Ara
Toplam kayıt 14, listelenen: 11-14
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.
Polyarteritis nodosa: lessons from 25 years of experience
(Clin Exp Rheumatol, 2018-10-30)
Objectives: Polyarteritis nodosa is a necrotising vasculitis of predominantly medium size vessels. The present study aimed to summarise the characteristics of PAN patients, and also analyse the trend of decreasing PAN ...
A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2
(J Rheumatol Publ Co, 2019-05-01)
Objective: Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disorder associated with ADA2 mutations. We aimed to investigate the characteristics and ADA2 enzyme activities of patients ...