Background Takayasu arteritis (TA) is a rare, systemic, inflammatory vasculitis of
granulomatous nature, and still of unknown etiology. It mainly involves the aorta and its …

Takayasu arteritis (TA) is a chronic nonspecific granulomatous vasculitis affecting aorta and
its main branches, coronary and pulmonary arteries. TA often occurs in young women and …

Takayasu arteritis (TA) is a chronic large vessel vasculitis that affects aorta, its main
branches and pulmonary arteries. The inflammatory process results in stenosis, occlusion …

Assessment of the pattern and extent of arterial involvement and measurement of current
disease activity are essential for the management of Takayasu arteritis (TA). Since there is …

Takayasu arteritis (TA) is a rare nonspecific inflammatory disease of unknown cause,
predominantly affecting the aorta and its main branches, coronary arteries, and pulmonary …

Takayasu disease belongs to the group of autoimmune vasculitis which most often affects
the aorta and its branches. It is rare, and it mainly affects young women. Recent …

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 (TAK) is a rare, chronic large-vessel vasculitis (LVV) that predominantly
affects aorta, its major branches and the pulmonary arteries. Recent advances in the …

Takayasu 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 …

Takayasu's arteritis is an idiopathic, systemic inflammatory disease, typically involving the
aorta and its main branches. Cell-mediated autoimmunity has been strongly implicated in its …