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박봉림(BL Park),김관옥(KO Kim),김규관(KG Kim),박건남(KN Park),장준홍(JH Jang),김동진(DJ Kim) 대한산부인과학회 1987 Obstetrics & Gynecology Science Vol.30 No.9
저자들은 본병원 산부인과에서 30세의 경산부에서 자궁간질선근종증 1례를 체험하였기에 문헌고찰과 함께 보고하는 바이다. Endolymphatic stromal myosis of the uterus is a unusual mensenchymal tumor, originating in the endometrium. There has been considerable controversy as to nomenclature because of the uncertainty of the cell of origin and the behavior of the tumor. Here a case of a 30-year old woman with a endolymphatic stromal myosis is presented with a review of literatures.
혈우병 A의 효율적 진단을 위한 한국인의 St14 VNTR 다형현상에 대한 Southern 및 PCR-RELPs 분석
박봉림(BL Park),이춘근(CK Lee),조율희(YH Cho),정성노(SR Chung),박문일(MI Park),문형(H Moon),황윤영(YY Hwang) 대한산부인과학회 1996 Obstetrics & Gynecology Science Vol.39 No.9
One of the extragenic polymorphic markers of coagulation factor VIII gene, a VNTR locus St14(DXS52) was investigated to determine the degree of the polymorphism in Koreans and evaluate the usefulness in prenatal diagnosis of Hemophilia A through Southern and PCR-RELPs analysis. In Southern analysis of 151 X chromosomes(49 males and 51 females), the hybrid probe called F814 detects in BclI digests both the St14(DXS52) multiallelic polymorphism and FVIII RFLP. Although the exact allelic frequency of multiallelic polymorphism could not be determined due to incomplete separation of multiple alleles, but most of alleles were clearly discernible this polymorhpic system. The female heterozygote rate of this probe was 84%. It is noticeable that the distribution pattern of multialleles was well corresponded to the PCR results of this locus. A total of 15 alleles were detected in PCR amplification of VNTR locus St14. The allele distribution patterns were different from those previously reported in Caucasian males. The polymorphism information content(PIC) of this locus was 78%. Digestion of the PCR products of this locus with TaqI revealed the presence of a polymorphic TaqI restriction site within the product 200 bp from the end. This restriction site present on 92.2%and absent on 7.8% of all alleles, but the absence is confined soley to the alleles 1690 bp(6.5%) and 2470 bp(1.3%).Determination of this polymorphism within St14 VNTR region increase the expected heterozy-gosity about 16% and 50% in homozygotes of alleles 1690 bp and 2470 bp, respectively. The above results indicate that analysis of St14 VNTR locus give more accurate informations than Southern analysis, but the probe F814 increase the informativity by sinultaneous detection of FVIII intragenic polymorphism. It is concluded that about 80% of Hemophilia A families in Korean population can be successfully and efficiently diagnosed when using Southern or PCR-RFLPs analysis of St14 VNTR locus for the carrier detection and prenatal diagnosis of hemophilia A.
Female Precocious Pseudopuberty를 동반한 난소과립막세포종의 1 례
김관옥(KO Kim),박봉림(BL Park),김규관(KG Kim),박건남(KN Park),김동진(DJ Kim) 대한산부인과학회 1988 Obstetrics & Gynecology Science Vol.31 No.6
Female Precocious Pseudopuberty를 동반한 난소과립막세포종 Functional ovarian tumors is the rare disease among ovarian tumors and is considered from granulosa cell origin. It was usually diagnosed after menopause, but was diagnosed infrequently before puberty. We had experiencd one case of functional ovarian tumors in 3 and 11/12 year-old female child, surgicla removal was performed and proved the juvenile granulosa cell tumor. Now, we present it with the brief review of literatures.