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서병관,류성룡,이송실,허정은,백용현,이재동,최도영,조윤제,김남재,박동석 WHO COLLABORATING CENTRE FOR TRADITIONAL MEDICINE 2004 東西醫學硏究所 論文集 Vol.2004 No.-
Objective : The aim of this study was to review systemically clinical trials on the effectiveness and safety of herbal medicines in the treatment of osteoarthritis. Methods : Computerized literature searches were carried out on seven electronic databases, and hand-searching on some chinese medical journals in library of Kyung Hee Medical Center. Trial data were extracted in a standardized, predefined manner and assessed independently. Results : 1. Thirty reports of clinical trials and two reports of meta-analyses concerning herbal medicine were collected and reviewed Among these reports three medical herbs were applied as topical medicine and others as internal medicine. 2. The western studies established NSAIDs or placebo as their control group. Five chinese reports established formulated herb pill(Ruanshnagshenjin pill) as their control group and Six did not establish a control group at all. 3. ACR was the most highly used diagnostic criteria in the western studies while the Chinese used their official criteria established by their government or the criteria of their text books. 4. 20 reports chose the Lequesne functional index, SHAQ, WOMAC OA index, AIMS, and their own unique scoring system as the criteria of analysing the effect. Others chose clinical symptoms, articular functions, and lab finding as their criteria. 5. 7 single herbs and 19 formulated herbs were studied. Among the formulated herbs, Achyranthes japonica was studied in 10 of the studies and Angelica gigantis Radix in 8, making them the most often studied herbs among the studies.
열성 이영양성 수포성 표피박리증 환자에서 전신마취를 통한 치과치료
조성현(Seong-Hyeon Cho),송제선(Je-Seon Song),이효설(Hyo-Seol Lee),최형준(Hyung-Jun Choi),최병재(Byung-Jai Choi),김성오(Seong-Oh Kim),이제호(Jae-Ho Lee) Asia association of Disability and Oral health 2012 대한장애인치과학회지 Vol.8 No.2
본 증례는 열성 이영양성 수포성 표피박리증을 가진 2세 8개월 된 환자로 다발성 우식증 소견을 보여 전신마취하에 치료하였다. 1. 환자는 열성 이영양성 수포성 표피박리증으로 전신에 흉터가 있었으며 심한 빈혈 및 패혈증 증상이 있어 수혈 및 항생제 등으로 먼저 전신상태를 회복하였다. 2. 전신마취하에 모든 절치의 발치 및 구치 부위의 치수 치료와 기성금속관 수복을 시행하였다. Epidermolysis bullosa (EB) is an inherited skin disease characterized by blister formation of the skin following just minor trauma or spontaneously. The main classification of EB is based on the localization of the blistering. In epidermolysis bullosa simplex, the blister formation is intraepidermal; in epidermolysis bullosa junctionalis the blister formation in the epidermal-dermal junction; in the dystrophic forms of EB blister formation is intradermal. Oral manifestations of recessive dystrophic EB are characterized by rampant caries, crowding, microstomia, ankyloglossia, vestibular obliteration. Dental therapy may be well provided to patient with recessive dystrophic EB by using general anesthesia especially in case of poor cooperation. A two years old girl with recessive dystrophic EB visited our clinic for rampant caries. She was hospitalized for severe anemia and fever, and we provided dental therapy under general anesthesia. Extraction of incisors and stainless steel crown restoration of primary molars were performed.
Diphenylhydantoin에 의한 중증 재생불량성 빈혈
김한성 ( Kim Han Seong ),한경근 ( Han Gyeong Geun ),김종현 ( Kim Jong Hyeon ),김경환 ( Kim Gyeong Hwan ),조강일 ( Jo Gang Il ),정찬수 ( Jeong Chan Su ),정철호 ( Jeong Cheol Ho ),제영성 ( Je Yeong Seong ),임창현 ( Im Chang Hyeon 대한내과학회 1993 대한내과학회지 Vol.44 No.5
Since 1938, Diphenylhydantoin (DPH) has remained one of the most widely used anticonvulsants for treatment and prevention of seizures. DPH may induce serious damage to the hematopoietic system. Especially, DPH induced severe aplastic anemia is one of the most severe complication and its incidence is extremely rare. We recently expreienced one case of severe aplastic anemia in 52-year-old woman following administration of DPH. Litreature was reviewed briefly.
Wave energy-assisted fluidic self-assembly of LED chips for display applications
Je Jun Ryu,Seong Hyeon Noh,Selim Yun,Chang Wan Park,Seungje Lee,Young Rag Do,Jae Soo Yoo 한국정보디스플레이학회 2022 Journal of information display Vol.23 No.4
Micro-light-emitting diode (micro-LED) displays have excellent image characteristics, particularly in terms of contrast ratio, response to electric field, and color expressions. However, these are expensive due to the price of the LED chips. This can be overcome by reducing the size of the LED chip, but the efficiency will decrease as a result. Moreover, the rapid and accurate arrangement of a few million chips with a size of ∼50μm to form pixels on the substrate is a challenging task. In this study, fluidic self-assembly process was introduced. The self-assembly design and implementation were limited to building a micro-scale system. With geometric constraints, external forces may influence the outcome of a self-assembled product. In this case, wave energy was used as the external force to manipulate the LED chips on the substrate. Target-generated waveforms in the fluid were used to control the movement of the LED chips. The arrays of the LED chips were arranged on a fine metal mask, i.e. transfer cartridge. The chips were then transferred to a circuit-printed glass plate by face-toface pressing under high temperature and high pressure. It was found that the wave energy-assisted self-assembly is applicable and beneficial to LED module fabrication.
Hyeon-Young Park,Je-Jung Lee,Jee-Bum Lee,Seong-Jin Kim,Seung-Chul Lee,Young Ho Won,Sook Jung Yun 대한피부과학회 2011 Annals of Dermatology Vol.23 No.-
Castleman’s disease (CD) is an uncommon B-cell lymphoproliferative disorder characterized by lymph node hyperplasia with vascular proliferation. Cutaneous involvement in CD is rare. A 65-year-old man presented with a 7-year history of gradually developing multiple reddish to violaceous indurated plaques on the scalp, trunk, and legs. On physical examination, there were palpable enlarged cervical, axillary,and inguinal lymph nodes. Laboratory examination revealed anemia, thrombocytosis, hyperproteinemia, hypoalbuminemia,and polyclonal hypergammaglobulinemia. An inguinal lymph node biopsy and a skin biopsy were performed and the patient was diagnosed with the plasma cell type of CD. Chemotherapy was started and the lesions have responded to treatment. (Ann Dermatol 23(S2) S169∼S174, 2011)
( Hyeon Young Park ),( Je Jung Lee ),( Jee Bum Lee ),( Seong Jin Kim ),( Seung Chul Lee ),( Young Ho Won ),( Sook Jung Yun ) 대한피부과학회 2011 Annals of Dermatology Vol.23 No.2s
Castleman`s disease (CD) is an uncommon B-cell lymphoproliferative disorder characterized by lymph node hyperplasia with vascular proliferation. Cutaneous involvement in CD is rare. A 65-year-old man presented with a 7-year history of gradually developing multiple reddish to violaceous indurated plaques on the scalp, trunk, and legs. On physical examination, there were palpable enlarged cervical, axillary, and inguinal lymph nodes. Laboratory examination revealed anemia, thrombocytosis, hyperproteinemia, hypoalbuminemia, and polyclonal hypergammaglobulinemia. An inguinal lymph node biopsy and a skin biopsy were performed and the patient was diagnosed with the plasma cell type of CD. Chemotherapy was started and the lesions have responded to treatment. (Ann Dermatol 23(S2) S169~S174, 2011)