Results 141 to 150 of about 7,975 (186)
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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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Annals of Internal Medicine, 1994
To evaluate prospectively the clinical features, angiographic findings, and response to treatment of patients with Takayasu arteritis.60 patients with Takayasu arteritis were studied at the National Institute of Allergy and Infectious Diseases between 1970 and 1990 and were followed for 6 months to 20 years (median follow-up, 5.3 years).Data on ...
G S, Kerr +6 more
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To evaluate prospectively the clinical features, angiographic findings, and response to treatment of patients with Takayasu arteritis.60 patients with Takayasu arteritis were studied at the National Institute of Allergy and Infectious Diseases between 1970 and 1990 and were followed for 6 months to 20 years (median follow-up, 5.3 years).Data on ...
G S, Kerr +6 more
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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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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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Takayasu arteritis in Colombia
International Journal of Cardiology, 1998Takayasu arteritis has been recognized in Colombia just recently, and so far we do not have any report concerning its presentation here. In this first report, some issues related to the presentation of the disease are indicated and compared with those found in the medical literature. No differences were found in age and sex.
C A, Cañas +11 more
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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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Cardiology in the Young, 2008
AbstractTakayasu’s disease is a rare chronic vasculitis of unknown aetiology. Initial symptoms and signs are non-specific, and a high index of suspicion is needed to make the correct diagnosis. The disease is associated with a high incidence of morbidity, and a significant risk of premature death.
Tann, Oliver R. +2 more
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AbstractTakayasu’s disease is a rare chronic vasculitis of unknown aetiology. Initial symptoms and signs are non-specific, and a high index of suspicion is needed to make the correct diagnosis. The disease is associated with a high incidence of morbidity, and a significant risk of premature death.
Tann, Oliver R. +2 more
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