Functional associations of pleuroparenchymal fibroelastosis and emphysema with hypersensitivity pneumonitis.

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Functional associations of pleuroparenchymal fibroelastosis and emphysema with hypersensitivity pneumonitis.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Functional associations of ple ...... hypersensitivity pneumonitis.

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Functional associations of ple ...... hypersensitivity pneumonitis.

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type

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label

Functional associations of ple ...... hypersensitivity pneumonitis.

@en

Functional associations of ple ...... hypersensitivity pneumonitis.

@nl

prefLabel

Functional associations of ple ...... hypersensitivity pneumonitis.

@en

Functional associations of ple ...... hypersensitivity pneumonitis.

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P1476

Functional associations of ple ...... h hypersensitivity pneumonitis

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P2093

Anand Devaraj

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Angelo de Lauretis

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Anne Laure Brun

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Arlette Odink

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Athol U Wells

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Claudio Macaluso

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Elisabetta Renzoni

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Joseph Jacob

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Maria Kokosi

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P2860

An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias

Idiopathic pleuroparenchymal fibroelastosis: consideration of a clinicopathological entity in a series of Japanese patients.

Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial.

High resolution CT and histological findings in idiopathic pleuroparenchymal fibroelastosis: features and differential diagnosis

Pulmonary disease assessment in cystic fibrosis: comparison of CT scoring systems and value of bronchial and arterial dimension measurements.

Predictors of survival in coexistent hypersensitivity pneumonitis with autoimmune features

Pleuroparenchymal fibroelastosis: a spectrum of histopathological and imaging phenotypes.

Distinct characteristics of pleuroparenchymal fibroelastosis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis.

Pulmonary Apical Cap-What's Old Is New Again.

Automated Quantitative Computed Tomography Versus Visual Computed Tomography Scoring in Idiopathic Pulmonary Fibrosis: Validation Against Pulmonary Function.

P304

95-101

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scholarly article

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10.1016/J.RMED.2018.03.031

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138

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Sujal R Desai

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2018-03-30T00:00:00Z

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29724400

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5948318

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