您要查找的是不是：
- 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。
- 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
- brancher glycogen storage disease 糖原贮积症(Ⅳ型)
- debrancher glycogen storage disease 脱支糖原贮积病
- glycogen storage disease type Ⅱ Ⅱ型糖原累积病
- Glycogen storage disease type Ⅰ 1型糖原累积病
- Generalized glycogen storage disease of infants 婴儿泛发性糖原贮积病
- type Ⅰ-Ⅷ glycogen storage disease Ⅰ-Ⅷ型糖原贮积病
- glycogen storage disease type Ⅲ 糖原累积病Ⅲ型
- glycogen storage disease type III 福布斯病, 糖原贮积病Ⅲ型
- glycogen storage disease type IV 安德森病, 糖原贮积病Ⅳ型(遗传性肝糖原贮积病)
- glycogen storage disease(glycogenosis) 糖原积储症
- X-linked hepatic glycogen storage disease X连锁肝糖原累积症
