1.Choledochal Cyst.
Korean Journal of Medicine 2004;66(1):100-101
No abstract available.
Choledochal Cyst*
2.A study on the moral development in medical students (II).
Man Hong LEE ; Joon Ki KIM ; Eun Yong CHOE
Journal of Korean Neuropsychiatric Association 1991;30(2):402-413
No abstract available.
Humans
;
Moral Development*
;
Students, Medical*
3.Adenomyomatosis of gall bladder.
IL Bong KIM ; Ki Man LEE ; Mun Gyu PARK
Korean Journal of Medicine 2002;63(4):436-437
No abstract available.
Urinary Bladder*
4.Snuffbox arteriovenous fistula.
Yoon Ki MIN ; Wook KIM ; Jong Man WON
Journal of the Korean Surgical Society 1992;43(1):118-122
No abstract available.
Arteriovenous Fistula*
5.Rheumatoid cervical involvement.
In KIM ; Jung Man KIM ; Han CHANG ; Youn Soo KIM ; Ki Won KIM
The Journal of the Korean Orthopaedic Association 1993;28(2):594-606
No abstract available.
6.Clinical analysis of imperforate anus.
Si Man LEE ; Gie Hwa YOON ; Sang Ki MIN ; Sung Hwan KIM ; Chan Yung KIM
Journal of the Korean Pediatric Society 1982;25(9):935-943
No abstract available.
Anus, Imperforate*
7.Combination Chemotherapy with High Dose Cisplatin - Cyclophosphamide in Primary Epithelial Ovarian Cancer.
Jeong Sup YUN ; Ha Jeong KIM ; Sung Kyoo JANG ; Ki Hyung KIM ; Man Soo YOON
Korean Journal of Gynecologic Oncology and Colposcopy 2001;12(1):12-22
OBJECTIVE: The purpose of this study was to evaluate the therapeutic efficacy and toxicity of high dose cisplatin-cyclophosphamide combination chemotherapy on patients with primary epithelial ovarian cancer. METHODS: A review of 63 patients previously diagnosed as primary epithelial ovarian cancer after initial operation and histology at Pusan National University Hospital from Jul. 1993 to Jun, 1997 was performed. Patients were received the combination chemotherapy including cisplatin 100mg/m2/day and cyclophosphamide 750mg/m2/day, repeated 6 cycles every 4 weeks. The mean age was 48 years old, and previous surgical procedures were total abdominal hysterectomy and bilateral salpingo-oophorectomy with omentectomy. The patients were classified into FIGO stage and pathologic results. RESULTS: The clinical response rate was 100% in the FIGO stage Ic patients with PC combination chemotherapy, 100% in stage II, 53.5% in stage III, and 25% in stage IV. The overall response rate was 69.8%. The 3-year survival rate according to the treatment groups was 93.3% in stage Ic group, 60% in stage II, 50% in stage III and 0% in stage IV. The mean survival duration was 34.6 months. Hematologic toxicities in cisplatin-cyclophosphamide chemotherapy were neutropenia and anemia. Nausea and vomiting were the most common side effects and occurred in 96.8%. Most of the toxicities were grade 1 and 2. CONCLUSION: The combination chemotherapy with cisplatin-cyclophosphamide is relatively safe and effective method in the treatment of primary epithelial ovarian cancer.
Anemia
;
Busan
;
Cisplatin*
;
Cyclophosphamide*
;
Drug Therapy
;
Drug Therapy, Combination*
;
Humans
;
Hysterectomy
;
Middle Aged
;
Nausea
;
Neutropenia
;
Ovarian Neoplasms*
;
Survival Rate
;
Vomiting
8.Mediastinal parasitic cyst by paragonimiasis.
Ki Ho SONG ; Man Jong BAEK ; Kyung SUN ; Kwang Taik KIM ; In Sung LEE ; Hyoung Mook KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 1993;26(1):67-69
No abstract available.
Paragonimiasis*
9.Thoracic outlet syndrome: one case report.
Hong Suk KIM ; Doo Yun LEE ; Hae Kyoon KIM ; Ki Man BAE
The Korean Journal of Thoracic and Cardiovascular Surgery 1991;24(12):1192-1196
No abstract available.
Thoracic Outlet Syndrome*
10.Comparison Between HLA-DR Serological Typing and O1igotyping.
Jai Ho WEE ; Ki Cheol JEONG ; Tai Gyeom KIM ; Jin Yeong HAN ; Jeong Man KIM
Korean Journal of Clinical Pathology 1997;17(6):1089-1099
BACKGROUND: In renal transplantation, a good HLA-DR match Is associated with successive graft outcome. But due to a number of technical problems, reliable serological DR typing cannot always be obtained. To compare the serological DR typing with DRBI DNA typing, we tested 103 specimens that had been frozen after serological typing, by PCR-SSOP typing method. METHODS: Serological DR typing was performed by complement-dependent microlymphocytotoxicity technique using commercial antisera kits, and DNA gyp ins was performed by PCR-SSOP, using one of the methods recommended by 12th International Histocompatibility Workshop. DNA amplification was done by DRBAMP-A and DRBAMP-B primers, and hybridization by 18 oligonucleotides labelled with digoxigenin.. RESULTS: The concordance rate between serologic typing and DNA typing was 76.7%. Most (79.0%) of discordant results were due to serological blanks turning out to be definable antigens by DNA typing and these antigens consisted of mainly DR5 splits but none of DR1, DR2, or DR7. CONCLUSIONS: In spite of technical improvement, serological typing method often can not define the accurate HLA-DR type. It is thought that combining serological typing with DNA typing Is necessary to achieve a higher success rate of graft outcome.
Digoxigenin
;
DNA
;
DNA Fingerprinting
;
Education
;
Histocompatibility
;
HLA-DR Antigens*
;
Immune Sera
;
Kidney Transplantation
;
Oligonucleotides
;
Transplants