Results 101 to 110 of about 12,403 (234)

Prevalence, incidence and healthcare burden of eosinophilic granulomatosis with polyangiitis in the UK

ERJ Open Research
Background Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare but serious disease characterised by the combination of small-to-medium vessel vasculitis, blood and tissue eosinophilia, and asthma and/or sinonasal disease.
Jeremiah Hwee, Lorraine Harper, Qinggong Fu, K. Nirantharakumar, George Mu, R. Jakes   +5 more
semanticscholar   +1 more source

Burden of eosinophilic granulomatosis with polyangiitis in Europe

ERJ Open Research
Background and aims Real-world evidence characterising the burden of eosinophilic granulomatosis with polyangiitis (EGPA) in Europe is limited. The aim of this study was to characterise patients in a large European EGPA cohort. Methods This retrospective,
R. Jakes, Namhee Kwon, L. Huynh, Jeremiah Hwee, L. Baylis, R. Alfonso-Cristancho, S. Du, A. Khanal, M. Duh, B. Terrier   +9 more
semanticscholar   +1 more source

Differences in the frequency of macrophage and t cell markers between focal and crescentic classes of antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis [PDF]

, 2017
Funding/Support This study was supported by Tenovus Scotland/Tayside grant award to DK (Grant # T13/15).Peer reviewedPublisher ...
Bray, Susan E., Fleming, Stewart, Kidder, Dana   +2 more
core   +5 more sources

Eosinophilic Granulomatosis with Polyangiitis (EGPA): A Case Report Presenting with Peripheral Polyneuropathy

Journal of Clinical Rheumatology and Immunology
Background: Eosinophilic granulomatosis with polyangiitis is a rare clinical condition with multiple organ involvement. We report a case of a 64-year-old male patient who presented with symptoms of chronic rhinosinusitis, numbness, and pain in both lower
Phuong Nguyen Thi, Ngoc Nguyen Thi Anh, Hoa Dang Hong   +2 more
doaj   +1 more source

Checks and Balances in Autoimmune Vasculitis [PDF]

, 2016
Age-associated changes in the immune system including alterations in surface protein expression are thought to contribute to an increased susceptibility for autoimmune diseases. The balance between the expression of coinhibitory and costimulatory surface
Abdulahad, Wayel H., Boots, Annemieke M. H., Brouwer, Elisabeth, Cadena, Rebeca Hid, Heeringa, Peter, Hospers, G. A. P., Wind, T. T.   +6 more
core   +3 more sources

Intracerebral hemorrhage after IV tPA for stroke as early symptom of ANCA-associated vasculitis

eNeurologicalSci, 2017
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are rare diseases characterized by a necrotizing small-vessel vasculitis and circulating ANCA that comprise granulomatosis with polyangiitis, microscopic polyangiitis, and ...
Neda Zarghami Esfahani, Daniel M. Anderson, Connie Pieper, Harold P. Adams, Jr.   +3 more
doaj   +1 more source

Orbital inflammatory complications of Crohn’s disease: a rare case series [PDF]

, 2018
Orbital inflammatory disease is a rare ophthalmic manifestation of Crohn’s disease. Inflammation is characteristically non-specific, involving one or multiple structures of the orbit.
Abercrombie, Lorraine, Albanese, Giorgio, Kaye, Philip, Monaghan, Tanya M., Moran, Gordon W., Thomas, James D.   +5 more
core   +3 more sources

Evidence-Based Guideline for the diagnosis and management of eosinophilic granulomatosis with polyangiitis

Nature Reviews Rheumatology, 2023
G. Emmi, A. Bettiol, E. Gelain, I. Bajema, A. Berti, S. Burns, M. Cid, J. C. Cohen Tervaert, V. Cottin, E. Durante, Julia U. Holle, A. Mahr, M. D. Del Pero, C. Marvisi, J. Mills, S. Moiseev, F. Moosig, C. Mukhtyar, T. Neumann, I. Olivotto, C. Salvarani, B. Seeliger, R. Sinico, C. Taillé, B. Terrier, N. Venhoff, G. Bertsias, L. Guillevin, D. Jayne, A. Vaglio   +29 more
semanticscholar   +1 more source

Multiple intracerebral hemorrhages secondary to eosinophilic granulomatosis with polyangiitis: A case report and literature review

Kaohsiung Journal of Medical Sciences
Eosinophilic granulomatosis with polyangiitis (EGPA) is a type of systemic vasculitis that affects multiple systems. The most common neurological complication is peripheral nervous system disease, while central nervous system involvement is less common ...
Guo Li, Xinge Liu, Lin Yang
semanticscholar   +1 more source

Characteristics of articular syndrome in systemic vasculitis [PDF]

, 2017
The purpose of the study – investigation the separate joint lesion in systemic vasculitis, their X-ray sonographic characteristics, the correlation of the articular syndrome severity with extra-articular manifestations of the diseases, as well as ...
Gashynova, K., Khaniukov, O., Syniachenko, O., Taktashov, H., Yehudina, Ye.   +4 more
core