Mapping IPF helps identify geographic regions at higher risk for disease development and potential triggers

Autor: María Teresa Pay, Inma Salvador, Amalia Moreno, Pilar Rivera-Ortega, Jordi Sans, Claudia Guevara, Damià Perich, Saioa Eizaguirre Anton, Jacobo Sellares, Maria Molina-Molina, Roger Llatjós, Enric Barbeta, Maria Guadalupe Silveira, Vanesa Vicens-Zygmunt, Jordi Dorca, Patricio Luburich, Jaume Bordas-Martinez, Carla Lara Compte, Karina Portillo, Ana Villar, Guillermo Suarez-Cuartin, Jessica Shull, Alejandro Robles-Perez, Diana Badenes-Bonet, M Josefa Cardona, Eva Balcells, Rosa Jolis, Jordi Esplugas, Diego Castillo, Leonardo Esteban, Lurdes Planas-Cerezales, Oriol Jorba, Rosana Blavia, Antoni Rosell, Laia Garcia-Bellmunt, Miriam Olid, Silvia Barril, Guadalupe Bermudo

Publikováno v: RESPIROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Fundacion Sancho el Sabio Fundazioa (FSS)
Respirology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname

Background and objective The relationship between IPF development and environmental factors has not been completely elucidated. Analysing geographic regions of idiopathic pulmonary fibrosis (IPF) cases could help identify those areas with higher aggr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e591ea78b44964d3e3a07c4fefc43ca2
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