Cell Therapy for Idiopathic Pulmonary Fibrosis: Rationale and Progress to Date
Cell Therapy for Idiopathic Pulmonary Fibrosis: Rationale and Progress to Date
About this item
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Publisher
Cham: Springer International Publishing
Journal title
Language
English
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Publication information
Publisher
Cham: Springer International Publishing
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Scope and Contents
Contents
Idiopathic pulmonary fibrosis (IPF) is a devastating disease characterized by progressive lung scarring due to unknown injurious stimuli ultimately leading to respiratory failure. Diagnosis is complex and requires a combination of clinical, laboratory, radiological, and histological investigations, along with exclusion of known causes of lung fibro...
Alternative Titles
Full title
Cell Therapy for Idiopathic Pulmonary Fibrosis: Rationale and Progress to Date
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Record Identifier
TN_cdi_proquest_miscellaneous_2440663082
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2440663082
Other Identifiers
ISSN
1173-8804,1179-190X
E-ISSN
1179-190X
DOI
10.1007/s40259-020-00437-8
