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Idiopathic Pulmonary Fibrosis
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Research works printed but not linked: 5
- ATS/ERS Statement on idiopathic pulmonary fibrosis: Diagnosis and treatment. Am J Respir Crit Care Med 2000;164:646–664.
- ATS/ERS International multidisciplinary consensus classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2002;165:277–304. · DOI · Paper page
- Coultas DB, Zumwalt RE, Black WC, Sobonya RE. The epidemiology of interstitial lung diseases. Am J Respir Crit Care Med 1994;150:967–972. · DOI · Paper page
- Kawabata H, Nagai S, Hayashi M, Nakamura H, Nagao T, Shigematsu M, Kitaichi M, Izumi T. Significance of lung shrinkage on CXR as a prognostic factor in patients with idiopathic pulmonary fibrosis. Respirology 2003;8:351–358. · DOI
- Lynch JP, Thannickal VJ. Idiopathic pulmonary fibrosis. In: Baughman RP, du Bois R, Lynch JP, Wells AU, Eds. Diffuse Lung Disease. A Practical Approach. London: Arnold; 2004:131–151.
Cited by
Cellular senescence mediates fibrotic pulmonary disease
Schafer, M. J., White, T. A., Iijima, K., Haak, A. J., Ligresti, G., Atkinson, E. J., Oberg, A. L., Birch, J., Salmonowicz, H., Zhu, Y., et al. (2017) · Nature Communications · doi:10.1038/ncomms14532 · Cited by 1,613
Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study
Justice, J. N., Nambiar, A. M., Tchkonia, T., LeBrasseur, N. K., Pascual, R., Hashmi, S. K., Prata, L., Masternak, M. M., Kritchevsky, S. B., Musi, N., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2018.12.052 · Cited by 1,261
Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis
Wollin, L., Wex, E., Pautsch, A., Schnapp, G., Hostettler, K. E., Stowasser, S., & Kolb, M. (2015) · European Respiratory Journal · doi:10.1183/09031936.00174914 · Cited by 1,005
Pulmonary fibrosis: patterns and perpetrators
Noble, P. W., Barkauskas, C. E., & Jiang, D. (2012) · Journal of Clinical Investigation · doi:10.1172/jci60323 · Cited by 595
Idiopathic pulmonary fibrosis: pathogenesis and management
Sgalla, G., Iovene, B., Calvello, M., Ori, M., Varone, F., & Richeldi, L. (2018) · Respiratory Research · doi:10.1186/s12931-018-0730-2 · Cited by 573
Metadata
- Venue
- Clinical Atlas of Interstitial Lung Disease
- Publisher
- Springer London
- Published
- 2007-11-24
- Volume
- 61
- Issue
- 3
- Pages
- 41-45
- OpenAlex
- W982046541
- Cited by
- 499
- References
- 0
- FWCI
- 5.37
- Type
- book chapter
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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- CoChat. (2026). Citation check: Idiopathic Pulmonary Fibrosis. https://app.cochat.ai/papers/10.1007/978-1-84628-326-0_6
- The paper
- Idiopathic Pulmonary Fibrosis. (2007). Clinical Atlas of Interstitial Lung Disease. https://doi.org/10.1007/978-1-84628-326-0_6
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
