Combined Corticosteroid and Cyclophosphamide Therapy Does Not Alter Survival in Idiopathic Pulmonary Fibrosis-Reference-Cited by-同舟云学术

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Combined Corticosteroid and Cyclophosphamide Therapy Does Not Alter Survival in Idiopathic Pulmonary Fibrosis

Published:2004-06 Issue:6 Volume:125 Page:2169-2174
ISSN:0012-3692
Container-title:Chest
language:en
Short-container-title:Chest

Author:

Collard Harold R.,Ryu Jay H.,Douglas William W.,Schwarz Marvin I.,Curran-Everett Douglas,King Talmadge E.,Brown Kevin K.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference34 articles.

1. Idiopathic pulmonary fibrosis: diagnosis and treatment; international consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS);Am J Respir Crit Care Med,2000

2. Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification;Katzenstein;Am J Respir Crit Care Med,1998

3. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis;Bjoraker;Am J Respir Crit Care Med,1998

4. A histologic pattern of nonspecific interstitial pneumonia is associated with a better prognosis than usual interstitial pneumonia in patients with cryptogenic fibrosing alveolitis;Daniil;Am J Respir Crit Care Med,1999

5. The prognostic significance of the histologic pattern of interstitial pneumonia in patients with the clinical entity of cryptogenic fibrosing alveolitis;Nicholson;Am J Respir Crit Care Med,2000

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1. ATP-induced fibrogenic pathway in circulating cells obtained by idiopathic pulmonary fibrotic (IPF) patients is not blocked by nintedanib and pirfenidone;Biomedicine & Pharmacotherapy;2024-07

2. French practical guidelines for the diagnosis and management of idiopathic pulmonary fibrosis – 2021 update. Full-length version;Respiratory Medicine and Research;2023-06

3. Nintedanib alleviates pulmonary fibrosis in vitro and in vivo by inhibiting the FAK/ERK/S100A4 signalling pathway;International Immunopharmacology;2022-12

4. Recommandations pratiques pour le diagnostic et la prise en charge de la fibrose pulmonaire idiopathique – Actualisation 2021. Version intégrale;Revue des Maladies Respiratoires;2022-09

5. Targeting Histone Deacetylases in Idiopathic Pulmonary Fibrosis: A Future Therapeutic Option;Cells;2022-05-12

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