1.in people with gaucher disease , the body is not able to properly produce this enzyme , and the fat can not be broken down.
在戈谢病患者体内，不能完全合成该酶，从而导致葡萄糖脑苷脂不能被降解。
2.Objective: To discuss the clinical &haematological characteristics of Gaucher disease ( GD ).
目的：探讨戈谢病（GD）的临床及血液学特点。
3.in 1991 , enzyme replacement therapy became available as the first effective treatment for gaucher disease.
在1991年，酶补充治疗成为第一种最有效的疗法。
4.Such deficiencies cause lysosomal storage disorders, such as Gaucher's disease, and replacement of the gene is an effective treatment.
这样的缺陷引起溶酶体堆积病（例如，高歇病），基因置换是一种有效的疗法。
5.enzyme replacement therapy can stop and often reverse the symptoms of gaucher disease , allowing patients to enjoy a better quality of life.
酶替换疗法可以阻止和减缓戈谢病的病症，使病人能够更好地享受高质量的生活。
6.Cerebral juvenile and adult form of Gaucher disease
中枢性青少年成人型
7.1 Case of Chronic Granulocyte Leucocythemia combined Gaucher Cell
慢性粒细胞白血病并发戈谢细胞1例
8.Gaucher's disease and refractory epilepsy
高雪病与难治性癫痫
9.Advance in the genetherapy of Gaucher's disease
戈谢氏病基因治疗的新进展