ATS Educational Products
2013
2012
ATS Journal articles on Cystic Fibrosis
Cystic Fibrosis: AJRCCM
Progressive Flow-to-Volume Dysanapsis in Cystic Fibrosis A Predictor for Lung Transplantation?
Vol.186, No. 1 (2012), pp. 82-87
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Sputum Biomarkers of Inflammation and Lung Function Decline in Children with Cystic Fibrosis
Vol. 186, No. 9(2012), pp. 857-865
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Disparities in Access to Lung Transplantation for Patients with Cystic Fibrosis by Socioeconomic Status
Vol. 186, No. 10 (2012), pp. 1008-1013
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The Effect of Aspergillus fumigatus Infection on Vitamin D Receptor Expression in Cystic Fibrosis
Vol. 186, No.10 (2012), pp. 999-1007
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β-Adrenergic Sweat Secretion as a Diagnostic Test for Cystic Fibrosis
Vol. 186, No. 8 (2012), pp. 732-739
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Macrophage Migration Inhibitory Factor Enzymatic Activity, Lung Inflammation, and Cystic Fibrosis
Vol. 186, No. 2 (2012), pp. 162-169
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Cystic Fibrosis Pulmonary Guidelines Chronic Medications for Maintenance of Lung Health
Vol. 187, No. 7 (2013), pp. 680-689
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Cystic Fibrosis: AJRCMB
Cystic Fibrosis Therapy: A Community Ecology Perspective
Vol. 48, No. 2 (2013), pp. 150-156
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Immune Responses in Cystic Fibrosis Are They Intrinsically Defective?
Vol. 46, No. 6 (2012), pp. 715-722
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Low Sphingosine-1–Phosphate Impairs Lung Dendritic Cells in Cystic Fibrosis
Vol. 48, No. 2 (2013), pp. 250-257
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Glandular Gene Expression of Sinus Mucosa in Chronic Rhinosinusitis with and without Cystic Fibrosis
Vol. 45, No. 3 (2011), pp. 525-533
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Case Studies of the Spatial Heterogeneity of DNA Viruses in the Cystic Fibrosis Lung
Vol. 46, No. 2 (2012), pp. 127-131
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H2O2 Stimulates Cystic Fibrosis Transmembrane Conductance Regulator through an Autocrine Prostaglandin Pathway, Using Multidrug-Resistant Protein–4
Vol. 49, No. 4 (2013), pp. 672-679
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Cystic Fibrosis: Annals
Changes in Cystic Fibrosis Airway Microbiota at Pulmonary Exacerbation
Vol. 10, No. 3 (2013), pp. 179-187
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Application of a Microsystem-based Project to Improve the Inpatient Care of Adults with Cystic Fibrosis
Vol. 10, No. 3 (2013), pp. 198-204
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An Official American Thoracic Society Workshop Report: Optimal Lung Function Tests for Monitoring Cystic Fibrosis, Bronchopulmonary Dysplasia, and Recurrent Wheezing in Children Less Than 6 Years of Age
Vol.10, No. 2 (2013), pp. S1-S11
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ATS Statements, Guidelines and Reports
ATS Statements, Guidelines and Reports are printed in the American Journal of Respiratory and Critical Care Medicine. These documents are also available in PDF format. You may download one copy of any ATS document; there is no charge for this service. For examples, please Click Here.
- An Official ATS Workshop Report: Optimal Lung Function Tests for Monitoring Cystic Fibrosis, Bronchopulmonary Dysplasia, and Recurrent Wheezing in Children Less Than 6 Years of Age (2013)
