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Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis

Respiratory research, 2022-12, Vol.23 (1), p.1-11, Article 330

2022

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Pharmacokinetics of Aztreonam in Healthy Subjects and Patients with Cystic Fibrosis and Evaluation of Dose-Exposure Relationships Using Monte Carlo Simulation

Antimicrobial Agents and Chemotherapy, 2007-09, Vol.51 (9), p.3049-3055

2007

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Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

The Lancet (British edition), 2019-11, Vol.394 (10212), p.1940-1948

2019

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Changes in performance of the Pari eFlow rapid and Pari LC Plus during 6 months use by CF patients

Journal of aerosol medicine and pulmonary drug delivery, 2009-09, Vol.22 (3), p.263

2009

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CFTR Modulators: Does One Dose Fit All?

Journal of personalized medicine, 2021-05, Vol.11 (6), p.458

2021

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ECFS best practice guidelines: the 2018 revision

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.153-178

2018

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Home videos of cystic fibrosis patients using tobramycin inhalation powder: Relation of flow and cough

Pediatric pulmonology, 2019-11, Vol.54 (11), p.1794-1800

2019

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Management of Individual Patient Expectations When Starting with Highly Effective CFTR Modulators

Journal of personalized medicine, 2021-08, Vol.11 (8), p.811

2021

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Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis

Science translational medicine, 2016-06, Vol.8 (344), p.344ra84

2016

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Physiological predictors of cardiorespiratory fitness in children and adolescents with cystic fibrosis without ventilatory limitation

Therapeutic advances in respiratory disease, 2022-01, Vol.16, p.17534666211070143-17534666211070143

2022

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Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation

Journal of personalized medicine, 2021-04, Vol.11 (5), p.350

2021

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Azithromycin maintenance therapy in patients with cystic fibrosis: A dose advice based on a review of pharmacokinetics, efficacy, and side effects

Pediatric pulmonology, 2012-07, Vol.47 (7), p.658-665

2012

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Pharmacokinetic interactions between ivacaftor and cytochrome P450 3A4 inhibitors in people with cystic fibrosis and healthy controls

Journal of cystic fibrosis, 2021-09, Vol.20 (5), p.e72-e76

2021

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Report of the European Respiratory Society/European Cystic Fibrosis Society task force on the care of adults with cystic fibrosis

The European respiratory journal, 2016-02, Vol.47 (2), p.420-428

2016

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Design and in vitro performance testing of multiple air classifier technology in a new disposable inhaler concept (Twincer ®) for high powder doses

European journal of pharmaceutical sciences, 2006-06, Vol.28 (3), p.171-178

2006

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The effect of maintenance azithromycin on radiological features in patients with bronchiectasis - Analysis from the BAT randomized controlled trial

Respiratory medicine, 2022-02, Vol.192, p.106718-106718, Article 106718

2022

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Radiological and long‐term clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with advanced lung disease

Pediatric pulmonology, 2023-08, Vol.58 (8), p.2317-2322

2023

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Forskolin-induced swelling of intestinal organoids correlates with disease severity in adults with cystic fibrosis and homozygous F508del mutations

Journal of cystic fibrosis, 2020-07, Vol.19 (4), p.614-619

2020

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Targeted exhaled breath analysis for detection of Pseudomonas aeruginosa in cystic fibrosis patients

Journal of cystic fibrosis, 2022-01, Vol.21 (1), p.e28-e34

2022

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The optimal approach to nutrition and cystic fibrosis: latest evidence and recommendations

Current opinion in pulmonary medicine, 2017-11, Vol.23 (6), p.556-561

2017

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The influence of exocrine pancreatic function on the exposure and pharmacokinetics of ivacaftor in people with cystic fibrosis

Journal of cystic fibrosis, 2023-05, Vol.22 (3), p.564-569

2023

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Development and outcomes of a patient driven cystic fibrosis quality of care improvement project

Journal of cystic fibrosis, 2023-01, Vol.22 (1), p.172-178

2023

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Body Weight and Body Mass Index in Patients with End-Stage Cystic Fibrosis Stabilize After the Start of Enteral Tube Feeding

Journal of the Academy of Nutrition and Dietetics, 2017-11, Vol.117 (11), p.1808-1815

2017

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The prevalence of vascular and metabolic complications after lung transplant in people with cystic fibrosis in a Dutch cohort

Clinics (São Paulo, Brazil), 2023-01, Vol.78, p.100274-100274, Article 100274

2023

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Pharmacokinetics and safety of tobramycin nebulization with the I‐neb and PARI‐LC Plus in children with cystic fibrosis: A randomized, crossover study

British journal of clinical pharmacology, 2019-09, Vol.85 (9), p.1984-1993

2019

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Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis

Pharmacokinetics of Aztreonam in Healthy Subjects and Patients with Cystic Fibrosis and Evaluation of Dose-Exposure Relationships Using Monte Carlo Simulation

Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

Changes in performance of the Pari eFlow rapid and Pari LC Plus during 6 months use by CF patients

CFTR Modulators: Does One Dose Fit All?

ECFS best practice guidelines: the 2018 revision

Home videos of cystic fibrosis patients using tobramycin inhalation powder: Relation of flow and cough

Management of Individual Patient Expectations When Starting with Highly Effective CFTR Modulators

Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis

Physiological predictors of cardiorespiratory fitness in children and adolescents with cystic fibrosis without ventilatory limitation

Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation

Azithromycin maintenance therapy in patients with cystic fibrosis: A dose advice based on a review of pharmacokinetics, efficacy, and side effects

Pharmacokinetic interactions between ivacaftor and cytochrome P450 3A4 inhibitors in people with cystic fibrosis and healthy controls

Report of the European Respiratory Society/European Cystic Fibrosis Society task force on the care of adults with cystic fibrosis

Design and in vitro performance testing of multiple air classifier technology in a new disposable inhaler concept (Twincer ®) for high powder doses

The effect of maintenance azithromycin on radiological features in patients with bronchiectasis - Analysis from the BAT randomized controlled trial

Radiological and long‐term clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with advanced lung disease

Forskolin-induced swelling of intestinal organoids correlates with disease severity in adults with cystic fibrosis and homozygous F508del mutations

Targeted exhaled breath analysis for detection of Pseudomonas aeruginosa in cystic fibrosis patients

The optimal approach to nutrition and cystic fibrosis: latest evidence and recommendations

The influence of exocrine pancreatic function on the exposure and pharmacokinetics of ivacaftor in people with cystic fibrosis

Development and outcomes of a patient driven cystic fibrosis quality of care improvement project

Body Weight and Body Mass Index in Patients with End-Stage Cystic Fibrosis Stabilize After the Start of Enteral Tube Feeding

The prevalence of vascular and metabolic complications after lung transplant in people with cystic fibrosis in a Dutch cohort

Pharmacokinetics and safety of tobramycin nebulization with the I‐neb and PARI‐LC Plus in children with cystic fibrosis: A randomized, crossover study

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