Cystic Fibrosis

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Information for Experts

Cystic Fibrosis Week

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ATS Educational Products

2013

A5 A HITCHHIKER'S GUIDE TO MECHANOBIOLOGY: HOW MATRIX-CYTOSKELETON INTERACTIONS DRIVE CELL BEHAVIOR
A85 METHODS TO STUDY LUNG INJURY AND REPAIR
A91 THERAPEUTIC STRATEGIES IN IDIOPATHIC PULMONARY FIBROSIS: DEBATES BETWEEN BENCH AND BEDSIDE: A PRO-CON DEBATE
B85 SCIENTIFIC BREAKTHROUGHS OF THE YEAR: MECHANISMS OF TISSUE REPAIR
C8 AUTOPHAGY: FRIEND OR FOE IN LUNG DISEASE?
C83 THE NEW ENGLAND JOURNAL OF MEDICINE AND THE JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION. DISCUSSION ON THE EDGE: REPORTS OF RECENTLY PUBLISHED PULMONARY RESEARCH

 

2012

A11 ADULT CYSTIC FIBROSIS: THE ESSENTIALS
B11 PROBING THE LUNG MICROBIOME IN HEALTH AND DISEASE
C3 NEWLY RECOGNIZED AND EMERGING LUNG DISEASES
PG9 THE CELLULAR FOUNDATION OF PEDIATRIC RESPIRATORY DISEASE
PG21 THE PHYSIOLOGIC BASIS OF PEDIATRIC RESPIRATORY DISEASES

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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)