus which were diagnosed by echocardiography and cardiac catheterization at Dong San Hospital Keimyung University during the period of 4 years from January 1987 to December 1990. A total of 50 patients, 17 were male and 33 were female. Their ages ranged from 6 months to 15 years. The QRS axis were as follows in orders: normal axis(72.0%), right axis deviation(22.0%) and left axis deviation(6.0%). The large diphasic QRS complex in precordial lead V₁ was encounted in 54.0% of the cases. When the R/S ratio in V₁ was more than upper limit of normal, the right ventricular systolic pressure was significantly higher than that of the R/S ratio less than lower limit of normal(P<0.001). When the RIS ratio in V?? was less than lower limit of normal, the right ventricular systolic pressure was significantly higher than that of the R/S ratio more than upper limit of normal(P<0.001). When a normal electrocardiographic pattern was present, the right ventricular systolic pressure was normal. When left ventricular hypertrophy pattern was present, the right ventricular systolic pressure was moderately increased but biventricular and right ventricular hypertrophy was present, the right ventricular systolic pressure was markedly increased. There was statistically significant relationship between electrocardiographic pattern and right ventricular systolic pressure (P <0.001). There was a good correlation between the amplitude of S wave in lead V?? and right ventricular systolic pressure(r=0.9).
권영대,권태찬 啓明大學校 醫科大學 1982 계명의대학술지 Vol.1 No.1
We have experienced two cases of paraquat poisoning which had taken the drug for suicide. A 14-year-old girl and 9-year-old boy expired form respiratory failure in 24 and 15 days after ingestion of paraquat respectively.
권태찬,김준식,이상락,박근수,강진무,김명성,전효진 啓明大學校 醫科大學 1992 계명의대학술지 Vol.11 No.4
Authors experienced a case of Patau syndrome in a 1 day old male, born to the mother aged 34 years. He was born with multiple congenital anomalies such as microcephaly, malformed low-set ears, cleft lip and palate, cryptorchidism, anomalous scrotum, micropenis, clenched hand and Rockerbottom feet. Tetralogy of Fallot and atrioventricular canal defect were detected by echocardiography, and chromosomal analysis showed 47 chromosomes with 13 trisomy. He died at 9th day of life. A brief review of the literature was made.
권태찬,김은아,박근수,이성문,이상락 啓明大學校 醫科大學 1995 계명의대학술지 Vol.14 No.3
Subphrenic abscess was a very rare condition in early infancy and there were no reports of this in Korea yet. We experienced a case of subphrenic abscess in a 2-month-old male infant who had the symptoms of diarrhea and abdominal distension, and diagnosed with abdominal ultrasonogram and computed tomography, and treated successfully with percutaneous drainage and antibiotics.
Incidence of Intestinal Amebas in Persistent Diarrheic Patients
Kwon,Tae Chan,Choi,Dong Wik 啓明大學校 醫科大學 1983 계명의대학술지 Vol.2 No.1
1979年 3月부터 1981年 2月까지 慢性泄瀉와 痢疾樣症狀으로 慶北醫大 附屬病院에 來院하여 奇生 蟲學校室에서 原 檢査를 받은 被檢者에서의 名種 아메바의 檢出狀을 究明함과 함께 李(1979)의 成績과 比較하였다. 아메바의 同定에는 iron-hematoxylin 染色法을 使用하였다. 被檢者 2,083名 중 痢疾아메바 胞囊의 檢出率은 54.6%, 大腸아메바의 그 率은 8.4%였으며 矮少아메바와 沃度아메바는 各各 1.2% 및 0.8%로 드물게 檢出되었다. 痢疾아메바胞囊의 性別檢出卒에 있어서는 男女問에 有意的 差를 認定할 수 없었으며, 年齡別로는 20~29歲群에서 最大値를, 0~9歲群에서 最少値를, 月別로는 8月에 最大値, 10月에 最少値를 나타내었고, 總檢出率은 1979年에 比해 1981年에 높았다.
김준식,권태찬,강진무,전석길,서수지,이광숙,유영선 啓明大學校 醫科大學 1991 계명의대학술지 Vol.10 No.1
Pulmonary atresia with intact ventricular septum is uncommon congenital cardiac anomaly constituting less than 1% of congenital heart disease. Authors experienced a case of pulmonary atresia with intact ventircular septum in a 95 day-old male. Diagnostic confirmation was made by 2-D echocardiography, cardiac catheterization and angiography. Right ventricular outflow reconstruction with Xenomedica, tricupid valve commissurotomy, closure of patent foramen ovale, and concomitant pumonary valvectomy were performed surgically.
Supravalvar Aortic Stenosis 1례 : Williams Syndrome
김성호,권태찬,강진무 啓明大學校 醫科大學 1987 계명의대학술지 Vol.6 No.2
Williams syndrome is an uncommon congenital anomaly which is composed of supravalvar aortic stenosis, peculiar face (elfin facies) and mental retardation. Authors experienced a case of Williams syndrome in a 7 year old girl who had a peculiar face and mental retardation. Diagnosis of supravalvar aortic stenosis was established by catheterization and angiocardiography and aided by EKG and 2-D echocardiography. Aortic stenosis was corrected by surgery and discharged in a good condition. A brief review of the literature was made.