Essential cookies keep the library working. With your permission, we'd also like to use analytics to see what's useful and improve the experience. Read our Privacy Policy or Cookie Policy.
Checking your access to this record.
Introduction Wegener’s disease, currently called granulomatosis with polyangiitis, is a systemic necrotizing vasculitis of small vessels. Orthootolaryngology, lung and kidney manifestations dominate the clinical signs, although other organs may also be affected [1]. It is typically associated with nodular opacity type pulmonary lesions of varying size developing towards excavation. Pulmonary fibrosis is
Copy in another style
Ndongo, S., Pouye, A., Azankpan, E., Ndao, A. C., & Diop, T. M. (2014). Pulmonary fibrosis indicative of granulomatosis with polyangiitis initially believed to be sjögren’s syndrome. Internal Medicine Inside, 2(1), 6–6. https://doi.org/10.7243/2052-6954-2-6
Metadata is harvested from open-access indexes and can be incomplete. Check a citation against the published version before relying on it — see our open access & attribution policy.
Alexandre Gallerand, Stoyan Ivanov
In Discovery Immunology
Lucía Toca Pérez, Miriam Alonso Fernández
In Clínica Contemporánea
Eduardo de Santibáñes, Claudio Bassi
In Annals of Surgery
John P. Stein, Stuart D. Boyd
In Journal of Clinical Oncology