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Toplam kayıt 81, listelenen: 21-30
Which Definition Should be used to Determine Colchicine Resistance Among Patients with Familial Mediterranean Fever?
(Clin Exp Rheumatol, 2018-11-12)
Objectives: Colchicine is the main therapy for familial Mediterranean fever (FMF); however, 5-10% of patients are colchicine-resistant. There is no standard and validated definition for colchicine resistance. We aimed to ...
Avascular necrosis less frequently found in systemic lupus erythematosus patients with the use of alternate day corticosteroid
(TÜBİTAK, 2020-02-13)
Background/aim: Avascular necrosis (AVN) is the death of bone due to compromise of blood flow. The etiology of AVN is multifactorial; corticosteroid usage is the second most significant factor after trauma, and systemic ...
Adalimumab as Treatment for Venous Thrombosis in Behçet's Syndrome: Comment on the Article by Emmi et al
(Wıley, 2019-03-02)
We read with interest the article by Emmi et al 1 regarding the effect of adalimumab (ADA)–based treatment versus disease‐modifying antirheumatic drug (DMARD) therapy for venous thrombosis in Behçet's syndrome (BS). Their ...
Do ANCA-associated vasculitides and IgG4-related disease really overlap or not?
(Wiley, 2019-09-30)
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and immunoglobulin G4-related disease (IgG4-RD) have some common features. The co-occurrence/concurrence of AAV and IgG4-RD was recently ...
Increased incidence of spondyloarthropathies in patients with Takayasu arteritis: a systematic clinical survey
(Elsevier, 2019-02-06)
Abstract
Objectives: Takayasu arteritis and Spondyloarthritis are two distinct inflammatory diseases that affect the same age periods. Increasing number of reports on co-incident Takayasu arteritis-spondyloarthritis ...
Histopathological subgrouping versus renal risk score for the prediction of end-stage renal disease in ANCA-associated vasculitis
(BMJ, 2020-05-01)
In patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV) and renal involvement, the development of end-stage renal disease (ESRD) remains an undesired issue. To date, reported predictors of renal ...
Two cases of glutaric aciduria type II: how to differentiate from inflammatory myopathies?
(Taylor and Francis, 2018-11-19)
Muscle weakness is a nonspecific finding of myopathy of any etiology that include iatrogenic, toxic, endocrinological, infectious, immunologic, and metabolic disorders. Among the metabolic myopathies glutaric aciduria type ...
Capillaroscopic findings in Turkish Takayasu arteritis patients
(TÜBİTAK, 2019-10-24)
Abstract
Background/aim: Abnormal capillaroscopic findings have been reported in vasculitic syndromes such as Behçet’s disease, Henoch–Schönlein purpura, and Wegener’s granulomatosis. This study was conducted to define ...
Correction to: Proposal for a simple algorithm to differentiate adult-onset Still's disease with other fever of unknown origin causes: a longitudinal prospective study
(Springer, 2019-04-01)
The author regrets that the original version of this article contained error. Figure 1 was shown in the wrong version, thus corrected figure is shown in this article.
Some concerns from Turkey
(BMJ, 2018-11-24)
We read the paper written by Kaneko et al with great interest.1 This study demonstrates the safety and efficacy of tocilizumab in patients with adult-onset Still’s disease (AOSD). This randomised placebo-controlled study ...