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An evidence-based review of the potential benefits of taliglucerase alfa in the treatment of patients with Gaucher disease
Gaucher disease is an inherited lysosomal storage disorder, characterized by deficient activity of glucocerebrosidase leading to storage of glucocerebroside in tissue macrophages. Type I disease, the most prevalent form, lacks central nervous system involvement but presents primarily with variable d...
保存先:
| 第一著者: | |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Dove Medical Press
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3363131/ https://ncbi.nlm.nih.gov/pubmed/22654679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CE.S20201 |
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