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이진배(Jinbae Lee),오해석(Haeseok Oh) 한국정보과학회 1995 한국정보과학회 학술발표논문집 Vol.22 No.1
본 논문에서는 CCD 카메라로 입력된 차량영상에서 번호판을 인식하는 방법을 제안한다. 기존의 연구결과들은 입력된 영상의 질, 번호판 영역의 완전성 등에 대하여 많은 제한사항들을 가지고 있었다. 본 연구에서는 기존의 번호판 인식시스템들이 가지고 있는 여러 제한 사항들, 즉 낮은 콘트라스트의 화상을 인식하지 못하는 것, 촬영 위치가 정면에서 벗어 날 수 없는 것, 또 주행중인 차량에 대해서 적용 할 수 없다는 문제점들을 해결책을 제시하고자 한다.
임신 중 발견되어 말기 신부전으로 진행한 수질낭성 신질환 1 예
박민식(Min Sik Park),이진배(Jin Bae Lee),임상혁(Sang Hyuk Lim),안기성(Ki Sung Ahn),이인희(In Hee Lee) 대한신장학회 2002 Kidney Research and Clinical Practice Vol.21 No.5
Medullary cystic disease (MCD) and familial juvenile nephronophthisis are inherited diseases characterized by development of small cysts at the corticomedullary borders of the kidneys. Both diseases consist of microscopic or gross cysts of the renal medullae associated with atrophy of nephrons, anemia, renal insufficiency, polyuria, and salt-wasting. We report a 27-year-old pregnant female patient with MCD which caused acute renal failure progressing to end stage renal disease during the second trimester. Hypertension, oliguria, preeclampsia, placenta abruptio, and disseminated intravascular coagulation were also accompanied. Radiologically, abdominal ultrasonography and computed tomogram showed many cysts confined only to the renal medullae, which are typical findings consistent with MCD. In spite of conservative therapy, her renal function deteriorated rapidly and uremic symptoms including pulmonary edema were aggravated. She was started on hemodialysis and she has received regular hemodialysis without recovery of renal function.
갈색세포종이 동반된 신경섬유종증 1형에서 발생한 자발성 뇌출혈1예
김무곤 ( Moo Gon Kim ),이진배 ( Jin Bae Lee ),홍승표 ( Seung Pyo Hong ),김소연 ( So Yern Kim ),이영수 ( Young Soo Lee ),류재근 ( Jae Kean Ryu ),최지용 ( Ji Yong Choi ) 대한내과학회 2008 대한내과학회지 Vol.75 No.1
신경섬유종증 환자에서 갈색세포종이 동반된 경우는 약 0.1~5.7%에 이르나, 자발성 뇌출혈은 매우 드문 합병증이다. 저자들은 신경섬유종증 1형의 임상적인 특징을 보이는 30세 여자가 고혈압과 자발성 뇌출혈로 내원하였고 항고혈압제로 혈압이 조절되지 않아 뒤늦게 갈색세포종이 진단되어 수술적으로 치료한 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다. Spontaneous intracerebral hemorrhage is very rare in patients with neurofibromatosis type 1. A 30-year-old woman was referred to our hospital for evaluation of headaches, nausea, and vomiting. She was diagnosed with neurofibromatosis type 1 and a spontaneous intracerebral hemorrhage. She was treated with conservative management, including antihypertensive medications for 32 months. However, because of sustained hypertension, we performed screening tests for a pheochromocytoma. The 24 hr urine VMA and urine metanephrines were elevated. Abdominal CT showed a right adrenal mass, 7.5×5.8 cm in size. After a successful resection of the tumor, the hypertension resolved without medication for >1year. This case illustrates that delayed diagnosis and treatment of pheochromocytoma can cause serious complications from hypertension, such as cerebrovascular hemorrhage. Thus, in patients with neurofibromatosis and hypertension, screening for pheochromocytoma is important for the early detection of an adrenal tumor. (Korean J Med 75:103-107, 2008)
정승혜 ( Seung Hie Chung ),이진배 ( Jin Bae Lee ),임상혁 ( Sang Hyuk Lim ),김채기 ( Chae Gi Kim ),최정윤 ( Jung Yoon Choe ) 대한류마티스학회 2002 대한류마티스학회지 Vol.9 No.4
Overlap syndrome is used to describe patients who have two or more well-defined connective tissue diseases. Although a variety of overlap syndromes are now recognized, the coexistence of the progression of juvenile rheumatoid arthritis (JRA) to systemic lupus erythematosus (SLE) is uncommon. We describe a patient who had typical deforming polyarthritis, who years later developed SLE.