Results 91 to 100 of about 30,079 (265)

Clinical Manifestations and Long‐Term Outcomes of Eosinophilic Granulomatosis With Polyangiitis in North America

ACR Open Rheumatology, 2021
To describe clinical manifestations and outcomes in patients with eosinophilic granulomatosis with polyangiitis (EGPA) in North America.
Irena Doubelt, D. Cuthbertson, S. Carette, Sharon A. Chung, Lindsy J. Forbess, N. Khalidi, C. Koening, C. Langford, Carol A. McAlear, L. Moreland, P. Monach, P. Seo, U. Specks, R. Spiera, J. Springer, A. Sreih, K. Warrington, P. Merkel, C. Pagnoux   +18 more
semanticscholar   +1 more source

Head and Neck Manifestations of Eosinophilic Granulomatosis with Polyangiitis: A Systematic Review. [PDF]

, 2016
OBJECTIVE: To conduct the first and only systematic review of the existing literature on head and neck manifestations of eosinophilic granulomatosis with polyangiitis to guide clinical decision making for the otolaryngologist.
Basnyat, Shristi, Goldfarb, Jared M., Nyquist, Gurston G., Rabinowitz, Mindy R., Rosen, Marc R.   +4 more
core   +1 more source

Clinical presentation and outcome of pediatric ANCA-associated glomerulonephritis [PDF]

, 2016
Background Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a small- and medium-sized vasculitis classically seen in adult patients, with peak onset near the fifth to seventh decade of life.
Andreoli, Sharon P., Kouri, Anne M.
core   +1 more source

Interstitial Lung Disease in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis: A European Multicenter Study

Arthritis &Rheumatology, EarlyView.
Objective Interstitial lung disease (ILD) can occur in association with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV‐ILD) or as an isolated entity with positive ANCA (ANCA‐ILD). However, data on the epidemiology and outcomes of these conditions remain limited.
Aglaia Chalkia, Marusa Kotnik, Timothy J. Sadler, Spyridon Katechis, Rachel Jones, Ajay Kamath, Aladdin J. Mohammad, Sara Monti, Chetan Mukhtyar, Viral Nanda, Ioannis Petrakis, Dimitrios Petras, Ashnish Sinha, Pasupathy Sivasothy, Rona Smith, Kostas Stylianou, Dimitrios Vassilopoulos, Judith Babar, David Jayne   +18 more
wiley   +1 more source

T Cells in Vascular Inflammatory Diseases [PDF]

, 2014
Inflammation of the human vasculature is a manifestation of many different diseases ranging from systemic autoimmune diseases to chronic inflammatory diseases, in which multiple types of immune cells are involved. For both autoimmune diseases and chronic
Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Ait-Oufella, Ait-Oufella, Allez, Almanzar, Ammirati, Appay, Bauer, Beeton, Beeton, Beeton, Bettelli, Brouwer, Brouwer, Brown, Cahalan, Capraru, Caruso, Chandy, Chavele, Cohen Tervaert, Davenport, de Boer, de Boer, de Leeuw, de Menthon, Deng, Ebert, Elhage, Erbel, Erbel, Ettinger, Fazilleau, Fontenot, Free, Frostegard, Gan, Gao, Gao, Gephardt, Geri, Gocke, Gotsman, Groh, Gupta, Hauer, Hoshino, Hoshino, Hu, Huber, Imura, Ivanov, Jennette, Jennette, Jonasson, Jonasson, Jovanovic, Kallenberg, Karnell, Kellner, King, King, Kjellev, Klapa, Koch Hansen, Koenen, Komocsi, Laan, Lamprecht, Lamprecht, Langford, Lee, Liston, Lockwood, Mallat, Mallat, Mangan, Matheu, Mestas, Moosig, Morgan, Muller, Niebuhr, Nogueira, Odobasic, Ogasawara, Ooi, Ordonez, Panettieri, Popa, Roselaar, Ruth, Saadoun, Saito, Saito, Samson, Samson, Sanders, Schmitt, Schmitt, Schonermarck, Seta, Smith, Stegeman, Stegeman, Taleb, Terrier, Tse, Valencia, van Es, van Loosdregt, Vincenti, Wang, Weidner, Whitman, Whitman, Whitman, Wilde, Wulff, Xia, Zhou, Zhou, Zhou, Zielinski   +128 more
core   +2 more sources

Effective Performance of the 2022 American College of Rheumatology/EULAR Classification Criteria for Antineutrophil Cytoplasmic Antibody–Associated Vasculitis in Pediatric Patients: An ARChiVe Study

Arthritis &Rheumatology, EarlyView.
Objective To assess the 2022 American College of Rheumatology (ACR)/EULAR classification criteria for antineutrophil cytoplasmic antibody–associated vasculitis (AAV) in children with chronic small‐to‐medium vessel vasculitis. Methods A cohort of 574 patients, identified by physician's diagnosis (MD‐diagnosis) in A Registry of Childhood Vasculitis, was ...
David A. Cabral, Else S. Bosman, Nick McPhate, Simranpreet K. Mann, Kirandeep K. Toor, Kimberly A. Morishita, Raashid Luqmani, Michael W. Beresford, James Bistolarides, Sarah Campillo, Sirirat Charuvanij, Kathryn Cook, Paul Dancey, Marietta de Guzman, Samundeeswari Deepak, Barbara Eberhard, Melissa Elder, Samuel Gagne, Katie Harrison, Adam Huber, Archana Khan, Susan Kim, Marisa S. Klein‐Gitelman, Tzielan C. Lee, Suzanne C. Li, Neil Martin, Flora McErlane, L. Nandini Moorthy, Alvaro H. Orjuela, Jonathan Park, Phil Riley, Alan M. Rosenberg, Susan Shenoi, Vidya Sivaraman, Sodality Sutnga, Tamara Tanner, Stacey E. Tarvin, Marinka Twilt, Linda Wagner‐Weiner, Rae S. M. Yeung, Kelly L. Brown, for the ARChiVe Investigators Network within the PedVas Initiative   +41 more
wiley   +1 more source

The Role of Environmental Factors in the Pathogenesis of Anti-Neutrophil Antibody Associated Vasculitis

, 2014
This review seeks to critically examine the environmental factors reported to be associated with anti-neutrophil antibody associated systemic vasculitis. The published literature was searched in a systematic fashion.
Gatenby, Paul A
core   +1 more source

Is serum HMGB1 a biomarker in ANCA-associated vasculitis? [PDF]

, 2013
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are systemic inflammatory disorders that include granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), Churg-Strauss syndrome and renal limited ...
Bijl, Marc, Bijzet, Johan, Kallenberg, Cees G. M., Limburg, Pieter C., Souza, Alexandre Wagner Silva de, Stegeman, Coen A., Westra, Johanna   +6 more
core   +3 more sources

Intraosseous sarcoidosis imitating peri‐implantitis: A case study

Clinical Advances in Periodontics, EarlyView.
Abstract Background Sarcoidosis is a multisystem granulomatous disorder of unknown cause, typically affecting the lungs and lymph nodes, but it can also involve the eyes, skin, heart, bones, and other organs. The exact cause is unclear, but genetic factors and environmental triggers like infections, chemicals, or dust may play a role.
Magdalena Orlowska, David S. Gottlieb, Kenneth S. Kornman   +2 more
wiley   +1 more source

Update on eosinophilic granulomatosis with polyangiitis.

Allergology International, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) (formerly Churg-Strauss syndrome) is a rare form of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis characterized by eosinophil-rich granulomatous inflammation and small to medium-size ...
S. Furuta, T. Iwamoto, H. Nakajima
semanticscholar   +1 more source