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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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| Publicado en: | BMJ Open |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BMJ Publishing Group
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5855166/ https://ncbi.nlm.nih.gov/pubmed/29523572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2017-020862 |
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