http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Fitz - Hugh Curtis 증후군과 동반된 자궁부속기 방선균증 1 예
윤선웅(Seon Woong Yoon),이정훈(Jeong Hoon Lee),김형문(Hyoung Moon Kim),김계현(Kye Hyun Kim),이교원(Kyo Won Lee),한종설(Jong Sul Han),김성도(Sung Do Kim),이상준(Sang Joon Lee),김명숙(Myung Sook Kim) 대한산부인과학회 2001 Obstetrics & Gynecology Science Vol.44 No.6
Actinomycosis is a chronic suppurative and granulomatous disease. Actinomyces is a gram positive, anaerobic and non-acid fast bacterium. Many actinomycotic pelvic infection in women used intrauterine device(IUD) with long duration were reported, in contrast, others suggest that actinomycosis develop opportunistic infection irrespective of intrauterine device. One to ten percents of patients with acute pelvic inflammatory disease(PID) develop perihepatic inflammation and adhesion--the Fitz-Hugh-Curtis syndrome. Although in the past Neisseria gonorrhea was thought to be the only etiological agent, recent data indicate that chlamydia trachomatis produces the majority of cases. We have experienced the case of tubo-ovarian actinomycosis(case with IUD(Cu-T)) associated with Fitz-Hugh-Curtis syndrome in a 29years old woman, and reported that with a review of related literatures.
융모막 세포에서 다중중합효소 연쇄반응을 이용한 Duchenne형 근이영양증의 산전 진단
이교원(Kyo Won Lee),윤선웅(Seon Woong Yoon),장우섭(Woo Sup Chang),김진영(Jin Yeong Kim),이숙환(Sook Hwan Lee),이상준(Sang Joon Lee),김성도(Sung Do Kim),한종설(Jong Sul Han) 대한산부인과학회 1999 Obstetrics & Gynecology Science Vol.42 No.9
Objective: To evaluate the efficacy of prenatal multiplex PCR with chorionic villi, in the case of family history of DMD due to exon deletion. Methods: DNA was extracted when cells' size are 1x 106 on T- flask surface area reach to 25 cm2 after 2 weeks from sex confirmation. Average DNA concentration was 50-100 ng and multiplex PCR test was performed from DNA extraction. Result: PCR was done for 17 exons devided into 4 groups. Seventeen exons were all amplified with their right size. Conclusions: This method is DNA analysis for prenatal diagnosis of DMD with chorionic villi in the family of DMD. This is useful when preimplantation genetic diagnosis is not available.
조현구(Hyun Gu Cho),윤선웅(Seon Woong Yoon),이대남(Dae Nam Lee),이교원(Kyo Won Lee),한종설(Jong Sul Han),김성도(Sung Do Kim),이상준(Sang Joon Lee) 대한산부인과학회 2001 Obstetrics & Gynecology Science Vol.44 No.4
Cerebrovascular disease refers to disorder of one or more blood vessels of the brain, and the majority of lesions that arise from these are from arterial diseases. The occurrence of cerebral venous thrombosis is clearly linked to the puerperal state, and pregnancy may increase the risk of subarachnoid hemorrhage. The most common cause is rupture of arterial aneurism. Hemodynamic, hormonal or other physiological changes of pregnancy may play a role in aneurysmal rupture. We report two cases of cerebrovascular diseases in the puerperium with a brief review of concerned literatures.
한국인 다낭성 난포증후군 환자에서 5,10-Methylenetetrahydrofolate Reductase의 677번 유전자 다형성에 관한 연구
이교원,정유미,이숙환,윤태기,곽인평,윤선웅,최중섭,김계현,한종설,김성도,김남근,차광렬,백광현,이수만,Lee, Kyo-Won,Jeong, Yu-Mi,Lee, Sook-Hwan,Yoon, Tae-Ki,Kwak, In-Pyung,Yoon, Seon-Woong,Choi, Joong-Sub,Kim, Kye-Hyun,Han, Jong-Sul,Kim, Sung-Do,K 대한생식의학회 2003 Clinical and Experimental Reproductive Medicine Vol.30 No.3
Objective: To investigate the association of genetic background between MTHFR C677T genotype and infertile females with polycystic ovarian syndrome. Materials and Methods: We compared 86 infertile females with polycystic ovarian syndrome (PCOS) with 100 healthy fertile females with one or more offspring. Pyrosequencing analysis for MTHFR C677T variation was performed on polymerase chain reaction (PCR) product of study group. To validate pyrosequencing data of C677T variation for randomly selected 50 samples, we compared the pyrosequencing result with the PCR-RFLP (Restriction Fragment Length Polymorphism) result of MTHFR C677T genotype. Results: The prevalence of the C677T mutant homozygous (TT) was significantly lower (p=0.0085) in females with PCOS (8.14%) than in fertile females (21.00%). MTHFR 677 TT genotype had a decreased risk (3.7-fold) of PCOS compared with wild type (MTHFR 677 CC). Conclusion: Our data support a role for MTHFR mutant homozygous (677 TT) genotype in reducing risk in Korean infertile females with Polycystic ovarian syndrome.
복강경하 질식 전자궁적출술 (LAVH) 154예의 임상적 고찰
김형문 ( Hyoung Moon Kim ),신인환 ( In Whoan Shin ),윤선웅 ( Seon Woong Yoon ),최중섭 ( Joong Sub Choi ),김계현 ( Kye Hyun Kim ),이교원 ( Kyo Won Lee ),김성도 ( Sung Do Kim ),한종설 ( Jong Sul Han ) 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.8
Objective: To evaluate the indications, advantages and complications of laparoscopically assisted vaginal hysterectomy (LAVH), retrospectively. Methods: From Mar. 2003 to Feb. 2004, clinical trials of LAVH (n=154) were performed in the Department of Obste