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Standardized nursing management of enzyme replacement therapy for late-onset Pompe disease
Pompe disease or glycogen storage disease type II is a rare autosomal recessive disorder caused by a deficiency of the lysosomal enzyme a-glucosidase. Although enzyme replacement therapy (ERT) with 2 weekly intervals following was considered an effective treatment for Pompe disease in 2006, few pati...
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| Vydáno v: | Medicine (Baltimore) |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Lippincott Williams & Wilkins
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7837892/ https://ncbi.nlm.nih.gov/pubmed/33546050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000024276 |
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