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- Amyloidosis cutis dyschromica is a rare distinct type of primary cutaneous amyloidosis characterized by the presence of widespread hypopigmented as well as hyperpigmented macules. 摘要色素异常性皮肤淀粉样变性症是原发性皮肤淀粉样变性症的一个罕见而独特的亚型,其特徵是在皮肤出现广泛的色素沉著及色素脱失的斑点;
- Familial generalized dyschromic amyloidosis cutis 家族性全身性变色性皮肤淀粉样变性
- Amyloidosis cutis nodularis and atrophicans 结节萎缩性皮肤淀粉样变性
- Familial amyloidosis cutis 家族性皮肤淀粉样变性
- amyloidosis cutis [医] 皮肤淀粉样变性
- Cuti saw you walking in the rain! 这样的铃声一定很酷!
- Amyloidosis can go away if the CD disease is successfully treated. 如果CD病被成功的治疗后,淀粉样变性也会消失。
- Method:Reviewed 4 cases of primary amyloidosis of the bladder in our hospital. 方法:回顾性分析4例原发性膀胱淀粉样变的临床资料。
- Objective To improve the diagnostic rate of local amyloidosis of stomach. 目的提高局限性胃淀粉样变病的诊断率。
- Systemic amyloidosis involving the gastrointestinal tract is not infrequent. 摘要全身性类淀粉病偶尔可侵犯胃肠管道。
- Objective To improve the recognition of the primary systemic amyloidosis. 摘要目的提高对原发性淀粉样变的认识。
- Rhizoma Paridis, Scolopendra, Cutis Bufonis, Herba Euphorbiae Humifusae. 七叶一枝花,蟾蜍皮,蜈蚣,地锦草。
- Glenner GG. Amyloid deposists and amyloidosis [J]. N Engl J Med,1980,302:1283. 李新功;姜辉;张爱民.;膀胱局限性淀粉样变性病一例[J]
- Cross's disease, familial amyloidosis, prevents the liver from breaking down a protein called transthyretin. 克罗斯患有一种其家族特有的淀粉样变性疾病,它使肝脏无法分解一种叫做转体基因的蛋白。
- Conclusion(s): Aplasia cutis congenita is easily ignored when the lesion is small. 当先天性表皮发育不全伤口面积很小时,极易被忽略。
- Intense pulsed light with the specific spectrum penetrate cutis, be transformed to heat. 特定谱段的强脉冲光能穿透表皮,被色素团和血红蛋白有选择地吸收并转化为热能。
- Pathological examination of the medial rectus muscle showed positive Congo red stain compatible with amyloidosis. 病理切片检查显示阳性刚果红染色反应。
- And because Cross's amyloidosis was so slow-acting,she would be in her 70s before symptoms set in. 由于克罗斯的淀粉样变性发展缓慢,疾病发作之前她将是70多岁的人了。
- We report this case and also review the literature, and then we suggest a checklist for aplasia cutis congenita. 我们报告此一病例,并整理文献列出一个清单,用以处理先天性表皮发育不全之作业流程。
- Cross's disease,familial amyloidosis,prevents the liver from breaking down a protein called transthyretin. 克罗斯患有一种其家族特有的淀粉样变性疾病,它使肝脏无法分解一种叫做转体基因的蛋白。