Results 281 to 290 of about 142,658 (312)
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Interstitial lung disease in infancy

Early Human Development, 2020
There is a wide differential diagnosis of early onset respiratory distress especially in term babies, and interstitial lung disease (chILD) is a rare but important consideration in this context. chILD manifesting immediately after birth is usually related to mutations in surfactant protein genes, or conditions related to the Congenital Acinar Dysplasia
Andrew, Bush   +5 more
openaire   +2 more sources

Interstitial Lung Disease in HIV

Clinics in Chest Medicine, 2013
A spectrum of noninfectious, nonmalignant lymphocytic infiltrative disorders, including nonspecific interstitial pneumonitis and lymphocytic interstitial pneumonitis, was frequently described in HIV-infected adults in the precombination antiretroviral therapy (ART) era.
Sarah R, Doffman, Robert F, Miller
openaire   +2 more sources

An emerging interstitial lung disease

The Lancet Respiratory Medicine, 2016
Respiratory Medicine, Royal Brompton & Harefield NHS Foundation Trust, London, UK (P M George PhD); Interstitial Lung Disease Unit, Royal Brompton & Harefield NHS Foundation Trust, London, UK (F Chua PhD); Department of Radiology, Royal Brompton & Harefield NHS Foundation Trust, London, UK (A Devaraj MD); and Department of Histopathology, Royal ...
Peter M, George   +3 more
openaire   +2 more sources

Inherited interstitial lung disease

Clinics in Chest Medicine, 2004
This article focuses on recent advances in the identification of genes and genetic polymorphisms that have been implicated in the development of human interstitial lung diseases. It focuses on the inherited mendelian diseases in which pulmonary fibrosis is part of the clinical phenotype and the genetics of familial idiopathic pulmonary fibrosis and ...
Christine Kim, Garcia, Ganesh, Raghu
openaire   +2 more sources

Interstitial lung disease in scleroderma

Rheumatic Disease Clinics of North America, 2003
Pulmonary fibrosis occurs most patients who have scleroderma. It progresses to severe restrictive lung disease in about 15% of patients and remains a major cause of death in this disease. Risks for developing pulmonary fibrosis include diffuse cutaneous scleroderma and anti-Scl-70 antibodies, and risks for developing progressive pulmonary fibrosis and ...
openaire   +2 more sources

Interstitial Lung Disease in Children

Pediatric Clinics of North America, 1994
Interstitial lung disease in children is a heterogeneous group of disorders of both known and unknown causes that share a common histologic characteristic (i.e., inflammation of the pulmonary interstitium that may resolve completely, partially, or progress to derangement of alveolar structures with varying degrees of fibrosis). The inflammatory process,
R E, Bokulic, B C, Hilman
openaire   +2 more sources

Eosinophilic interstitial lung disease

Current Opinion in Pulmonary Medicine, 2004
Although rare, the eosinophilic lung diseases are being increasingly identified as distinct clinical entities. These disorders are a heterogeneous group of disorders in which there is an increased number of eosinophils in the airways and/or lung parenchyma.
openaire   +2 more sources

Pathology of interstitial lung disease

Clinics in Chest Medicine, 2004
A large and diverse group of pathologic conditions manifests clinically and radiologically as diffuse parenchymal lung disease. Diffuse interstitial lung diseases (ILDs) encompass mainly inflammatory processes that involve the structural elements of this organ.
openaire   +2 more sources

Suspected Interstitial Lung Disease in COPDGene Study

American Journal of Respiratory and Critical Care Medicine, 2023
Jonathan A Rose   +2 more
exaly  

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