Takayasu arteritis is a well known yet rare form of large vessel vasculitis. This review details
the history, clinical features, differential diagnoses, classification, and immunology of the …

Takayasu arteritis is an idiopathic granulomatous vasculitis of the aorta and its main
branches and it constitutes one of the more common vasculitides in children. Inflammation …

We conducted a single-center retrospective study to compare the characteristics of
Takayasu arteritis (TA) among white, North African, and black patients in a French tertiary …

Takayasu arteritis (TAK) is a relatively rare systemic vasculitis mainly affecting the aorta and
its large branches. While patients with TAK are more frequently observed in A sian countries …

The past year has seen some notable publications in the field of vasculitis epidemiology.
The appearance of reports from several different parts of the world has permitted …

Takayasu arteritis (TAK) is an immune-mediated vasculitis affecting large arteries first
reported in 1908 from Japan. Case reports of familial onset of TAK from Japan and other …

Takayasu's arteritis is a rare, idiopathic, chronic inflammatory disease with cell-mediated
inflammation, involving mainly the aorta and its major branches. It leads to stenosis …

The systemic vasculitides are multisystem disorders characterised by the inflammation of
blood vessels and tissue necrosis. They are often associated with considerable morbidity …

Background Cerebrovascular disease is one of the possible consequences of Takayasu's
arteritis (TA). However, little is known about the prevalence of stroke/transient ischemic …

Takayasu's arteritis is a systemic vasculitis that involves medium-and large-sized arteries.
Renal artery involvement is a potential manifestation of TA that occurs in 60% of the patients …