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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Detalles Bibliográficos
Autores principales: Tang, Shan, Ma, Jiachu, Meng, Huaxing, Guo, Junhong, Cao, Shuyan, Wang, Binquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
6600
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837892/
https://www.ncbi.nlm.nih.gov/pubmed/33546050
http://dx.doi.org/10.1097/MD.0000000000024276

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837892/
https://www.ncbi.nlm.nih.gov/pubmed/33546050
http://dx.doi.org/10.1097/MD.0000000000024276

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