Results 131 to 140 of about 5,412 (184)
Monocyte/Macrophage Subsets in the Peripheral Blood, Their Related Cytokines, and Circulating Markers of Fibrosis in Active Takayasu Arteritis and Longitudinal Changes Following Immunosuppressive Therapy. [PDF]
J Inflamm ResQamar T +9 more
europepmc +1 more source
Frontiers in Pediatrics, 2018 La arteritis de Takayasu es una vasculitis granulomatosa idiopática de la aorta y sus ramas principales. Es más frecuente entre los asiáticos y las mujeres, y constituye una de las vasculitis más comunes en los niños. La inflamación y la proliferación de la íntima conducen al engrosamiento de la pared, lesiones estenóticas u oclusivas y trombosis ...
Ricardo Russo
exaly +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
openaire +4 more sources
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
openaire +4 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources