Idiopathic pulmonary fibrosis (IPF) is the most common fibrosing lung disease and is associated with a very poor prognosis. IPF manifests histopathologically as usual interstitial pneumonia (UIP) and as subpleural and basal predominant reticulation with honeycombing on high-resolution computed tomography (HRCT) of the chest. When a high-confidence radiologic diagnosis of UIP is made on HRCT, surgical biopsy is rarely required.
Case Report: Pulmonary & Respiratory Medicine
Case Report: Pulmonary & Respiratory Medicine
Case Report: Pulmonary & Respiratory Medicine
Case Report: Pulmonary & Respiratory Medicine
Research Article: Pulmonary & Respiratory Medicine
Research Article: Pulmonary & Respiratory Medicine
Review Article: Pulmonary & Respiratory Medicine
Review Article: Pulmonary & Respiratory Medicine
Review Article: Pulmonary & Respiratory Medicine
Review Article: Pulmonary & Respiratory Medicine
Research Article: Pulmonary & Respiratory Medicine
Research Article: Pulmonary & Respiratory Medicine
Keynote: Cancer Science & Therapy
Keynote: Cancer Science & Therapy
Scientific Tracks Abstracts: Cancer Science & Therapy
Scientific Tracks Abstracts: Cancer Science & Therapy
Keynote: Cancer Science & Therapy
Keynote: Cancer Science & Therapy
Posters & Accepted Abstracts: Journal of Hypertension: Open Access
Posters & Accepted Abstracts: Journal of Hypertension: Open Access
Scientific Tracks Abstracts: Journal of Nephrology & Therapeutics
Scientific Tracks Abstracts: Journal of Nephrology & Therapeutics
Pulmonary & Respiratory Medicine received 1690 citations as per Google Scholar report