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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMJ Open |
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| Κύριοι συγγραφείς: | , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMJ Publishing Group
2018
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| Θέματα: | |
| Διαθέσιμο Online: | 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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