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Other Guidelines

Impact of Trikafta on mothers and babies during pregnancy and lactation

  • Read more about Impact of Trikafta on mothers and babies during pregnancy and lactation

Adverse events in clinical trials in children with CF

  • Read more about Adverse events in clinical trials in children with CF

The association between the function of the cellular salt channel cystic fibrosis transmembrane conductance regulator and lung function in people with cystic fibrosis

  • Read more about The association between the function of the cellular salt channel cystic fibrosis transmembrane conductance regulator and lung function in people with cystic fibrosis

Predicting effects of mutations on CFTR’s mRNA

  • Read more about Predicting effects of mutations on CFTR’s mRNA

“Il faut continuer à poser des questions” patient reported outcome measures in cystic fibrosis: An anthropological perspective

  • Read more about “Il faut continuer à poser des questions” patient reported outcome measures in cystic fibrosis: An anthropological perspective

The Effect of Oral and Intravenous Antimicrobials on Pulmonary Exacerbation Recovery in Cystic Fibrosis

  • Read more about The Effect of Oral and Intravenous Antimicrobials on Pulmonary Exacerbation Recovery in Cystic Fibrosis

Comparing oral glucose tolerance test and continuous glucose monitoring

  • Read more about Comparing oral glucose tolerance test and continuous glucose monitoring

Is hyperpolarised gas magnetic resonance imaging a valid and reliable tool to detect lung health in cystic fibrosis patients? A COSMIN systematic review.

  • Read more about Is hyperpolarised gas magnetic resonance imaging a valid and reliable tool to detect lung health in cystic fibrosis patients? A COSMIN systematic review.

Early acquisition and conversion of Pseudomonas aeruginosa in Hispanic youth with cystic fibrosis in the United States

  • Read more about Early acquisition and conversion of Pseudomonas aeruginosa in Hispanic youth with cystic fibrosis in the United States

The Proteostatic Network Chaperome is Downregulated in F508del Homozygote Cystic Fibrosis

  • Read more about The Proteostatic Network Chaperome is Downregulated in F508del Homozygote Cystic Fibrosis
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