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International guidelines for the management ofANCA-associated systemic vasculitides
Современная ревматология, 2019 The paper deals with international guidelines for the management of antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (SVs) that are a group of severe life-threatening immune-mediated diseases. This group includes granulomatosis
T. V. Beketova
doaj +1 more source
Update of Management of ANCA-Associated Vasculitis
Journal of Clinical Rheumatology and Immunology, 2021 Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is associated with significant morbidity and mortality. Management of AAV is divided into induction of remission and maintenance of remission.
Hoi San Tang, Shirley King Yee
doaj +1 more source
Cryoglobulinaemic vasculitis: classification and clinical and therapeutic aspects [PDF]
, 2007 Cryoglobulinaemia may cause cutaneous vasculitis and glomerulonephritis, potentially leading to end stage renal failure. An important proportion of cryoglobulinaemias are secondary to hepatitis C virus infection.
Braun, Gerald S. +4 more
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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 +10 more
core +1 more source
Polish Journal of Pathology, 2019 It is well known that acute alveolar haemorrhage (AAH) is attributed to capillaritis in most cases with microscopic polyangiitis (MPA). In this article, we explore the cause of alveolar haemorrhage in MPA patients. In the present study, we extracted four
Naoto Kuroda +3 more
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Current status of the treatment of microscopic polyangiitis and granulomatosis with polyangiitis in Japan [PDF]
, 2012 This study aimed to describe the epidemiologic characteristics of microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) in Japan.
Kurosawa, Michiko +4 more
core +1 more source
Asbestos and Probable Microscopic Polyangiitis
Canadian Respiratory Journal, 2004 Several inorganic dust lung diseases (pneumoconioses) are associated with autoimmune diseases. Although autoimmune serological abnormalities are common in asbestosis, clinical autoimmune/collagen vascular diseases are not commonly reported.
George S Rashed Philteos +4 more
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An immunogenetic perspective of ANCA-associated vasculitides
Egyptian Rheumatology and Rehabilitation, 2022 Background Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of small vessel vasculitides characterized by necrotizan vasculitis and inflammation.
A. Kocaaga, M. Kocaaga
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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 +45 more
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Medial medullary infarction caused by antineutrophil cytoplasmic antibody-related vasculitis: Case report and review of the literature [PDF]
, 2017 Rationale: Medial medullary infarction accounts for less than 1% of brain infarctions, and medial medullary infarctions is very rarely caused by antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis.Patient concerns: We report the case of a 76-
Ishii Kazuhiro +7 more
core +2 more sources