Interstitial pneumonia with autoimmune features show better survival and less exacerbations compared to idiopathic pulmonary fibrosis

BACKGROUND: Patients with interstitial lung disease (ILD) who show features related to autoimmunity without meeting criteria for a defined connective tissue disease are categorized as interstitial pneumonia with autoimmune features (IPAF). The present study compared clinical characteristics and clin...

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Detalles Bibliográficos
Autores principales: Lim, Jeong Uk, Gil, Bo Mi, Kang, Hye Seon, Oh, Jongyeol, Kim, Yong Hyun, Kwon, Soon Seog
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610995/
https://www.ncbi.nlm.nih.gov/pubmed/31272428
http://dx.doi.org/10.1186/s12890-019-0868-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610995/
https://www.ncbi.nlm.nih.gov/pubmed/31272428
http://dx.doi.org/10.1186/s12890-019-0868-9

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