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무선센서 네트워크 환경에서 지연 및 신뢰성을 고려한 클러스터 기반의 라우팅 알고리즘
심명숙 ( Myung-sook Shim ),박명순 ( Myong-soon Park ) 한국정보처리학회 2010 한국정보처리학회 학술대회논문집 Vol.17 No.1
본 논문에서는 선형적인 무선 센서 네트워크에서 지연 및 신뢰성을 고려한 클러스터 기반의 멀티홉 라우팅 알고리즘을 제안한다. 제안한 알고리즘은 선형적인 네트워크 환경에서 전송 지연시간 및 Single Point Of Failure 를 해결하기 위해 짝수 ID 노드일 경우 다음 짝수 ID 노드로 전송하고, 홀수 ID 노드일 경우 다음 ID 노드로 데이터를 전송하는 방법을 사용한다.
중학교 수학과 도형영역에서의 교과서 재구성에 관한 효율성 연구
심명숙,전재복 국민대학교 2002 기초과학연구소 논문집 Vol.21 No.-
The study was conducted by choosing, applying, and testifying the following research questions. 1. How do 40 math ematics teachers of Mathematics 7-B step of middle schools in S-district in Seoul understand the problem regarding textbook recomposition? And what is the result of its application? 2. What is the difference in student understanding between the comparison groups, where the text book was recomposed according to the topics in the 7th education curriculum mathematics textbook and where the instruction was applied according to the order of mathematics textbook of the 7th education curriculum. 3. What is the difference in terms of definition area between the comparison groups where the textbook was recomposed according to the topics in the 7th education curriculum mathematics textbook and where the instruction was applied according to the order of mathematics textbook of the 7th education curriculum?
양측성 잠복고환과 당뇨를 동반한 Prader-Willi 증후군 1예
김미진,심명숙,신영구,정춘희,정현숙,김상하,윤상진,장기웅,장인영,이병준,양영호,김성진 대한내과학회 2002 대한내과학회지 Vol.63 No.4
Prader-Willi syndrome (PWS) is a complex, multisystem disorder comprising congenital hypotonia, feeding difficulties, hypogonadism and hypogenitalism, short stature, small hands and feet, mental and psychomotor retardation, distinctive facial appearance, onset of obesity in early childhood and a tendency to develop glucose intolerance in adolescence. Yet the syndrome remains difficult to diagnose due to the subtle nature of many of the manifestations. We report an 19-year old man with PWS, confirmed by fluorescence in situ hybridization (FISH) with DNA probes specific for the PWS region on chromosome 15.
이재명,정춘희,신영구,심명숙,김영욱 대한내분비학회 2001 Endocrinology and metabolism Vol.16 No.1
The 46, XX male syndrome is rare disease that is characterized by a phenotypic male who has a 46, XX female karyotype. Since the first report by de la Chapelle and associates in 1964, several cases have been reportc4 but it is still a rare entity. Recently we examined a 20-year-old XX male who had the symptoms of gynecomastia, an infantile appearance of the external genitalia, scanty pubic hair, no Adams apple, and no axillary hair. We presently describe a patient with the 46, XX male syndrome who showed a 46, XX karyotype on chromosomal study and review the literatures (J Kor Soc Endocrinol 16:148-152, 2001).