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1 y ) was performed (diagnostic standard [ TAB temporal artery biopsy ]).
2 nts suspected of having GCA should undergo a temporal artery biopsy.
3 Vascular tissue was obtained at the time of temporal artery biopsy.
4 erpes zoster antigen was detected on several temporal artery biopsies.
5 l in predicting the likelihood of a positive temporal artery biopsy among patients with a clinical su
6 genesis of the disease but have not replaced temporal artery biopsy as the gold standard for securing
12 iopsy-positive GCA underwent two consecutive temporal artery biopsies, one prior to therapy and one w
13 cent of the control samples were obtained by temporal artery biopsy performed within 1 year of the bi
14 rd to age, frequency of positive findings on temporal artery biopsy (placebo 87%, MTX 79%), or comorb
17 by angiography and 74 control patients with temporal artery biopsy-proven GCA without large vessel i
20 owed a significant association of VZV DNA to temporal artery biopsy samples positive for GCA compared
27 giant cell arteritis -negative results ( TAB temporal artery biopsy subcohort and total study cohort,
29 ers, with good interobserver agreement ( TAB temporal artery biopsy subcohort, kappa = 0.718; total s
31 comparison with the diagnostic standard TAB temporal artery biopsy ( TAB temporal artery biopsy subc
36 ella-zoster virus antigen) was detectable in temporal artery biopsies taken from individuals with gia
37 ts (98 of 185), temporal artery biopsy ( TAB temporal artery biopsy ) was performed (diagnostic stand
38 ted GCA was examined in peripheral blood and temporal artery biopsies with protein quantification ass
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