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김관용 ( Kwan-yong Kim ),심영수 ( Young-su Shim ),정호진 ( Ho-jin Jeong ),김승진 ( Seung-jin Kim ),박주형 ( Joo-hyung Park ) 한국정보처리학회 2023 한국정보처리학회 학술대회논문집 Vol.30 No.2
본 논문에서는 무료 Git 저장소로 전 세계 1억 명 이상의 IT개발자가 사용하는 Github[1]의 commit 수와 issue 해결 등의 사용 시 토큰을 차등 부여해 사용자 종합 순위를 선정하고 정량적인 성취 수준을 파악할 수 있는 시스템을 마련해 개발자들의 건전한 경쟁심과 개발 욕구를 향상시키는 애플리케이션을 개발하였다.
우리나라 성인여성에서 정상 폐활량 예측을 위한 양팔벌린 손끝길이와 신장과의 관계
고원중 ( Won Jung Koh ),주영수 ( Young Su Ju ),김태엽 ( Tae Yub Kim ),박재성 ( Jae Sung Park ),유승도 ( Seung Do Yu ),최광수 ( Kwaung Soo Choi ),백도명 ( Do Myung Paek ),한성구 ( Sung Koo Han ),심영수 ( Young Soo Shim ) 대한결핵 및 호흡기학회 1999 Tuberculosis and Respiratory Diseases Vol.46 No.6
이재철,김영환,이승준,심영수,한성구,유철규,김계수 대한내과학회 1997 대한내과학회지 Vol.53 No.4
Necrotizing sarcoid granulomatosis was first described by Liebow, who included it in the category of pulmonary angiitis and granulomatosis. Wegener`s granulomatosis and limited Wegener`s granulomatosis are also included in this category. Necrotizing sarcoid granulomatosis is characterized by histologically sarcoid-like granulomata, prominent and granulomatous vasculitis, and varying degrees of necrosis, radiographically pulmonary nodules but no enlarged hilar lymph nodes, clinically benign course. Whether this entity is a variant of necrotizig vasculitis with sarcoid reaction or sarcoidosis with prominent vascultic features and necrosis is not yet, clear, but many authors suggest the relationship with sarcoidosis from the observation of the similarity of histologic features and clinical course between the two entities. Patients are asymptomatic in about one fourth. Even symptomatic patients have vague symptoms such as cough, chest pain. Extrapulmonary involvement is rare. The prognosis is good even without therapy or with steroid alone, if necessary. We report a case that was diagnosed by open lung biopsy as necrotizing sarcoid granulomatosis, and it is assumed to be the first report of this entity in Korea.
골수를 포함한 다발성 장기 침윤을 나타낸 유육종증(Sarcoidosis) 1 예
이재철,김영환,이승준,김재열,심영수,한성구,유철규,김계수,남송현 대한내과학회 1997 대한내과학회지 Vol.53 No.4
Sarcoidosis is a multisystem granulomatous disorder commonly affecting young adults. Diagnosis is confirmed by evidence of non-caseating granuloma in more than one organ. A case is presented where the diagnosis was made on a bone marrow biopsy, the first case in Korea. A 54-year-housewife was admitted because of multiple variable sized, skin papules and macules, who showed pancytopenia and evidence of liver cirrhosis on ultrasound. We performed skin biopsy and bone marrow biopsy, which showed non-caseating granulomas. The chest CT, opthalmologic examination was performed and showed the involvement of sarcoidosis of mediastinal lymph nodes and uvea. Multiple joints of both hands and feet also seemed to be involved in view of simple X-ray. By this case, we emphasize the significance of bone marrow biopsy in the sarcoidosis with pancytopenia.