Results 61 to 70 of about 16,344 (265)

ANCA-associated vasculitis – Should we change the standard of care? [PDF]

, 2015
Collaborative clinical trials over the last 25 years have revolutionised the care of patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. This has led to production of management recommendations and standards of care.
Bligny, Bourgarit, Choi, de Groot, De Groot, Fauci, Faurschou, Finkielman, Flossmann, Ghosh, Guillevin, Han, Harper, Hauer, Hoffman, Jayne, Jennette, Jennette, Koldingsnes, Leavitt, Luqmani, Mahr, Masi, Mooney, Mooney, Mukhtyar, Mukhtyar, Mukhtyar, Mukhtyar, Nataraja, Ntatsaki, Pagnoux, Pradhan, Rahmattulla, Rao, Reinhold-Keller, Sharma, Sorensen, Stone, Stone, Suppiah, Talar-Williams, Walsh, Watts, Watts, Watts   +45 more
core   +1 more source

Diagnostic Implications and Correlates of Plasma Adenosine Deaminase 2 Activity and ADA2 Variants

Arthritis &Rheumatology, Volume 78, Issue 3, Page 734-742, March 2026.
Objective Deficiency of adenosine deaminase 2 (DADA2) is a monogenic autoinflammatory disease manifested as polyarteritis nodosa, stroke, and bone marrow failure. Leveraging an international cohort of 200 DADA2 cases, we aimed to characterize the diagnostic utility of a plasma ADA2 enzyme activity assay and understand the implications of residual ADA2 ...
Jian Yue, Courtney E. LeSon, Casey A. Rimland, Kailey Brodeur, Rachel Weng, Evan E. Hsu, Michael T. Lam, Manpreet Meyer, Seigo Okada, Andrew L. D. Hsu, Musaab A. Alhezam, Megan M. Perron, Olha Halyabar, Fatma Dedeoglu, Peter A. Nigrovic, Akiko Shimamura, R. Grant Rowe, Megan A. Cooper, Tiphanie P. Vogel, Miriah Gillispie‐Taylor, Rosemary Peterson, Clara Lin, Katherine D. Nowicki, Kaylee Dollerschell, Taizo A. Nakano, Roxane Labrosse, Alexis‐Virgil Cochino, Andreea Ioan, Leonardo Oliveira Mendonca, Samar Freschi Barros, Jorge Kalil, Javier Perez‐Rojas, Alicia Diaz‐Kuan, Eric S. Sobel, Taha Moussa, Samuel Shang Ming Lee, Li Wearn Koh, Archana Khan, Sodality Sutnga, Raju Khubchandani, Walaa Shoman, Yasmine El Chazli, Benzeeta Pinto, Chengappa Kavadichanda, Roshini S. Abraham, Xiangwei Sun, Qing Zhou, Gsrsnk Naidu, Aman Sharma, Carl Esperanzate, Daniel L. Kastner, Ivona Aksentijevich, Susan J. Kelly, Michael Hershfield, Teresa K. Tarrant, Pui Y. Lee   +55 more
wiley   +1 more source

Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa

Einstein (São Paulo)
Arthritis has been reported as an acute pattern, generally evanescent with oligoarthritis, mostly affecting knees and ankles in childhood systemic polyarteritis nodosa.
Glaucia Vanessa Novak, Koken Hayashi, Kohei Sampa, Yosuke Okumura, Gabriela Ribeiro Viola Ferreira, Clovis Artur Silva   +5 more
doaj   +1 more source

Incidence of ANCA-associated vasculitis in a UK mixed ethnicity population [PDF]

, 2016
Objectives: We aimed to estimate the incidence of ANCA-associated vasculitis in the UK and how this varied by ethnic group. Methods: We identified incident cases of ANCA-associated vasculitis between March 2007 and June 2013 in the Nottingham–Derby ...
Alfred Mahr, Baillargeon, Fiona A. Pearce, Judge, Mathur, Matthew J. Grainge, Peter C. Lanyon, Reena Shaunak, Richard A. Watts, Richard B. Hubbard, Watts   +10 more
core   +1 more source

Glucagon‐Like Peptide 1 Receptor Agonists, Sodium‐Glucose Cotransporter 2 Inhibitors, and Risk of Autoimmune Rheumatic Diseases

Arthritis &Rheumatology, Volume 78, Issue 3, Page 654-664, March 2026.
Objective Glucagon‐like peptide 1 receptor agonists (GLP‐1RAs) and sodium‐glucose cotransporter 2 inhibitors (SGLT2i) facilitate weight loss and exhibit immunomodulatory effects, but their impact on the risk of developing autoimmune rheumatic diseases (ARDs) is unclear.
Derin Karacabeyli, Diane Lacaille, Na Lu, Hui Xie, J. Antonio Aviña‐Zubieta   +4 more
wiley   +1 more source

Pseudovasculitis and corticosteroid therapy [PDF]

, 2018
Pseudovasculitis, vasculitis-like syndromes, vasculitis look-alikes, or mimics of vasculitis represent a heterogeneous collection of disorders that are capable of simulating vasculitis.
Egger, Jean-François, Khatchatourian, Gregory, Mauget, Denis, Ribi, Camillo, Villard, Jean   +4 more
core  

Autoimmune inflammatory disorders, systemic corticosteroids and pneumocystis pneumonia: A strategy for prevention [PDF]

, 2004
Background Pneumocystis pneumonia (PCP) is an increasing problem amongst patients on immunosuppression with autoimmune inflammatory disorders (AID). The disease presents acutely and its diagnosis requires bronchoalveolar lavage in most cases.
Evin Sowden, Andrew J Carmichael, C Chagas, O Goetz, SE Follansbee, JR Stringer, JA Kovacs, AE Wakefield, CB Beard, J Helweg-Larsen, ES Manoloff, SL Vargas, AE Wakefield, L Casanova-Cardiel, S Safrin, JG Gerrard, F Roblot, R Nuesch, SH Yale, SM Arend, NG Mansharamani, MS Bartlett, W Koldingsnes, B Godeau, P Cregan, M Orholm, DB Hellmann, RT Davey Jr, MM Ward, H Bachelez, TL Lamagni, FP Ognibene, SP Raychaudhuri, AJ Porges, SD Hearing, B Godeau, EW Walton, GS Hoffman, A Kadoya, J Phair, G Nevez, DS Stein, WT Hughes, WT Hughes, H Masur   +44 more
core   +2 more sources

When Fever Defies Diagnosis: Wissler–Fanconi Syndrome as an Atypical Presentation of Adult‐Onset Still's Disease

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Adult‐onset Still's disease should be considered in young adults presenting with fever of unknown origin and inflammatory arthritis, even in the absence of rash or sore throat. Recognition of the Wissler–Fanconi variant and early ferritin testing can prevent diagnostic delay and enable prompt, effective immunosuppressive therapy.
Attaina Najeeb, Kamran Taj, Aqsa Abdul Qader, Salar Sultan, Khadija Waleed, Rahmat Gul Omarzai   +5 more
wiley   +1 more source

Spontaneous kidney rupture in a patient with polyarteritis nodosa

Journal of Research in Medical Sciences, 2006
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-sized arteries. It involves the renal arterioles in approximately 80% of cases, but spontaneous retroperitoneal hemorrhage is a rare complication of ...
Ahmad Mohammadi, Mohammad Reza Gharaati, Mohammad Reza Ebadzadeh   +2 more
doaj  

Cutaneous polyarteritis nodosa: A case report with a brief review of literature

Medical Journal of Dr. D.Y. Patil University, 2013
Polyarteritis nodosa (PAN) is a rare vasculitis with multisystem involvement. The definition, diagnostic criteria and validity of cutaneous polyarteritis nodosa (c-PAN) as a variant of classic PAN limited to skin have continued to remain disputed.
Yugal K Sharma, Kedarnath Dash, Neha Goyal, Neha C Virmani   +3 more
doaj   +1 more source