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- lipoidal histiocytosis [医] 类脂组织细胞增多病, 尼曼氏病
- Lipoid histiocytosis 类脂性组织细胞增生症
- A case of Langerhans cell histiocytosis is reported. 报告1例朗格汉斯细胞组织细胞增生症。
- The article reports two cases of cutaneous malignant histiocytosis. 本文报告2例皮肤型恶性组织细胞增生症。
- Aim: To analyze the factors affecting the fluidizing lipoid. 摘要分析了影响流化磷脂流变特性的因素。
- A clinical study of 7 cases of pulmonary Langerhans cell histiocytosis. 肺郎格罕细胞组织细胞增多症7例临床分析。
- Histiocytosis X always had multiple bone lesions with osteolytic character. 此病常见有多处骨骼同时发生骨质溶解之病变。
- Resected area from thymus and all lipoid tissue in the front mediastinum. 切除范围从全胸腺组织到前纵隔和上纵隔的所有脂肪样软组织。
- Inflammatory histiocytosis associated with disturbance of cholesterol metabolism,occurs chiefly in young children. 通常发生在年轻人身上的一种胆固醇代谢病症。
- Its health care efficacy of blood lipoid adjustment and premature senility prevention has been certified by China's Ministry of Public Health. 它以猕猴桃果仁油为主要原料，经中国国家卫生部认定，果王素具有调节血脂、延缓衰老的保健功能。
- Histiocytosis associated with disturbance of cholesterol metabolism, occurs chiefly in young children. 与胆固醇代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
- Among surface-active lipoidal substances, lysolecithin is probably the best studied with regard to its fusing capabilities. 具有表面活性的脂类物质中，溶血卵磷脂就其融合性来说可能是研究得最为彻底的。
- Objective To study the diagnosis and differential diagnosis of sea-blue histiocytosis(SBH). 目的探讨海蓝组织细胞增生症(SBH)的诊断及鉴别诊断。
- Pulmonary histiocytosis X is an uncommon interstitial lung disease that primarily affects young adults. 摘要肺组织细胞症X是一种罕见的间质性肺病，常影响年轻成人病患。
- Recently, it has been found that ECM1 is associated with lipoid proteinosis （LP）and lichen sclerosus（LS） . 细胞外基质蛋白1基因的功能性缺陷可导致类脂质蛋白沉积症的发生；
- Langerhans cell histiocytosis is diagnosed by histological examination and immunohistochemical study. 藉由病理检查及免疫组织学检查证实为兰格罕氏组织细胞增生症。
- Lipoid basically has fat of phosphatide, candy, cholesterol and cholesterol ester to wait. 类脂主要有磷脂、糖脂、胆固醇及胆固醇酯等。
- Histiocytosis associated with disturbance of cholesterol metabolism， occurs chiefly in young children. 与胆固醇代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
- METHODS The rat fed with hyperlipid diet for 30 days,then the lipoid of liver were messured. 方法采用高脂饲料饲喂大鼠,同时给予受试药物30d,实验结束,取血测定胆固醇、甘油三酯、高密度脂蛋白和低密度脂蛋白;
- A similar disease in humans, Hashimoto-Pritzker disease, is also a Langerhans cell histiocytosis. 人类也有类似的疾病，称为朗格汉斯组织细胞增多病。
