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Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

The Lancet (British edition), 2008-08, Vol.372 (9640), p.719-727

2008

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Comparison of activity and fatigue of the respiratory muscles and pulmonary characteristics between post-polio patients and controls: A pilot study

PloS one, 2017-07, Vol.12 (7), p.e0182036-e0182036

2017

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Long-Term Pulmonary Damage in Surviving Antitoxin-Treated Mice following a Lethal Ricin Intoxication

Toxins, 2024-02, Vol.16 (2), p.103

2024

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CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia

PloS one, 2013-08, Vol.8 (8), p.e72299-e72299

2013

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Differences in Disease Expression Between Primary Ciliary Dyskinesia and Cystic Fibrosis With and Without Pancreatic Insufficiency

Chest, 2014-04, Vol.145 (4), p.738-744

2014

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Pleural line slope in point of care ultrasound assessment of paediatric wheeze may reflect respiratory effort

Acta Paediatrica, 2024-04, Vol.113 (4), p.795-801

2024

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Aspergillus Bronchitis in Cystic Fibrosis

Chest, 2006-07, Vol.130 (1), p.222-226

2006

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Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis

Respiratory medicine, 2017-05, Vol.126, p.39-45

2017

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LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects

PloS one, 2013-03, Vol.8 (3), p.e59436-e59436

2013

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NKp46 regulates allergic responses

European journal of immunology, 2013-11, Vol.43 (11), p.3006-3016

2013

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Control of phospholipase A2 activities for the treatment of inflammatory conditions

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2006-11, Vol.1761 (11), p.1373-1382

2006

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Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform

Frontiers in pediatrics, 2023-12, Vol.11, p.1300968-1300968

2023

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Managing Cystic Fibrosis: Strategies That Increase Life Expectancy and Improve Quality of Life

American journal of respiratory and critical care medicine, 2011-06, Vol.183 (11), p.1463-1471

2011

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Hepatopulmonary Syndrome in Patients With Cystic Fibrosis and Liver Disease

Chest, 2016-02, Vol.149 (2), p.e35-e38

2016

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Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

World journal of gastroenterology : WJG, 2015-01, Vol.21 (1), p.318-325

2015

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Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia

ERJ open research, 2020-10, Vol.6 (4), p.213

2020

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Differences in the Pattern of Structural Abnormalities on CT Scan in Patients With Cystic Fibrosis and Pancreatic Sufficiency or Insufficiency

Chest, 2013-07, Vol.144 (1), p.208-214

2013

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Exercise Challenge Test in 3- to 6-Year-Old Asthmatic Children

Chest, 2007-08, Vol.132 (2), p.497-503

2007

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Continuous intravenous β-lactam antibiotics in cystic fibrosis patients with severe drug hypersensitivity

Annals of allergy, asthma, & immunology, 2014-08, Vol.113 (2), p.229-230

2014

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Systemic Steroid Treatment for Severe Expanding Pneumococcal Pneumonia

Case reports in pediatrics, 2015-01, Vol.2015, p.186302-3

2015

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Anti-inflammatory effects of an inflammatory chemokine: CCL2 inhibits lymphocyte homing by modulation of CCL21-triggered integrin-mediated adhesions

Blood, 2008-12, Vol.112 (13), p.5016-5025

2008

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The Prevalence of Gastroesophageal Reflux in Children With Tracheomalacia and Laryngomalacia

Chest, 2001-02, Vol.119 (2), p.409-413

2001

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Primary ciliary dyskinesia: prospects for new therapies, building on the experience in cystic fibrosis

Paediatric respiratory reviews, 2009-06, Vol.10 (2), p.58-62

2009

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Ethical Dilemma: Elexacaftor-Tezacaftor-Ivacaftor or Lung Transplantation in Cystic Fibrosis and End-Stage Lung Disease?

Chest, 2022-03, Vol.161 (3), p.773-780

2022

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Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

Comparison of activity and fatigue of the respiratory muscles and pulmonary characteristics between post-polio patients and controls: A pilot study

Preconditioning allows engraftment of mouse and human embryonic lung cells, enabling lung repair in mice

Long-Term Pulmonary Damage in Surviving Antitoxin-Treated Mice following a Lethal Ricin Intoxication

CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia

Differences in Disease Expression Between Primary Ciliary Dyskinesia and Cystic Fibrosis With and Without Pancreatic Insufficiency

Pleural line slope in point of care ultrasound assessment of paediatric wheeze may reflect respiratory effort

Aspergillus Bronchitis in Cystic Fibrosis

Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis

LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects

NKp46 regulates allergic responses

Control of phospholipase A2 activities for the treatment of inflammatory conditions

Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform

Managing Cystic Fibrosis: Strategies That Increase Life Expectancy and Improve Quality of Life

Hepatopulmonary Syndrome in Patients With Cystic Fibrosis and Liver Disease

Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia

Differences in the Pattern of Structural Abnormalities on CT Scan in Patients With Cystic Fibrosis and Pancreatic Sufficiency or Insufficiency

Exercise Challenge Test in 3- to 6-Year-Old Asthmatic Children

Continuous intravenous β-lactam antibiotics in cystic fibrosis patients with severe drug hypersensitivity

Systemic Steroid Treatment for Severe Expanding Pneumococcal Pneumonia

Anti-inflammatory effects of an inflammatory chemokine: CCL2 inhibits lymphocyte homing by modulation of CCL21-triggered integrin-mediated adhesions

The Prevalence of Gastroesophageal Reflux in Children With Tracheomalacia and Laryngomalacia

Primary ciliary dyskinesia: prospects for new therapies, building on the experience in cystic fibrosis

Ethical Dilemma: Elexacaftor-Tezacaftor-Ivacaftor or Lung Transplantation in Cystic Fibrosis and End-Stage Lung Disease?

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