Results 181 to 190 of about 3,553 (227)
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Rheumatic Disease Clinics of North America, 1990
The cause of Takayasu's arteritis is still obscure. However, certain aspects of the disease have been greatly clarified over the past decade. The disease is worldwide in distribution, with no ethnic group being totally free from risk of the condition. The inflammatory and stenotic phases of the disease frequently coexist, and it is important that the ...
S, Hall, R, Buchbinder
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The cause of Takayasu's arteritis is still obscure. However, certain aspects of the disease have been greatly clarified over the past decade. The disease is worldwide in distribution, with no ethnic group being totally free from risk of the condition. The inflammatory and stenotic phases of the disease frequently coexist, and it is important that the ...
S, Hall, R, Buchbinder
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Biomarkers in Takayasu arteritis
International Journal of Cardiology, 2023Takayasu arteritis (TA) is a rare large vasculitis with unknown etiology, which affects the aorta and its primary branches, as well as the pulmonary and coronary arteries. Cellular and humoral immunity, chronic inflammation, and genetic factors are involved into TA pathogenesis.
Dan, Wen +4 more
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Management of Takayasu arteritis
Best Practice & Research Clinical Rheumatology, 2023This review overviews the challenges in the assessment of disease activity, damage, and therapy of Takayasu arteritis (TAK). Recently developed disease activity scores for TAK are more useful for follow-up visits and require validation of cut-offs for active disease. A validated damage score for TAK is lacking.
Durga Prasanna Misra +6 more
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Takayasu's Arteritis and Temporal Arteritis
Annals of Vascular Surgery, 1992The giant cell arteritides, temporal arteritis and Takayasu’s arteritis, are granulomatous vasculitides affecting medium and large-sized arteries. Temporal arteritis is a systemic panarteritis affecting the elderly, with greater than 95% of patients being over 50 years of age, although a few case reports in young adults and adolescents exist.
C D, Procter, L H, Hollier
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Takayasu arteritis — five doctors in the history of Takayasu arteritis
International Journal of Cardiology, 1996Takayasu arteritis is a chronic vasculitis mainly involving the aorta, its main branches, pulmonary and coronary arteries. Recent international survey has made clear different sex ratio, different involvement and different clinical manifestations among countries.
F, Numano, T, Kakuta
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Update on Takayasu's arteritis
La Presse Médicale, 2015Takayasu arteritis (TAK) is a rare, chronic large-vessel vasculitis (LVV) that predominantly affects aorta, its major branches and the pulmonary arteries. Recent advances in the genetics, clinical course, prognosis, disease assessment with biomakers/imaging/new scoring systems and new treatment options in TAK are discussed in this review.
Fatma, Alibaz-Oner, Haner, Direskeneli
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International Journal of Cardiology, 1996
Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years.
Turkoglu, C +7 more
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Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years.
Turkoglu, C +7 more
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Takayasu arteritis in paediatrics
Cardiology in the Young, 2017AbstractTakayasu arteritis is an idiopathic chronic granulomatous panarteritis predominantly affecting the aorta and its main branches. Although idiopathic, genetic contribution to disease susceptibility is being increasingly recognised. Rare in children, Takayasu arteritis is a worldwide disease with significant morbidity and mortality.
Marisa, Di Santo +2 more
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Pregnancy and Takayasu's arteritis
The American Journal of Medicine, 1983Thirteen patients with Takayasu's arteritis had 30 pregnancies between 1970 and 1982. The 11 pregnancies occurring before the disease became clinically evident were uneventful. Eleven patients had 19 pregnancies after manifestation of the disease. Four ended in abortion, four in cesarean section, and 11 in uneventful vaginal delivery at term. There was
V C, Wong, R Y, Wang, T F, Tse
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Treatment of Takayasu's Arteritis
Annals of Internal Medicine, 1986Excerpt To the editor: The prospective analysis by Shelhamer and colleagues (1) of 20 patients seen at the National Institute of Health is a valuable contribution to the study of Takayasu's arterit...
S, Hall, G G, Hunder
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