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Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

http://www.wikidata.org/entity/Q34118274

about

Idiopathic interstitial pneumonias with connective tissue diseases features: A review Interaction of Src and Alpha-V Integrin Regulates Fibroblast Migration and Modulates Lung Fibrosis in A Preclinical Model of Lung Fibrosis Characterisation of patients with interstitial pneumonia with autoimmune features.Predictors of diagnosis and survival in idiopathic pulmonary fibrosis and connective tissue disease-related usual interstitial pneumonia.Clinical characteristics and survival in idiopathic pulmonary fibrosis and connective tissue disease-associated usual interstitial pneumonia.Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function Decline Focal adhesion kinase signaling determines the fate of lung epithelial cells in response to TGF-β.Pharmacogenetics and interstitial lung disease.Lung Manifestations in the Rheumatic Diseases.Estimating the incidence of interstitial lung diseases in the Cree of Eeyou Istchee, northern Québec.Unmet needs in the treatment of idiopathic pulmonary fibrosis-insights from patient chart review in five European countries A Pharmacokinetic Bioequivalence Study Comparing Pirfenidone Tablet and Capsule Dosage Forms in Healthy Adult Volunteers.Design of the PF-ILD trial: a double-blind, randomised, placebo-controlled phase III trial of nintedanib in patients with progressive fibrosing interstitial lung disease.The Value and Application of the Six Minute Walk Test in Idiopathic Pulmonary Fibrosis.Azathioprine response in patients with fibrotic connective tissue disease-associated interstitial lung disease.Systematic phenotyping and correlation of biomarkers with lung function and histology in lung fibrosis.

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P2860

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

http://www.wikidata.org/entity/Q34118274

description

2014 nî lūn-bûn

@nan

2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@ast

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@en

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@nl

type

label

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@ast

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@en

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@nl

prefLabel

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@ast

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@en

Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@nl

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Pulmonary function and survival in idiopathic vs secondary usual interstitial pneumonia.

@en

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Amy L Olson

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David Sprunger

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Gregory P Cosgrove

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Jeffrey J Swigris

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Joshua Solomon

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Kevin K Brown

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Stephen K Frankel

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Tristan J Huie

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P2860

Spirometric reference values from a sample of the general U.S. population

Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy

American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Soci

High-dose acetylcysteine in idiopathic pulmonary fibrosis

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management

Long-term outcomes of scleroderma renal crisis.

The clinical course of patients with idiopathic pulmonary fibrosis.

Standardized single breath normal values for carbon monoxide diffusing capacity.

Autoimmune-featured interstitial lung disease: a distinct entity.

Acute exacerbations of idiopathic pulmonary fibrosis

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10.1378/CHEST.13-2388

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Evans R Fernández Pérez

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2014-09-01T00:00:00Z

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