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1. Using Imaging to Predict, Identify, and Monitor Progression of Interstitial Lung Disease: Consensus Findings From a Modified Delphi Study

2. The MUC5B Genotype and Other Common Variants Are Associated With Computational Imaging Features of Usual Interstitial Pneumonia Pattern Among Patients With Idiopathic Pulmonary Fibrosis

3. Fibrosis Scores Per Quantitative High-resolution Computed Tomography at Baseline and the Change Over One Year Predict Subsequent Progressive Pulmonary Fibrosis at 24 Months

4. How Should Patients With Progressive Pulmonary Fibrosis Be Identified? Consensus Findings From a Modified Delphi Study

6. Somatic Mutations of MUC5B Within Lung Tissue in Idiopathic Pulmonary Fibrosis

9. A Multi-Omic Approach to Understanding the Molecular Landscape of IPF

11. Chronic Hypersensitivity Pneumonitis (CHP), an Interstitial Lung Disease (ILD) with Distinct Molecular Signatures

14. Study Design of a Phase III, Randomized, Placebo-Controlled Trial of Nintedanib in Children and Adolescents with Clinically Significant Fibrosing Interstitial Lung Disease (ILD)

15. Among Individuals At-Risk, Pre-Clinical Pulmonary Fibrosis Occurs Commonly and Is Progressive

16. Circulating Plasma Proteins Differentially Detected in Idiopathic Pulmonary Fibrosis and in Subjects with Pre-Clinical Pulmonary Fibrosis

17. Rationale, Design and Objectives of Two Phase III, Randomised, Placebo-Controlled Studies of GLPG1690, a Novel Autotaxin Inhibitor, in Idiopathic Pulmonary Fibrosis (ISABELA 1 and 2)

19. Resequencing study confirms that host defense and cell senescence gene variants contribute to the risk of idiopathic pulmonary fibrosis

20. An Update on the Global Idiopathic Pulmonary Fibrosis (IPF) Collaborative Network: A Platform for IPF Genetics

21. The Global Idiopathic Pulmonary Fibrosis (IPF) Collaborative Network: A Platform for IPF Genetics

22. Decline in pulmonary physiology during treatment of chronic hepatitis C with long-acting interferons and ribavirin.

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