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심한 방광 요관 역류를 동반한 양측성 Hutch's Diverticulum 1례
신종수,전유식,나창수,정건영,염규영,Shin Jong-Su,Jeon Yu-Sik,Ra Chang-Soo,Jeong Gun-Young,Yeum Gyu-Young 대한소아신장학회 1998 Childhood kidney diseases Vol.2 No.1
A bladder diverticulum occurs when the bladder mucosa herniates or protrudes through the muscular wall of the baldder. The majority of congenital bladder diverticula occurs in males. They are the most common in the region of the bladder base, most frequently in the region of the ureteral hiatus, in which case they are known as Hutch's diverticula. They can give rise to obstruction or reflux. We had experienced a case of bilateral Hutch's diverticulum associated with vesicoureterai reflux in a 23 month old male. Chief complaints were urinary frequency and dysuria. Voiding cystourogram and CT scan revealed large bilateral Hutch's diverticulum with bilateral vesiciureteral reflux grade VI. There was evidence of urinary infection. This patient was successfully treated by ureteroneocystostomy. We report this case with a brief review of related literatures.
신종수 ( Jong Soo Shin ) 한국콩연구회 2013 韓國콩硏究會誌 Vol.29 No.1
The objectives of this report are to provide business strategy model for small & mid scale soy processing companies by sharing the successful business development strategies (material sourcing, production and marketing) of mid scale soymilk company.
신종수(Jong Soo Shin),이문정(Moon Jeong Lee),김성환(Sung Hwan Kim) 대한소아신경학회 2014 대한소아신경학회지 Vol.22 No.3
Glucose transporter type 1 deficiency syndrome (GLUT1-DS) is caused by impaired glucose transport across the blood-brain barrier (BBB) and characterized by infantile seizures, developmental delay, acquired microcephaly, spasticity, ataxia, and a low cerebrospinal glucose concentration (hypoglycorrhachia). A diagnosis of GLUT1-DS is biochemically established in neurologically impaired patients with hypoglycorrhachia in the normoglycemia. GLUT1-DS can be confirmed by mutation analysis of the solute carrier family 2 (facilitated glucose transporter), member 1 (SLC2A1) gene or reduced 3-O-methyl-D-glucose uptake into erythrocytes. The patient was a 12-year-old boy born at term. He had experienced seizures from 4 months of age. Electroencephalography (EEG) did not show epileptiform activity. Brain magnetic resonance imaging (MRI) revealed mild diffuse cortical atrophy and ventricular dilatation. Furthermore, he showed developmental delay, mental retardation, and ataxia, which all became more apparent with age progression. For 7 years, he had experienced paroxysmal episodes of atonic behavioral changes that were aggravated before meals or when he became tired. When he was 12 years old, cerebrospinal fluid (CSF) analysis revealed a low glucose concentration in the normal serum glucose and lactate levels. Under the impression of GLUT1-DS, mutation analysis of the SLC2A1 gene by direct sequencing was performed using white blood cells, and c.680-2delA of intron 5 was found. We describe a GLUT1-DS patient with a typical natural history of GLUT1-DS through a long term follow-up visits, with a novel splice site mutation (SLC2A1: c.6802delA).
신종수(Jong-soo Shin),김문정(Moon Jeong Kim),엄영익(Young Ik Eom) 한국정보과학회 2002 한국정보과학회 학술발표논문집 Vol.29 No.2Ⅲ
최근 인터넷의 사용자 증가와 함께 사용자들의 요구는 다양해지고 있다. 또한 멀티미디어 컨텐츠도 사용자의 요구에 따라 점차 대용량화되고 있다. 멀티미디어 서비스 제공자는 사용자의 다양한 요구들 충족시키기 위해서 대용량 고품질의 컨텐츠를 많이 보유하고 있어야 한다. 그러나 클라이언트-서버 환경에서 대용량의 멀티미디어 컨텐츠 서비스를 제공하기 위해서는 고성능의 컴퓨터가 필요하다. 게다가 컨텐츠의 양과 사용자의 수가 증가함에 따라 중앙 서버로 부하가 집중되고, 신뢰성이 떨어진다는 문제점도 있다. 본 논문에서는 중앙으로 집중되는 요청을 분산시키고 대용량의 멀티미디어 컨텐츠를 저장하기 위해서 각 컴퓨터들을 P2P환경으로 구축하고, 이동 에이전트를 이용하여 분산된 멀티미디어 컨텐츠를 검색하는 기법을 제시한다.
이현교 ( Hyun Kyo Lee ),송태준 ( Tae Jun Song ),최종욱 ( Jong Wook Choi ),하소영 ( So Young Ha ),김정욱 ( Jung Wook Kim ),신종수 ( Jong Soo Shin ),김철남 ( Chul Nam Kim ),장선희 ( Sun Hee Chang ) 대한췌장담도학회 2015 대한췌담도학회지 Vol.20 No.3
Gastrointestinal bleeding from the biliary tree, called hemobilia, is an uncommon event. It may clinically present as hematemesis or melena. Ruptured cystic artery pseudoaneurysm is a rare cause of hemobilia, with 2 cases reported in Korea. We present this unusual condition in a 65-year-old man whose chief complaint was abdominal pain. His final diagnosis was ruptured cystic artery pseudoaneurysm, and he was successfully treated by transcatheter arterial embolization and laparoscopic cholecystectomy.