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- W2912167395 abstract "Abstract Takayasu arteritis (TA), despite being classified as a large vessel vasculitis, has distinct genetic, pathological and clinical features as compared to giant cell arteritis. It is a rare disease seen more commonly in Asian countries. The challenge lies in assessing the degree of inflammation in a narrowed vessel and immunosuppressive therapy improves inflammatory features but is unable to open up an occluded vessel. It may have a positive effect on retarding further occlusion. Like antineutrophil cytoplasmic antibody‐associated vasculitis, TA needs a collaborative effort to do randomized controlled therapy to provide benefit to patients." @default.
- W2912167395 created "2019-02-21" @default.
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- W2912167395 date "2019-01-01" @default.
- W2912167395 modified "2023-10-16" @default.
- W2912167395 title "Takayasu arteritis: A distinct syndrome of large vessel vasculitis: A view point by late Professor Paul Bacon" @default.
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- W2912167395 doi "https://doi.org/10.1111/1756-185x.13383" @default.
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