Dornase alfa in Cystic Fibrosis: indications, comparative studies and effects on lung clearance index

Cystic fibrosis (CF) is the most common inherited disease in Caucasian populations, affecting around 50,000 patients in Europe and 30,000 in United States. A mutation in CF trans-membrane conductance regulator (CFTR) gene changes a protein (a regulated chloride channel), which is expressed in many t...

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Detalles Bibliográficos
Autores principales: Terlizzi, Vito, Castellani, Chiara, Taccetti, Giovanni, Ferrari, Beatrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351191/
https://www.ncbi.nlm.nih.gov/pubmed/35927765
http://dx.doi.org/10.1186/s13052-022-01331-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351191/
https://www.ncbi.nlm.nih.gov/pubmed/35927765
http://dx.doi.org/10.1186/s13052-022-01331-5

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