Konu "Takayasu arteritis" için Tıp Fakültesi listeleme

Toplam kayıt 3, listelenen: 1-3

    • Capillaroscopic findings in Turkish Takayasu arteritis patients 

      Akdoğan, Ali; Erden, Abdulsamet; Şentürk, Esra Fırat; Kılıç, Levent; Sarı, Alper; Armağan, Berkan; Karadağ, Ömer; Kiraz, Sedat (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 ...

    • Childhood-onset Takayasu arteritis and immunodeficiency: case-based review 

      Sener, S; Basaran, O; Batu, ED; Atalay, E; Esenboga, S; Cagdas, D; Kuskonmaz, Baris; Bilginer, Y; 0zaltın, f; Oguz, B; Duzova, A; Tezcan, I; Ozen, S (2022-09)
      Abstract Takayasu arteritis (TAK) has been rarely reported in patients with immunodeficiency. In this review, we present two cases with childhood-onset TAK (c-TAK) and primary immunodeficiency while reviewing similar ...

    • Identification of Susceptibility Loci for Takayasu Arteritis Througha Large Multi-Ancestral Genome-Wide Association Study 

      Karadağ, Ömer; Ortiz-Fernández, Lourdes; Saruhan-Direskeneli, Güher; Alibaz-Oner, Fatma; Kaymaz-Tahra, Sema; Coit, Patrick; Kong, Xiufang; Kiprianos, Allan P; Maughan, Robert T; Kaymaz-Tahra, Sema; Coit, P; Kong, X; Kiprianos, AP; Maughan, RT; Aydin, SZ .; Aksu K,; Keser, G; Kamali, S; Cunninghame-Graham, DS,; Vyse, TJ,; Sun, Y,; Chen, H,; Grayson, PC,; Tombetti, E,; Jiang, L,; Sawalha , AH (Am J Hum Genet, 2020-12-11)
      Takayasu arteritis is a rare inflammatory disease of large arteries. We performed a genetic study in Takayasu arteritis comprising 6,670 individuals (1,226 affected individuals) from five different populations. We discovered ...