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Flume, Patrick
One or more keywords matched the following items that are connected to
Flume, Patrick
Item Type
Name
Academic Article
An unusual presentation of cystic fibrosis in an adult.
Academic Article
Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome.
Academic Article
The delta F508 mutation in cystic fibrosis and impact on sinus development.
Academic Article
Ivacaftor in subjects with cystic fibrosis who are homozygous for the F508del-CFTR mutation.
Academic Article
Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screen.
Academic Article
Making the diagnosis of cystic fibrosis.
Concept
Cystic Fibrosis Transmembrane Conductance Regulator
Academic Article
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.
Academic Article
Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial.
Academic Article
Current strategies for the long-term assessment, monitoring, and management of cystic fibrosis patients treated with CFTR modulator therapy.
Academic Article
The challenges of maintaining momentum in CF drug development and approval - Commentary.
Academic Article
Pharmacokinetics and safety of cavosonstat (N91115) in healthy and cystic fibrosis adults homozygous for F508DEL-CFTR.
Academic Article
Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor.
Academic Article
Pediatric and Adult Recommendations Vary for Sibling Testing in Cystic Fibrosis.
Academic Article
Cystic Fibrosis: Translating Molecular Mechanisms into Effective Therapies.
Academic Article
The study of CFTR modulators in the very young.
Academic Article
A phase 3 study of tezacaftor in combination with ivacaftor in children aged 6 through 11?years with cystic fibrosis.
Academic Article
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study.
Academic Article
Building global development strategies for cf therapeutics during a transitional cftr modulator era.
Academic Article
Treatment of pulmonary exacerbations in cystic fibrosis.
Academic Article
Disease burden in people with cystic fibrosis heterozygous for F508del and a minimal function mutation.
Academic Article
A case report of CFTR modulator administration via carrier mother to treat meconium ileus in a F508del homozygous fetus.
Academic Article
Telehealth and CFTR modulators: Accelerating innovative models of cystic fibrosis care.
Search Criteria
Cystic Fibrosis Transmembrane Conductance Regulator