Diagnostic Values For Club Cell Secretory Protein (CC16) in Serum of Patients of Combined Pulmonary Fibrosis and Emphysema

MUC5B Promoter Polymorphism and Interstitial Lung Abnormalities

(2013) Gary M. Hunninghake et al.   NEW ENGLAND JOURNAL OF MEDICINE

Premature lung aging and cellular senescence in the pathogenesis of idiopathic pulmonary fibrosis and COPD/emphysema

(2013) Marco Chilosi et al.   Translational Research

An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management

(2011) Ganesh Raghu et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Use of Serum Clara Cell 16-kDa (CC16) Levels as a Potential Indicator of Active Pulmonary Fibrosis in Systemic Sclerosis

(2011) MINORU HASEGAWA et al.   JOURNAL OF RHEUMATOLOGY

Changes in Forced Expiratory Volume in 1 Second over Time in COPD

(2011) Jørgen Vestbo et al.   NEW ENGLAND JOURNAL OF MEDICINE

Idiopathic Pulmonary Fibrosis and Emphysema

(2009) Mayra Mejía et al.   CHEST

The Syndrome of Combined Pulmonary Fibrosis and Emphysema

(2009) Vincent Cottin et al.   CHEST

Pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome

(2009) V. Cottin et al.   EUROPEAN RESPIRATORY JOURNAL

Evaluation of serum CC-16 as a biomarker for COPD in the ECLIPSE cohort

(2008) D A Lomas et al.   THORAX