A retrospective study on enzyme replacement therapy in patients with Gaucher disease

A retrospective study on enzyme replacement therapy in patients with Gaucher disease

OBJECTIVE: Gaucher disease is the most common lysosomal storage disorder. A deficiency of beta-glucocerebrosidase causes accumulation of the glucocerebroside in macrophages throughout the body. This study summarizes the effects of enzyme replacement therapy (ERT) with Imiglucerase in children with G...

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Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 44(2006), 9 vom: 12. Sept., Seite 653-6
1. Verfasser: Duan, Yan-long (VerfasserIn)
Weitere Verfasser: Zhang, Yong-hong, Zang, Yan, Shi, Hui-ping, Zhang, Wei-min, Hu, Ya-mei
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:Journal Article Recombinant Proteins Glucosylceramidase EC 3.2.1.45 imiglucerase Q6U6J48BWY