Results 91 to 100 of about 17,480 (219)
Patient with Takayasu arteritis presented as cardiogenic shock
Takayasu arteritis is a chronic inflammatory disease involving the aorta, its main branches and affects particularly young women. Symptomatic coronary artery disease and cardiogenic shock are rare signs of Takayasu arteritis.
Atiye Cengel +3 more
core +1 more source
Bir ergende Takayasu arteritinin atipik presentasyonu
Takayasu arteriti çocuklarda nadir görülen bir hastalıktır. Klinik bulgular özgün değildir ve tanısal bir laboratuvar test mevcut değildir. Burada, atipik bir klinikle başvuran bir ergende Takayasu arteriti sunulmaktadır.
Karakoç Aydıner, Elif +7 more
core +2 more sources
Case of Takayasu syndrome in clinical practice [PDF]
Aim. Modern data about etiology, pathogenesis, clinical symptom of the Takayasu syndrome are given in the article. Materials and methods. Tomography, sonography has important role in the diagnosis of the nonspecific aortoarteritis.
L. O. Kurilets, V. V. Syvolap
core +1 more source
Os autores fazem uma breve revisão de literatura sobre o uso coad-juvante de stents na arterite de Takayasu e apresentam um relato de caso de uma mulher jovem, 27 anos de idade, com quadro de cefaléia holocraniana acompanhada de náuseas, síncopes e ...
Glauber Tercio de Almeida +4 more
doaj +1 more source
A Rare Cause of Abdominal Pain and Fever of Unknown Origin: Takayasu Arteritis
Fever of unknown origin has three most common etiologic categories in children; infectious diseases, connective tissue diseases, and neoplasms. Takayasu arteritis is a chronic vasculitis involving the large vessels, which generally presents with clinical
Özlem Üzüm +5 more
doaj +1 more source
Ramp-rate limitation experiment using induced current method. Part 2: analysis
This paper describes an analysis of ramp-rate limitation experiments performed by a background magnet only without a power supply for the tested cable.
Takayasu, M, Jeong, Sangkwon
core +1 more source
Antiphospholipid antibody-positive Takayasu arteritis: a case report and literature review
ObjectiveTo investigate the clinical features of antiphospholipid antibody-positive Takayasu arteritis and to enhance the awareness of its diagnosis and treatment.MethodsThe clinical features and imaging data of one patient with antiphospholipid antibody-
Wang Ding-ding +7 more
doaj +3 more sources
Granulomatous Vasculitis: An Unusual Manifestation of Metastatic Crohn’s Disease
Australasian Journal of Dermatology, Volume 67, Issue 5, Page e333-e334, August 2026.
Ethan Wei Min Lee +3 more
wiley +1 more source
Pulmonary hypertension in Takayasu arteritis
Aim: To determine the frequency and define the causes of pulmonary hypertension (PH) in patients with Takayasu arteritis (TA)
ŞENER, YUSUF ZİYA +25 more
core +1 more source
Takayasu arteritis, ocular ischemic syndrome, and neovascular glaucoma—A case report
Takayasu arteritis (TA) is an idiopathic, autoimmune rare inflammatory granulomatous large vessel vasculitis affecting males more than females. Ocular involvement occurs in up to 45% of cases due to ocular hypoperfusion.
Sujit Das +3 more
doaj +1 more source

