All Outputs (2)

An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study (2017)
Journal Article
Maher, T. M., Oballa, E., Simpson, J. K., Porte, J., Habgood, A., Fahy, W. A., Flynn, A., Molyneux, P. L., Braybrooke, R., Divyateja, H., Parfrey, H., Rassl, D., Russell, A.-M., Saini, G., Renzoni, E., Duggan, A.-M., Hubbard, R., Wells, A. U., Lukey, P. T., Marshall, R. P., & Jenkins, R. G. (in press). An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study. Lancet Respiratory Medicine, 5(12), https://doi.org/10.1016/S2213-2600%2817%2930430-7

Background: Idiopathic Pulmonary Fibrosis (IPF) is a progressive, fatal condition with a variable disease trajectory. The aim of this study was to evaluate potential biomarkers that predict outcome for people with IPF.
Method: The PROFILE study is a... Read More about An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study.

Can granulomatosis with polyangiitis be diagnosed earlier in primary care? A case–control study (2017)
Journal Article
Pearce, F. A., Hubbard, R. B., Grainge, M. J., Watts, R. A., Abhishek, A., & Lanyon, P. C. (2018). Can granulomatosis with polyangiitis be diagnosed earlier in primary care? A case–control study. QJM: An International Journal of Medicine, 111(1), 39-45. https://doi.org/10.1093/qjmed/hcx194

© The Author 2017. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. Background: People with granulomatosis with polyangiitis (GPA) commonly described long delays before diagnosis. Aim: To study the... Read More about Can granulomatosis with polyangiitis be diagnosed earlier in primary care? A case–control study.