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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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Библиографические подробности
Опубликовано в: :Infect Drug Resist
Главные авторы: Magee, Lauren C, Louis, Mariam, Khan, Vaneeza, Micalo, Lavender, Chaudary, Nauman
Формат: Artigo
Язык:Inglês
Опубликовано: Dove 2021
Предметы:
Online-ссылка: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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