查询词典 pemphigoid
- 与 pemphigoid 相关的网络例句 [注:此内容来源于网络,仅供参考]
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Methods 10 cases of anti-P_(200) pemphigoid sera were collected. The skin sections from 6 cases of recessive dystrophic epidermolysis bullosa were studied with these sera by indirect immunofluorescence.
方法收集了10例抗P_(200)类天疱疮血清,对6例隐性遗传性营养不良性大疱性表皮松解症皮肤切片进行了间接免疫荧光研究。
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Results All the 10 anti-P_(200) pemphigoid sera could react with basement membrane zoneof 5 cases of recessive dystrophic epidermolysis bullosa, while epidermolysis bullosa acquisita sera were negative in these skins.
结果发现10例抗P_(200)类天疱疮血清均与5例RDEB皮肤基底膜带反应,而获得性大疱表皮松解症血清对这些皮肤为阴性。
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In addition,in a case of recessive dystrophic epidermolysis bullosa, epidermolysis bullosa acquisita sera react with both BMZ and intracytoplasmic deposition of type Ⅶ collagen,while no anti-P_(200) pemphigoid sera showed this reactivi- ty.
另外,在1例RDEB,EBA血清既与BMZ反应又与Ⅶ型胶原沉积部位的胞浆反应,而抗P_(200)类天疱疮血清无此反应。
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The ultrastructural localization of the immunoglobulin and complements in diseased skin of several sub-epidermal bullous diseases, including 1 case of Bullous Pemphigoid , 3 cases of Epidermolysis Bullous Acquisita , 1 case of Bullous System Lupus Erythematosus and 2 cases of Linear IgA Bullous Dermatoses , was detected by postembedding immunogold electronmicroscopic technique.
利用直接免疫金标电镜技术同时检测几种表皮下大疱病:大疱性类天疱疮1例、获得性大疱性表皮松解症3例、大疱性SLE1例、线性IgA大疱性皮肤病2例皮损组织中免疫球蛋白和补体〓,比较它们沉积部位和形态的异同,以探讨该技术在鉴别不同表皮下大疱病中的意义。
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Methods Studying clinical and laboratory data of 271 inpatients with pemphigus and pemphigoid in our department in recent 11 years.
结合 11年来 2 71例天疱疮和类天疱疮住院患者的临床和实验室资料,分析其中 2 8例天疱疮、类天疱疮的死因及相关因素,并与相应的大疱病生存者作对照及统计学处理。
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Bullous pemphigoid is an acquired autoimmune subepidermal blistering disease caused by autoantibodies against bullous pemphigoid antigen 1 (BPAg1, 230kD) and bullous pemphigoid antigen 2 (BPAg2, 180kD).
类天疱疮乃因体內產生对抗BPAg1(BP230)及BPAg2(BP180)的自体免疫抗体所引起的后天性表皮下水疱病变,其好发於老年人族群。
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Objective: In the sera of most bullous pemphigoid patients, there are auto-antibodies to the basement membrane zone, that fixed on lamella lucida of BMZ was found by immune-electronic microscope, suggesting the disease is a autoimmune disease.
目的:大疱性类天疱疮(bullous pemphigoid,BP)多数患者的血清中存在抗基底膜带成分的自身抗体,免疫电镜显示这种抗体结合在基底膜带的透明板,因此本病为一种自身免疫病。
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Dyshidrosiform pemphigoid is an uncommon form of localized pemphigoid presenting with a persistent vesicular eruptions of the palms and soles.
异汗样类天疱疮是一种不常见的局限型类天疱疮,以手掌及脚底出现持续性水泡的形式来表现。
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56 cases of bullous pemphigoid were studied on the clinical characters and immunol-blot patterns.It was found that bullous pemphigoid happened mostly among old people in bullous type;Autoantigen BP230,BP230/180 and BP 230/180 combined with minor antigens involved in acute phase of BP patient;While BP180 involved mainly in the remission of the disease.
对56例江浙沪地区类天疱疮患者的临床特征和不同靶抗原的关系进行了探讨,发现类天疱疮多发于老年人,并以大疱性多见;在BP的急性期抗体结合230kD、230/180kD、合并条带靶抗原较常出现(86.11%);而在疾病的缓解期抗体结合180kD抗原较常出现(65%);180kD靶抗原并非次要抗原。
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"Topical corticosteroid therapy is effective forboth moderate and severe bullous pemphigoid and is superiorto oral corticosteroid therapy for extensive disease," write Pascal Joly, MD, PhD, from the University of Rouen in France, and colleagues."Topical corticosteroids should be considered the standard treatment for patients with extensive bullous pemphigoid."
外用皮质肾上腺类脂醇治疗对於中度及严重大水疱性类天疱疮都很有效,对於广泛性大水疱性类天疱疮,其效果优於口服皮质肾上腺类脂醇,」法国鲁昂大学的Pascal Joly医师,PhD及其同事写道:「应该考虑将外用皮质肾上腺类脂醇作为广泛性大水疱性类天疱疮治疗的黄金标准。
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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。
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