Prognostic significance of autoantibodies for idiopathic pulmonary fibrosis: protocol for a systematic review

INTRODUCTION: Idiopathic pulmonary fibrosis(IPF) is chronic fibrosing interstitial pneumonia of unknown aetiology. IPF is diagnosed based on the exclusion of known causes such as connective tissue diseases(CTDs). However, some patients fail to meet defined CTD criteria regardless of an implication o...

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Detalles Bibliográficos
Autores principales: Kamiya, Hiroyuki, Panlaqui, Ogee Mer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Respiratory Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855166/
https://www.ncbi.nlm.nih.gov/pubmed/29523572
http://dx.doi.org/10.1136/bmjopen-2017-020862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855166/
https://www.ncbi.nlm.nih.gov/pubmed/29523572
http://dx.doi.org/10.1136/bmjopen-2017-020862

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