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Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Cochrane database of systematic reviews, 2019-09, Vol.9 (9), p.CD001505-CD001505

2019

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Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

The New England journal of medicine, 2019-11, Vol.381 (19), p.1809-1819

2019

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Nutritional Requirements of Lung Transplant Recipients: Challenges and Considerations

Nutrients, 2018-06, Vol.10 (6), p.790

2018

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Re-opening the pediatric pulmonary function laboratory during the ongoing COVID-19 pandemic

Paediatric respiratory reviews, 2022-06, Vol.42, p.49-52

Lands, Larry C.

2022

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Weaving ethics into our activities

Paediatric respiratory reviews, 2021-09, Vol.39, p.40-40

Lands, Larry C.

2021

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Infection prevention and control in cystic fibrosis: One size fits all?

Paediatric respiratory reviews, 2020-11, Vol.36, p.92-93

Lands, Larry C.

2020

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Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Cochrane database of systematic reviews, 2016-04, Vol.4, p.CD001505-CD001505

2016

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Stimulation of the RIG-I/MAVS Pathway by Polyinosinic:Polycytidylic Acid Upregulates IFN-β in Airway Epithelial Cells with Minimal Costimulation of IL-8

The Journal of immunology (1950), 2015-09, Vol.195 (6), p.2829-2841

2015

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The Phosphodiesterase Inhibitor Ensifentrine Reduces Production of Proinflammatory Mediators in Well Differentiated Bronchial Epithelial Cells by Inhibiting PDE4

The Journal of pharmacology and experimental therapeutics, 2020-12, Vol.375 (3), p.414-429

2020

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Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis

American journal of respiratory and critical care medicine, 2019-04, Vol.199 (8), p.987-995

2019

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Preventative therapies for respiratory Syncytial virus (RSV) in children: Where are we now?

Paediatric respiratory reviews, 2024-03, Vol.49, p.24-27

2024

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Virtual Physical Prehabilitation in Lung Transplant Candidates: A Proof-of-Concept Study

Transplant international, 2024, Vol.37, p.12355-12355

2024

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Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Cochrane database of systematic reviews, 2013-06 (6), p.CD001505-CD001505

2013

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Dyspnea in Children: What is driving it and how to approach it

Paediatric respiratory reviews, 2017-09, Vol.24, p.29-31

Lands, Larry C

2017

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Lung ultrasound in children with primary ciliary dyskinesia or cystic fibrosis

Pediatric pulmonology, 2024-09

2024

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Reduced exercise capacity for muscle mass in adolescents living with obesity

Pediatric pulmonology, 2024-05, Vol.59 (5), p.1227-1235

2024

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Candidate markers associated with the probability of future pulmonary exacerbations in cystic fibrosis patients

PloS one, 2014-02, Vol.9 (2), p.e88567

2014

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Lung ultrasound findings in asymptomatic healthy children with asthma

Pediatric pulmonology, 2022-10, Vol.57 (10), p.2474-2480

2022

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Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial

JAMA : the journal of the American Medical Association, 2010-05, Vol.303 (17), p.1707

2010

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Comparison of oscillometry devices using active mechanical test loads

ERJ open research, 2019-10, Vol.5 (4), p.160

2019

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Effect of Azithromycin on Systemic Markers of Inflammation in Patients With Cystic Fibrosis Uninfected With Pseudomonas aeruginosa

Chest, 2012-11, Vol.142 (5), p.1259-1266

2012

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Methacholine challenge test: Comparison of tidal breathing and dosimeter methods in children

Pediatric pulmonology, 2018-02, Vol.53 (2), p.174-180

2018

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Post-transplant outcomes among cystic fibrosis patients undergoing lung transplantation colonized by Burkholderia: A single center cohort study

The Journal of heart and lung transplantation, 2023-07, Vol.42 (7), p.917-924

2023

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Rhinovirus Load Is High despite Preserved Interferon-β Response in Cystic Fibrosis Bronchial Epithelial Cells

PloS one, 2015-11, Vol.10 (11), p.e0143129-e0143129

2015

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Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis

The European respiratory journal, 2014-03, Vol.43 (3), p.817-823

2014

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Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

Nutritional Requirements of Lung Transplant Recipients: Challenges and Considerations

Re-opening the pediatric pulmonary function laboratory during the ongoing COVID-19 pandemic

Weaving ethics into our activities

Infection prevention and control in cystic fibrosis: One size fits all?

Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Stimulation of the RIG-I/MAVS Pathway by Polyinosinic:Polycytidylic Acid Upregulates IFN-β in Airway Epithelial Cells with Minimal Costimulation of IL-8

The Phosphodiesterase Inhibitor Ensifentrine Reduces Production of Proinflammatory Mediators in Well Differentiated Bronchial Epithelial Cells by Inhibiting PDE4

Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis

Preventative therapies for respiratory Syncytial virus (RSV) in children: Where are we now?

Virtual Physical Prehabilitation in Lung Transplant Candidates: A Proof-of-Concept Study

Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis

Dyspnea in Children: What is driving it and how to approach it

Lung ultrasound in children with primary ciliary dyskinesia or cystic fibrosis

Reduced exercise capacity for muscle mass in adolescents living with obesity

Candidate markers associated with the probability of future pulmonary exacerbations in cystic fibrosis patients

Lung ultrasound findings in asymptomatic healthy children with asthma

Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial

Comparison of oscillometry devices using active mechanical test loads

Effect of Azithromycin on Systemic Markers of Inflammation in Patients With Cystic Fibrosis Uninfected With Pseudomonas aeruginosa

Methacholine challenge test: Comparison of tidal breathing and dosimeter methods in children

Post-transplant outcomes among cystic fibrosis patients undergoing lung transplantation colonized by Burkholderia: A single center cohort study

Rhinovirus Load Is High despite Preserved Interferon-β Response in Cystic Fibrosis Bronchial Epithelial Cells

Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis

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