Results 81 to 90 of about 166,248 (313)
Eosinophilic vasculitis: an inhabitual and resistant manifestation of a vasculitis
, 2010 A 55-year-old woman was referred because of diffuse pruritic erythematous lesions and an ischemic process of the third finger of her right hand. She was known to have anaemia secondary to hypermenorrhea.
Jandus, P +10 more
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From Interferon Signature to the Clinical Landscape: Type I Interferonopathies
Arthritis &Rheumatology, EarlyView.Objective TypeI interferonopathies are heterogeneous diseases driven by dysregulated type I interferon (IFN‐I) signaling. Diagnosis is challenging due to clinical/molecular variability and the need for IFN‐I quantification. The aim of this study was to characterize the clinical, immunologic, genetic, molecular profiles of patients with suspected ...
Ismail Yaz +13 more
wiley +1 more source
Arthritis &Rheumatology, EarlyView.Objective Somatic DNMT3A mutations are the most common drivers of clonal hematopoiesis in patients with rheumatoid arthritis (RA) and have been associated with seropositive disease and increased markers of inflammation. These mutations are predominantly hypomorphic or dominant‐negative, reducing DNMT3A function.
Yunbing Shen +10 more
wiley +1 more source
[Systemic ANCA-associated vasculitis--diagnosis and therapy]
, 2008 ANCA-associated vasculitis represents a group of small-vessel vasculitides, including Wegener's granulomatosis, microscopic polyangiitis and the Churg-Strauss-syndrome.
Hess, Christof, Eisenberger, Ute
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Sertraline-Induced Leukocytoclastic Vasculitis with Definite Causal Association: A Case Report
, 2023 Antidepressants like sertraline are frequently used to treat psychiatric diseases like depression, panic disorder, and obsessive-compulsive disorder.
Selçuk, Mahmut, Mahmut Selcuk
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Arthritis &Rheumatology, EarlyView.Objective We evaluated baseline characteristics, treatment patterns, and outcomes in patients with systemic autoimmune rheumatic disease–associated progressive pulmonary fibrosis (SARD‐PPF) and evaluated whether outcomes differed by SARD subtype. Methods The ILD‐PRO Registry is a prospective multicenter US registry of patients with PPF.
Sonali J. Bracken +7 more
wiley +1 more source
Vasculitis after blood pressure monitoring [PDF]
, 2016 Introducción Descripción de aparición equimosis en un brazo asociado inicialmente a la toma de presión arterial, por Vasculitis Leucocitoclástica y propuesta de utilidades alternativas de la toma de presión arterial.
Machancoses, Francisco H. +2 more
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Arthritis &Rheumatology, EarlyView.Objective Although Takayasu arteritis (TAK) is not a prototypical autoantibody‐mediated disease, accumulating evidence suggests that B cells are involved. This study aimed to investigate the pathway of B cell activation and its contributions to TAK pathogenesis. Methods Histologic analysis of paravascular lymph nodes and affected arteries was conducted
Chenglong Fang +10 more
wiley +1 more source
Autoantibodies to neutrophil granule proteins: pathogenic potential in vasculitis?
, 1996 The discovery of circulating autoantibodies to neutrophil granule proteins (ANCA), which are present in a high proportion of patients with vasculitis, has revitalised both clinical and experimental research in this area.
Cambridge, G., Locke, I.C.
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Central nervous system vasculitis
, 2003 Vasculitis is an inflammation of the vessel wall. It may be either primary or secondary. Primary vasculitis includes systemic vasculitis (large, medium, and small-vessel vasculitis) and localized vasculitis (isolated angiitis of the central nervous ...
CAROLEI, ANTONIO, SACCO, SIMONA
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