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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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Detalhes bibliográficos
Publicado no:Infect Drug Resist
Main Authors: Magee, Lauren C, Louis, Mariam, Khan, Vaneeza, Micalo, Lavender, Chaudary, Nauman
Formato: Artigo
Idioma:Inglês
Publicado em: Dove 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7998013/
https://ncbi.nlm.nih.gov/pubmed/33790585
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IDR.S267219
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