Inhalation Treatment with Glutathione in Patients with Cystic Fibrosis. A Randomized Clinical Trial

Innate immunity in cystic fibrosis lung disease

(2012) D. Hartl et al.   Journal of Cystic Fibrosis

Contribution by Polymorphonucleate Granulocytes to Elevated Gamma-Glutamyltransferase in Cystic Fibrosis Sputum

(2012) Alessandro Corti et al.   PLoS One

Infection, Inflammation, and Lung Function Decline in Infants with Cystic Fibrosis

(2011) Naveen Pillarisetti et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Long-Term Inhaled Dry Powder Mannitol in Cystic Fibrosis

(2011) Moira L. Aitken et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Oxidative stress and antioxidant therapy in cystic fibrosis

(2011) Francesco Galli et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Accurate Assessment of Adherence

(2011) Tracey Daniels et al.   CHEST

356* Use of patient monitoring systems in clinical trials to generate objective information on patients' drug adherence of inhaled medications

(2011) C. Fuchs et al.   Journal of Cystic Fibrosis

Denufosol Tetrasodium in Patients with Cystic Fibrosis and Normal to Mildly Impaired Lung Function

(2010) Frank J. Accurso et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Novel Method to Process Cystic Fibrosis Sputum for Determination of Oxidative State

(2009) A. Hector et al.   RESPIRATION

Cystic Fibrosis: Evolution from a Fatal Disease of Infancy with a Clear Phenotype to a Chronic Disease of Adulthood with Diverse Manifestations

(2008) Clement L. Ren   CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY

Improvement in clinical markers in CF patients using a reduced glutathione regimen: An uncontrolled, observational study

(2008) Alfredo Visca et al.   Journal of Cystic Fibrosis