Dellaripa, Paul F.

Plasma surfactant protein-D, matrix metalloproteinase-7, and osteopontin index distinguishes idiopathic pulmonary fibrosis from other idiopathic interstitial pneumonias

White, E. S., Xia, M., Murray, S., Dyal, R., Flaherty, C. M., Flaherty, K. R., Moore, B. B., Cheng, L., Doyle, T. J., Villalba, J., et al. (2016) · American Journal of Respiratory and Critical Care Medicine

Interstitial Lung Diseases and Idiopathic Pulmonary FibrosisOccupational and environmental lung diseases

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Rituximab in the treatment of interstitial lung disease associated with antisynthetase syndrome: a multicenter retrospective case review

Doyle, T. J., Dhillon, N., Madan, R., Cabral, F., Fletcher, E. A., Koontz, D. C., Aggarwal, R., Osorio, J. C., Rosas, I. O., Oddis, C. V., et al. (2018) · The Journal of Rheumatology

Inflammatory Myopathies and DermatomyositisInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

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Survival and outcomes after lung transplantation for non-scleroderma connective tissue–related interstitial lung disease

Courtwright, A. M., El-Chemaly, S., Dellaripa, P. F., & Goldberg, H. J. (2017) · The Journal of Heart and Lung Transplantation

Transplantation: Methods and OutcomesInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

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Exploration of the genetic architecture of ANCA-associated vasculitis

Byun, J., Shaw, V. R., Zhu, C., Han, Y., Sun, R., Zhang, Z., Xiao, X., Pinder, B. D., Zhang, J., Tadesse, Y., et al. (2026) · eBioMedicine

Vasculitis and related conditionsGenetic Associations and Epidemiology

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