Showing 1 - 20 results of 88 for search '"idiopathic pulmonary fibrosis"', query time: 0.07s Refine Results
  1. 1

    Molecular genetics of idiopathic pulmonary fibrosis by R. N. Mustafin

    Published 2022-06-01
    Subjects: “…idiopathic pulmonary fibrosis…”
    Get full text
    Article
  2. 2
  3. 3

    Macrophage-Derived Biomarkers of Idiopathic Pulmonary Fibrosis by E. Bargagli, A. Prasse, C. Olivieri, J. Muller-Quernheim, P. Rottoli

    Published 2011-01-01
    “…Idiopathic pulmonary fibrosis (IPF) is a severe, rapidly progressive diffuse lung disease. …”
    Get full text
    Article
  4. 4
  5. 5

    Effect and Safety of Mycophenolate Mofetil in Idiopathic Pulmonary Fibrosis by Argyris Tzouvelekis, Evangelos Bouros, Anastasia Oikonomou, Paschalis Ntolios, George Zacharis, George Kolios, Demosthenes Bouros

    Published 2011-01-01
    “…Background. Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic interstitial lung disease with ineffective treatment. …”
    Get full text
    Article
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11

    Analysis of Microarray-Identified Genes and MicroRNAs Associated with Idiopathic Pulmonary Fibrosis by Lichao Fan, Xiaoting Yu, Ziling Huang, Shaoqiang Zheng, Yongxin Zhou, Hanjing Lv, Yu Zeng, Jin-Fu Xu, Xuyou Zhu, Xianghua Yi

    Published 2017-01-01
    “…The aim of this study was to identify potential microRNAs and genes associated with idiopathic pulmonary fibrosis (IPF) through web-available microarrays. …”
    Get full text
    Article
  12. 12

    Anti-Myxovirus Resistance Protein-1 Immunoglobulin A Autoantibody in Idiopathic Pulmonary Fibrosis by Toru Arai, Masaki Hirose, Yoshimasa Hamano, Tomoko Kagawa, Akihiro Murakami, Hiroshi Kida, Atsushi Kumanogoh, Yoshikazu Inoue

    Published 2022-01-01
    “…We have previously analysed serum autoantibody levels in patients with idiopathic pulmonary fibrosis (IPF), idiopathic nonspecific interstitial pneumonia (iNSIP), and healthy controls and identified the autoantibody against anti-myxovirus resistance protein-1 (MX1) to be a specific autoantibody in iNSIP. …”
    Get full text
    Article
  13. 13

    Idiopathic Clubbing Confined to Lower Limb Digits and Idiopathic Pulmonary Fibrosis: An Unusual Association by Rahul Magazine, Ranjan Shetty, Umesh Goneppanavar, Aswini K. Mohapatra

    Published 2012-01-01
    “…A diagnosis of idiopathic pulmonary fibrosis was made on the basis of clinical, spirometric, and high-resolution computed tomography findings. …”
    Get full text
    Article
  14. 14

    Diagnostic Disparity of Previous and Revised American Thoracic Society Guidelines for Idiopathic Pulmonary Fibrosis by Lee Fidler, Shane Shapera, Shikha Mittoo, Theodore K Marras

    Published 2015-01-01
    “…BACKGROUND: A revised guideline for the diagnosis of idiopathic pulmonary fibrosis (IPF) was formulated by the American Thoracic Society (ATS) in 2011 to improve disease diagnosis and provide a simplified algorithm for clinicians. …”
    Get full text
    Article
  15. 15
  16. 16
  17. 17
  18. 18

    A scoping review of the unmet needs of patients diagnosed with idiopathic pulmonary fibrosis (IPF). by Carita Bramhill, Donna Langan, Helen Mulryan, Jessica Eustace-Cook, Anne-Marie Russell, Anne-Marie Brady

    Published 2024-01-01
    “…<h4>Aims</h4>Patients diagnosed with idiopathic pulmonary fibrosis (IPF) have a high symptom burden and numerous needs that remain largely unaddressed despite advances in available treatment options. …”
    Get full text
    Article
  19. 19

    Does Technetium-99m Diethylenetriaminepentaacetate Clearance Predict the Clinical Course of Idiopathic Pulmonary Fibrosis? by Marco Mura, Gelorma Belmonte, Stefano Fanti, Angela Maria Pacilli, Luca Fasano, Maurizio Zompatori, Mario Schiavina, Mario Fabbri

    Published 2004-01-01
    “…Clearance of inhaled technetium-99m diethylenetriaminepentaacetate (99mTc-DTPA) is a potential indicator of disease activity and progression in idiopathic pulmonary fibrosis (IPF). The objective of the present study was to evaluate the prognostic value of 99mTc-DTPA scans in IPF. …”
    Get full text
    Article
  20. 20

    Different Levels of Autophagy Activity in Mesenchymal Stem Cells Are Involved in the Progression of Idiopathic Pulmonary Fibrosis by Hongxia Tao, Qin Lv, Jing Zhang, Lijuan Chen, Yang Yang, Wei Sun

    Published 2024-01-01
    “…Idiopathic pulmonary fibrosis (IPF) is an age-related lung interstitial disease that occurs predominantly in people over 65 years of age and for which there is a lack of effective therapeutic agents. …”
    Get full text
    Article