Results 171 to 180 of about 3,553 (227)
A comorbidity of ulcerative colitis, ankylosing spondylitis, Takayasu's arteritis and silent thyroiditis: an extensive case-based review. [PDF]
Ann Med Surg (Lond)Ghabally M +7 more
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Association between premature vascular smooth muscle cells senescence and vascular inflammation in Takayasu's arteritis. [PDF]
Ann Rheum DisFang C +11 more
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Takayasu’s Arteritis with Coronary Ectasia, Sclerosing Cholangitis and Liver Cirrhosis [PDF]
, 2014 Kani, Camellia +2 more
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Early diagnosis and standardized treatment are critical to improve the prognosis of patients with Takayasu's arteritis. [PDF]
Rheumatol Immunol ResTian X, Zeng X.
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Current Opinion in Rheumatology, 2021
Purpose of review The purpose of this review is to summarize the recent advances in Takayasu arteritis (TAK), mainly focusing on pathogenesis, imaging modalities, and management. Recent findings Three novel clusters based on angiographic findings were identified in the Indian cohort
Sinem Nihal, Esatoglu, Gulen, Hatemi
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Purpose of review The purpose of this review is to summarize the recent advances in Takayasu arteritis (TAK), mainly focusing on pathogenesis, imaging modalities, and management. Recent findings Three novel clusters based on angiographic findings were identified in the Indian cohort
Sinem Nihal, Esatoglu, Gulen, Hatemi
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Acta Chirurgica Belgica, 2000
This paper reviews the literature of Takayasu's arteritis (T.A.). The concept of this disease has evolved considerably over the past decades. T.A. was first described by Mikito Takayasu in 1908, and was thought to be restricted to south-east Asia. But due to the increasing reports from all over the world, it is well established that T.A. has world-wide
Q, Désiron, R, Zeaiter
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This paper reviews the literature of Takayasu's arteritis (T.A.). The concept of this disease has evolved considerably over the past decades. T.A. was first described by Mikito Takayasu in 1908, and was thought to be restricted to south-east Asia. But due to the increasing reports from all over the world, it is well established that T.A. has world-wide
Q, Désiron, R, Zeaiter
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Current Treatment Options in Cardiovascular Medicine, 2008
Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Curry L, Koening, Carol A, Langford
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Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Curry L, Koening, Carol A, Langford
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Current Treatment Options in Cardiovascular Medicine, 1999
Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
, Mohan, , Kerr
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Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
, Mohan, , Kerr
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Current Rheumatology Reports, 2002
The frequency of Takayasu's arteritis (TA) has been estimated to be 2.9 cases per 1 million people, with a female preponderance, although female-to-male ratio varies from different geographic areas. A high frequency of haplotype A24-B52-DR2 has been found in Japanese patients, without this association in other populations.
Antonio, Fraga, Francisco, Medina
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The frequency of Takayasu's arteritis (TA) has been estimated to be 2.9 cases per 1 million people, with a female preponderance, although female-to-male ratio varies from different geographic areas. A high frequency of haplotype A24-B52-DR2 has been found in Japanese patients, without this association in other populations.
Antonio, Fraga, Francisco, Medina
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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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