Results 101 to 110 of about 54,323 (280)

Clinical Characteristics and Evolution of Interstitial Lung Disease in Subtypes of Idiopathic Inflammatory Myositis With Prevalent Lung Manifestation: A Retrospective Analysis

open access: yesACR Open Rheumatology, Volume 8, Issue 2, February 2026.
Objective Interstitial lung disease (ILD) is common in idiopathic inflammatory myositis (IIM), particularly in antisynthetase syndrome (ASyS), antimelanoma differentiation‐associated protein 5 (anti‐MDA5) syndrome, and scleromyositis. ILD can progress despite resolution of extrapulmonary symptoms, termed postmyopathic progressive pulmonary fibrosis ...
Julia Clark   +5 more
wiley   +1 more source

The classification, natural history and radiological/histological appearance of idiopathic pulmonary fibrosis and the other idiopathic interstitial pneumonias

open access: yesEuropean Respiratory Review, 2008
The idiopathic interstitial pneumonias (IIPs) are a heterogeneous group of rare interstitial lung diseases (ILDs) or diffuse parenchymal lung diseases, which, as their name implies, are of unknown aetiology.
G. Raghu, A. G. Nicholson, D. Lynch
doaj  

Systemic Sclerosis with Multiple Pulmonary Manifestations [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Systemic sclerosis (SSc) is a chronic autoimmune multisystem disorder characterized by endothelial dysfunction and fibroblast dysfunction, which results in progressive fibrosis of the skin and internal organs more frequently the lungs and gastro ...
MOHAN RAO KOTNUR   +4 more
doaj   +1 more source

Growth factors in idiopathic pulmonary fibrosis: relative roles [PDF]

open access: yes, 2001
Treatment of idiopathic pulmonary fibrosis patients has evolved very slowly; the fundamental approach of corticosteroids alone or in combination with other immunosuppressive agents has had little impact on long-term survival.
Allen, JT, Spiteri, MA
core   +3 more sources

BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia [PDF]

open access: yesEuropean Respiratory Journal, 2003
Idiopathic pulmonary fibrosis (IPF), which has the histological pattern of usual interstitial pneumonia (UIP), is a progressive interstitial lung disease with a poor prognosis. Idiopathic interstitial pneumonias with a histological pattern of nonspecific interstitial pneumonia (NSIP) have a better prognosis than UIP, and may present with a clinical ...
S, Veeraraghavan   +8 more
openaire   +2 more sources

POS0595 ABATACEPT IN USUAL AND IN NON-SPECIFIC INTERSTITIAL PNEUMONIA ASSOCIATED TO RHEUMATOID ARTHRITIS. NATIONAL MULTICENTER STUDY OF 190 PATIENTS [PDF]

open access: bronze, 2021
Belén Atienza‐Mateo   +9 more
openalex   +1 more source

Impact of Wildfire Smoke on Respiratory Disease Associated Healthcare Utilization in Gang‐Won Province, South Korea, in 2017

open access: yesGeoHealth, Volume 10, Issue 2, February 2026.
Abstract This study aimed to elucidate the association between wildfire smoke exposure and healthcare utilization for respiratory diseases in Samcheok (City), Gangwon Province, South Korea, focusing on a major wildfire that occurred on 6–9 May 2017. The relative risks (RRs) of healthcare utilization for respiratory diseases in a direct‐exposure area ...
Min‐Taek Lee   +8 more
wiley   +1 more source

Interstitial pneumonia with autoimmune features and undifferentiated connective tissue disease: Our interdisciplinary rheumatology-pneumology experience, and review of the literature [PDF]

open access: yes, 2016
Background: Interstitial lung diseases (ILDs) are a heterogeneous group of disorders characterized by inflammation and/or fibrosis of the lungs, varying from idiopathic interstitial pneumonias to secondary variants, including the ILDs associated to ...
Cerri, Stefania   +9 more
core   +1 more source

Pathologic Criteria for the Diagnosis of Usual Interstitial Pneumonia vs Fibrotic Hypersensitivity Pneumonitis in Transbronchial Cryobiopsies [PDF]

open access: bronze, 2023
Andrew Churg   +9 more
openalex   +1 more source

Diagnostic value of BAL lymphocytosis in patients with indeterminate for usual interstitial pneumonia imaging pattern

open access: yesEuropean Respiratory Journal, 2019
The introduction of antifibrotic agents to clinical practice and the need to better define patient populations for future clinical trials highlight the importance of accurate diagnosis.
V. Tzilas   +8 more
semanticscholar   +1 more source

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