Managing Fungal Infections in Cystic Fibrosis Patients: Challenges in Clinical Practice

Cystic Fibrosis (CF) is an autosomal recessive disease characterized by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Impairment of the CFTR protein in the respiratory tract results in the formation of thick mucus, development of inflammation, destruction of b...

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Detalles Bibliográficos
Autores principales: Magee, Lauren C, Louis, Mariam, Khan, Vaneeza, Micalo, Lavender, Chaudary, Nauman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998013/
https://www.ncbi.nlm.nih.gov/pubmed/33790585
http://dx.doi.org/10.2147/IDR.S267219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998013/
https://www.ncbi.nlm.nih.gov/pubmed/33790585
http://dx.doi.org/10.2147/IDR.S267219

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