Pseudomonas aeruginosa in cystic fibrosis patients with c.1652G›A (G551D)‐CFTR treated with ivacaftor—Changes in microbiological parameters - Millar - 2018 - Journal of Clinical Pharmacy and Therapeutics - Wiley Online Library
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Transformative therapies for rare CFTR missense alleles - ScienceDirect
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Novel CFTR modulator combinations maximize rescue of G85E and N1303K in rectal organoids
PDF) Ivacaftor in cystic fibrosis adults: Czech experience with six years of follow-up
Novel CFTR modulator combinations maximize rescue of G85E and N1303K in rectal organoids
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Jun; 160(2)
Filas de registro e pós-registro têm redução - cosmetovigilancia - Anvisa
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Novel CFTR modulator combinations maximize rescue of G85E and N1303K in rectal organoids
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Frontiers | Organoid Technology: A Reliable Developmental Biology Tool for Organ-Specific Nanotoxicity Evaluation
Pseudomonas aeruginosa in cystic fibrosis patients with c.1652G›A (G551D)‐CFTR treated with ivacaftor—Changes in microbiological parameters - Millar - 2018 - Journal of Clinical Pharmacy and Therapeutics - Wiley Online Library
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PDF) Ivacaftor in cystic fibrosis adults: Czech experience with six years of follow-up
LSHTM Research Online
Journal of Cystic Fibrosis | Abstracts of the 40th European Cystic Fibrosis Conference | ScienceDirect.com by Elsevier
38th EUROPEAN CYSTIC FIBROSIS CONFERENCE
Burden of Illness and Pharmacoeconomic Evaluation of Lumacaftor/Ivacaftor in Cystic Fibrosis
Pseudomonas aeruginosa in cystic fibrosis patients with c.1652G›A (G551D)‐CFTR treated with ivacaftor—Changes in microbiological parameters - Millar - 2018 - Journal of Clinical Pharmacy and Therapeutics - Wiley Online Library
Drug modulation, new drugs (section 1) – Cystic Fibrosis Medicine
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Arterial blood gases (ABGs). | Download Table
2017 – Cystic Fibrosis Medicine
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