Latin American Registry of Idiopathic Pulmonary Fibrosis (REFIPI): Clinical Characteristics, Evolution and Treatment

Author:

Caro Fabián,Buendía-Roldán Ivette,Noriega-Aguirre Lorena,Alberti María L.,Amaral Alexandre,Arbo Guillermo,Auteri Santiago,Bermúdez Aníbal,Curbelo Pablo,Verduzco Manuel de Jesús Díaz,De la Fuente Isabel,Enghelmayer Juan I.,Fernández Martin,Florenzano Matías,Guillen Fernando,Kairalla Ronaldo,Liberato Yuri,Matiz Carlos,Mejía Mayra,Moyano Viviana,Pachas Alfredo,Escotorin Silvia V.,Tabaj Gabriela,Tavera Esther,Undurraga Alvaro,Varela Brenda,Velazquez José Luis,Selman Moises

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine

Reference29 articles.

1. An Official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management;Raghu;Am J Respir Crit Care Med,2011

2. Recomendaciones para el diagnóstico y tratamiento de la fibrosis pulmonar idiopática;Moises;Alat,2014

3. Cluster analysis-based clinical phenotypes of idiopathic interstitial pneumonias: associations with acute exacerbation and overall survival;Aoshima;BMC Pulm Med,2021

4. Investigating significant health trends in idiopathic pulmonary fibrosis (INSIGHTS-IPF): rationale, aims and design of a nationwide prospective registry;Behr;BMJ Open Respir Res,2014

5. Rationale for and design of the idiopathic pulmonary fibrosis–PRospective outcomes (IPF-PRO) registry;O’Brien;BMJ Open Respir Res,2016

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