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Ivacaftor in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del-CFTR Mutation

Chest, 2012-09, Vol.142 (3), p.718-724

2012

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The Dynamics of Disease Progression in Cystic Fibrosis

PloS one, 2016-06, Vol.11 (6), p.e0156752-e0156752

2016

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Calibration and validation of modeled 5-year survival predictions among people with cystic fibrosis treated with the cystic fibrosis transmembrane conductance regulator modulator ivacaftor using United States registry data

PloS one, 2023-04, Vol.18 (4), p.e0283479-e0283479

2023

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The Clinical Biology of Cystic Fibrosis Transmembrane Regulator Protein: Its Role and Function in Extrapulmonary Disease

Chest, 2019-03, Vol.155 (3), p.605-616

Liou, Theodore G

2019

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Refinement of metabolite detection in cystic fibrosis sputum reveals heme correlates with lung function decline

PloS one, 2019-12, Vol.14 (12), p.e0226578-e0226578

2019

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Impact of low-level fine particulate matter and ozone exposure on absences in K-12 students and economic consequences

Environmental research letters, 2020-11, Vol.15 (11), p.114052

2020

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Hypoxia induces expression of angiotensin‐converting enzyme II in alveolar epithelial cells: Implications for the pathogenesis of acute lung injury in COVID‐19

Physiological reports, 2021-05, Vol.9 (9), p.e14854-n/a

2021

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Sputum biomarkers and the prediction of clinical outcomes in patients with cystic fibrosis

PloS one, 2012-08, Vol.7 (8), p.e42748-e42748

2012

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Design of the REVEAL Registry for US Patients With Pulmonary Arterial Hypertension

Mayo Clinic proceedings, 2008-08, Vol.83 (8), p.923-931

2008

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Predicting weight gain in patients with cystic fibrosis on triple combination modulator

Pediatric pulmonology, 2024-06, Vol.59 (6), p.1724-1730

2024

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Mutations in the C-terminal region of the bacteriophage exclusion protein PglX can selectively inactivate restriction in Salmonella

Journal of bacteriology, 2023-10, Vol.205 (10), p.e0020723-e0020723

2023

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Ephrin Ligands are Upregulated in the Saliva of SARS‐CoV‐2 Infected Patients

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Genetic Discovery, Rigorous Statistics, and Pandemic Influenza

Chest, 2014-06, Vol.145 (6), p.1186-1188

2014

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Toxicity effects of short term diesel exhaust particles exposure to human small airway epithelial cells (SAECs) and human lung carcinoma epithelial cells (A549)

Toxicology letters, 2012-12, Vol.215 (3), p.181-192

2012

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Spotlighting "Neutrophil Elastase Triggers the Release of Macrophage Extracellular Traps": A New Catch in Cystic Fibrosis?

American journal of respiratory cell and molecular biology, 2022-01, Vol.66 (1), p.5-7

2022

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Predicting Survival in Pulmonary Arterial Hypertension: Insights From the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL)

Circulation (New York, N.Y.), 2010-07, Vol.122 (2), p.164-172

2010

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Pulmonary Arterial Hypertension: Baseline Characteristics From the REVEAL Registry

Chest, 2010-02, Vol.137 (2), p.376-387

2010

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Microbial Interactions in the Cystic Fibrosis Airway

Journal of clinical microbiology, 2018-08, Vol.56 (8)

2018

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The Uncertain Role of Corticosteroids in the Treatment of COVID-19

JAMA internal medicine, 2021-01, Vol.181 (1), p.139

2021

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Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial

Diabetes care, 2009-10, Vol.32 (10), p.1783-1788

2009

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The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Plays an Important Role in Fetal Human Colon Cell Migration and Proliferation

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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The Changing Picture of Patients With Pulmonary Arterial Hypertension in the United States: How REVEAL Differs From Historic and Non-US Contemporary Registries

Chest, 2011, Vol.139 (1), p.128-137

2011

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Delay in Recognition of Pulmonary Arterial Hypertension: Factors Identified From the REVEAL Registry

Chest, 2011-07, Vol.140 (1), p.19-26

2011

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Evaluation of a five-year predicted survival model for cystic fibrosis in later time periods

Scientific reports, 2020-04, Vol.10 (1), p.6602-6602, Article 6602

2020

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A comparison of aminoglycoside antibiotic serum concentrations collected by peripheral veins and peripherally inserted central catheters in adults with cystic fibrosis

Pediatric pulmonology, 2024-06, Vol.59 (6), p.1740-1746

2024

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Ivacaftor in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del-CFTR Mutation

The Dynamics of Disease Progression in Cystic Fibrosis

Calibration and validation of modeled 5-year survival predictions among people with cystic fibrosis treated with the cystic fibrosis transmembrane conductance regulator modulator ivacaftor using United States registry data

The Clinical Biology of Cystic Fibrosis Transmembrane Regulator Protein: Its Role and Function in Extrapulmonary Disease

Refinement of metabolite detection in cystic fibrosis sputum reveals heme correlates with lung function decline

Impact of low-level fine particulate matter and ozone exposure on absences in K-12 students and economic consequences

Hypoxia induces expression of angiotensin‐converting enzyme II in alveolar epithelial cells: Implications for the pathogenesis of acute lung injury in COVID‐19

Sputum biomarkers and the prediction of clinical outcomes in patients with cystic fibrosis

Design of the REVEAL Registry for US Patients With Pulmonary Arterial Hypertension

Predicting weight gain in patients with cystic fibrosis on triple combination modulator

Mutations in the C-terminal region of the bacteriophage exclusion protein PglX can selectively inactivate restriction in Salmonella

Ephrin Ligands are Upregulated in the Saliva of SARS‐CoV‐2 Infected Patients

Genetic Discovery, Rigorous Statistics, and Pandemic Influenza

Toxicity effects of short term diesel exhaust particles exposure to human small airway epithelial cells (SAECs) and human lung carcinoma epithelial cells (A549)

Spotlighting "Neutrophil Elastase Triggers the Release of Macrophage Extracellular Traps": A New Catch in Cystic Fibrosis?

Predicting Survival in Pulmonary Arterial Hypertension: Insights From the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL)

Pulmonary Arterial Hypertension: Baseline Characteristics From the REVEAL Registry

Microbial Interactions in the Cystic Fibrosis Airway

The Uncertain Role of Corticosteroids in the Treatment of COVID-19

Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial

The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Plays an Important Role in Fetal Human Colon Cell Migration and Proliferation

The Changing Picture of Patients With Pulmonary Arterial Hypertension in the United States: How REVEAL Differs From Historic and Non-US Contemporary Registries

Delay in Recognition of Pulmonary Arterial Hypertension: Factors Identified From the REVEAL Registry

Evaluation of a five-year predicted survival model for cystic fibrosis in later time periods

A comparison of aminoglycoside antibiotic serum concentrations collected by peripheral veins and peripherally inserted central catheters in adults with cystic fibrosis

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