http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
- 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
- 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
RISS 인기검색어
- 검색키워드
- 저자 : 박소양 ( So Yang Park ) (검색결과 7 건)
- 무료
- 기관 내 무료
- 유료
-
박소양(So-Yang Park) 현대미술사학회 2005 현대미술사연구 Vol.18 No.-
My thesis explores the history and psychology of the Minjoong(grassroots) Realist Art and Culture Movement which emerged during the democratisation period in South Korea in the 1980s and early 1990s. Following territorial decolonization and 35 years of rapid industrialisation led by the military dictatorial regime, the 1980s and the 1990s markeda time of insurgence of popular antagonism against the regime and the dominant norms of society which had repressed the expressions of the grassroots people in the society. I examine how the emergent culture a 'visual culture of haunting' is instigated and formed by numerous haunted subjects and the return of repressed memories. This culture is marked by works of Lim Oksang and Oh Yoon who materialised the ghosts of the minjoong, who had long been repressed by "silencing structure" and "culture of forgetting" of Korean society. They actively dealt with the personal and historical trauma and haunting imagination of a future as part of the incorporation process of the internal images of "the Real". The 'Real' translates the irreducible core of memory and imagination of the minjoong which has previously unrepresented.
-
박은선(Eun Sun Park),김미란(Mi Ran Kim),김현진(Hyun Jin Kim),강은주(Eun Joo Kang),박소양(So Yang Park),강경화(Kyeng Hwa Kang) 대한산부인과학회 2000 Obstetrics & Gynecology Science Vol.43 No.9
Round ligament pregnancy is very rare form of extrauterine pregnancy and life threatening variant of ectopic pregnancy with high maternal mortality.The incidence ranges from 1/49000 to 1/184000 pregnancies.The clinical characteristics of round ligament pregnancy is variable, and the diagnosis is rarely made preoperatively.We have experienced a case of round ligament pregnancy in a 37-year-old woman and report it with brief review of literatures.
-
양수진(Su Chin Yang),조은나(Eun Na Cho),박소양(So Yang Park),김미희(Mi Hee Kim),김병점(Pyung Jum Kim) 대한산부인과학회 2002 Obstetrics & Gynecology Science Vol.45 No.2
Spontaneous uterine rupture during the second trimester of pregnancy is a rare obstetric emergency. When a patient presents with acute abdominal pain and signs of hemorrhagic shock, a number of differential diagnoses must be considered. Early diagnosis and proper management is necessary to decreased the high maternal and fetal morbidity and mortality associated with rupture of uterus. We present a case of spontaneous rupture of the uterus in the 18th week of pregnancy with a brief review of literatures.
-
김미희 ( Mi Hee Kim ),양수진 ( Su Chin Yang ),조은나 ( Eun Na Cho ),박소양 ( So Yang Park ),안현숙 ( Hyun Sook An ),최원영 ( Won Young Choi ) 대한산부인과학회 2002 Obstetrics & Gynecology Science Vol.45 No.9
전전뇌증은 태생기 전뇌의 게실화의 실패로 인한 전두부의 기형복합체이다. 전전뇌증의 조기 산전 진단은 심한 증도를 밝혀내고, 예후를 예상하고, 그 예후 및 심한 정도에 따라 적절한 치료를 결정하기 위해 중요하다. 최근 고해상 초음파의 발달로 임신 초기에 전전뇌증을 가진 태아의 발견이 가능해졌다. 우리는 산전에 진단된 무엽성 전전뇌증 1예를 초음파 및 부검 소견과 함께 보고하는 바이다. Holoprosencephaly is a complex abnormality of the forebrain that is postulated to derive from a failure in the diverticulation of the embryonic prosencephalon. Early antenatal diagnosis of holoprosencephaly is important to find out its severity, to predict its prognosis and to determine proper treatment according to its prognosis and severity. With recent development of high resolution ultrasonography, it is possible to detect a fetus with holoprosencephaly at early antenatal period. We report a case of alobar holoprosencephaly, diagnosed antenatally with its sonographic and autopsy finding.
-
김현진(Hyun Jin Kim),이승무(Seung Moo Lee),김은정(Eun Jeong Kim),조은나(Eun Na Cho),박소양(So Yang Park),강경화(Kyung Hwa Kang),박숙자(Sook Ja Park) 대한산부인과학회 2001 Obstetrics & Gynecology Science Vol.44 No.6
N/A Objectives: To analyze 2942 cases of prenatal genetic amniocentesis with their cytogenetic results. Methods: This study reviewed 2942 genetic amniocentesis results which were perfomed at Ilsin Christian Hospital from 1993 to 1999, as prenatal genetic diagnosis for the possibility of chromosomal abnormality of fetus. Age distribution, gestational weeks, indications of amniocentesis and cytogenetic results were the key factors for the analysis. Results: Maternal ages were ranged from 20 to 45, mostly 25-39. Of indications of prenatal genetic amniocentesis, abnormal maternal serum marker was the most common(S7.9%) and followed by advanced maternal age(29.3/a). The frequency of abnormal karyotypes was 3.1%(90/2942). Down syndrome(trisomy 21) and inversion of chromosome were found at 0.8%(24/2942) and 1.0%(30/2942). The incidence of abnormal karyotype according to indication had statistieal significance in family history and abnormal ultrasonographic findings. (p < 0.001) Conclusions: Midtrimester genetic amniocentesis is an important diagnostic tool in prenatal genetic diagnosis. In addition to the maternal serum markers and maternal ages, complete family history takings and ultrasonograms should be considered in prenatal genetic counseling.
-
이혜정,김수연,박소양,표철우,한훈,양일호 대한조혈모세포이식학회 2002 대한조혈모세포이식학회지 Vol.7 No.1
연구배경: HLA-class I 유전자는 높은 다양성을 가지고 있다. 장기이식 시 GVHD 유발에 많은 영향을 끼치는 것으로 알려져 있는 HLA-B locus는 258개의 대립유전자가 존재한다고 알려져 있으며 대부분 exon 2, 3 부위에 다형성을 갖는다. 방법: 대립유전자형을 구분하는 방법으로는 항원 항체반응을 이용한 혈청학적 방법이 주로 사용되어 왔으나 최근에는 분자생물학적인 방법들이 개발되어 이용되고 있다. 한국인에서는 HLA-B49, B50, B18, B45, B73 등이 존재하지 않는다고 알려져 있으나 DNA수준에서의 HLA-대립유전자형 형별이 가능해지고 형별대상의 수가 축적됨에 따라 과거 한국인에서 볼 수 없었던 대립유전자형이 검출될 것으로 예상된다. 결과: 혈청학적인 방법과 ARMS-PCR 방법에 의해 밝혀진 제대혈액의 HLA-B homozygote가 진정한 homozygote인가를 규명하기 위한 연구 도중에 한국인에서는 존재하지 않는다고 알려져 있던 HLA-B*4901을 direct sequencing으로 확인할 수 있었다. 결론: HLA 형별 결과가 장기 생존율 및 GVHD 발생에 영향을 미치는 조혈모세포이식이 증가되고 있으므로, 각 locus별로 blank이거나 homozygote인 경우에는 DNA수준의 HLA-대립유전자형별이 필수적이다. Background: HLA (human leukocytes antigens)-class I genes are highly polymorphic, play many roles in organ and bone marrow transplantain. HLA-B is the most polymorphic in exon 2 and exon 3 of class I locus with 258 alleles. Methods: Until recently, HLA-class I typing has been mainly based on serologic methods. The development of molecular biological techniques make it possible to define the genotypes in HLA genes. HLA-B49, B50, B18, B45, B73 alleles which have been known to be rare or absent in Korean are expected to be found by both the development of HLA genotyping at the DNA level and the accumulation of HLA data. Results: HLA-B genotyping by direct sequencing was performed on cord blood sample which HLA-B serotype was homozygote or blank by ARMS-PCR method. We found HLA- B*4901 allele which was rare in Korean. Conclusion: In order to increase the successful frequencies of stem cell transplantation, HLA genotyping at the DNA levels are necessary in case of blank or homozygous loci.
-
김미희,양수진,조은나,박소양,안현숙,최원영 대한산부인과학회 2002 Obstetrics & Gynecology Science Vol.45 No.11
전전뇌증은 태생기 전뇌의 게실화의 실패로 인한 전두부의 기형복합체이다. 전전뇌증의 조기 산전 진단은 심한 증도를 밝혀내고, 예후를 예상하고, 그 예후 및 심한 정도에 따라 적절한 치료를 결정하기 위해 중요하다. 최근 고해상 초음파의 발달로 임신 초기에 전전뇌증을 가진 태아의 발견이 가능해졌다. 우리는 산전에 진단된 무엽성 전전뇌증 1예를 초음파 및 부검 소견과 함께 보고하는 바이다. Holoprosencephaly is a complex abnormality of the forebrain that is postulated to derive from a failure in the diverticulation of the embryonic prosencephalon. Early antenatal diagnosis of holoprosencephaly is important to find out its severity, to predict its prognosis and to determine proper treatment according to its prognosis and severity. With recent development of high resolution ultrasonography, it is possible to detect a fetus with holoprosencephaly at early antenatal period. We report a case of alobar holoprosencephaly, diagnosed antenatally with its sonographic and autopsy finding.
KCI
DBpia연관 검색어 추천
이 검색어로 많이 본 자료
활용도 높은 자료
