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- sphingomyelin storage disease 神经磷脂贮积病
- Objective:To analyze the clinical characteristic of pediatric glycogen storage disease. 目的:分析儿童期肝糖原累积病的临床特点。
- Acid maltase deficiency (AMD) is a form of glycogen storage disease, which is an inherited autosomal recessive disease and rarely found in adults. 摘要酸性麦芽糖酵素缺乏症在成人当中是一个罕见的遗传染色体隐性疾病。
- Methods: 42 children who were diagnosed as liver glycogen storage disease during January 1990 January 2006 were retrospectively analyzed. 方法：回顾分析1990年1月－2006年1月收治的42例以肝脏损害为主的肝糖原累积病患儿的临床资料。
- Type I Glycogen Storage Disease accounts for about 25% of all cases of GSD diagnosed in the USA and in Europe and has an estimated incidence of about 1 in 100,000 live births. 第一类型肝糖储藏疾病占有在美国和欧洲被诊断而且有 100,000 的活的出生的大约 1 被估计的影响之方式的 GSD 的大约 25%25 的所有情形。
- While Sandhoff and Tay-Sachs are relatiely rare, one person in 5,000 is affected by a disease that falls into a category of lysosomal storage diseases. 然而山德霍夫氏病和泰伊-萨克斯病还是相对较少的，5000人中只有1人受到这种溶酶体贮积症的影响。
- Biological control is a promising approach to reduce the storage diseases of jujube fruit. 生物防治是控制枣果采后病害的研究新方向。
- His disease was complicated by pneumonia. 他的病因肺炎并发症而变得更严重。
- Debrancher deficiency glycogen storage disease 脱支链缺乏糖原贮积病
- cerebral glycogen storage disease 大脑性糖原贮积病
- hepatic glycogen storage disease 肝糖原贮积病
- hepatorenal glycogen storage disease 肝肾糖原贮积病:即糖原贮积病Ⅵ型
- Brancher deficiency glycogen storage disease 分支酶缺乏性糖原贮积病GSD
- What can we do to prevent the disease spreading? 我们能做什么来防止这种疾病蔓延呢？
- brancher glycogen storage disease 糖原贮积症(Ⅳ型)
- A storage cell in some amorphous memory devices. 某些非晶体存储器中的一个存储单元。
- John put up a real fight to overcome the disease. 约翰为征服疾病，进行了不屈的斗争。
- The poor man has a serious disease of the liver. 这个可怜的人患有严重的肝病。
- He was found in incurable disease. 他被查出得了不治之症。
- Lymph nodes can be infiltrated by polymorphonuclear cells a condition called lymphadenitis or lymph nodes can be infiltrated by macrophages laden with metabolites as in lipid storage diseases. 淋巴结可由多形核细胞浸润，称淋巴腺病，或由充满代谢物的巨噬细胞浸润，像脂贮积病。
