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1 or the effect of ALB on clearance of CFA and microfilaremia.
2 f circulating filarial antigenemia (CFA) and microfilaremia.
3 he target population) were tested for L. loa microfilaremia.
4 r role in both the presence and intensity of microfilaremia.
5 r the detection and quantification of L. loa microfilaremia.
6 were more common in study participants with microfilaremia (33.4% versus 11.1%, P < 0.001) and more
11 ing characteristic curve [AUROC] = 0.73) and microfilaremia (AUROC = 0.84) by a random forest machine
12 assessed for both W. bancrofti infection and microfilaremia by controlling for individual risk factor
15 Patent infections with long-term, high-grade microfilaremia do not develop in nonendemic individuals.
16 R was equally sensitive for the detection of microfilaremia due to Wuchereria bancrofti (2 of 46 samp
17 o infection with Wuchereria bancrofti and to microfilaremia in a village of the Republic of Congo.
18 tment-naive adults with Wuchereria bancrofti microfilaremia in Agboville district of Cote d'Ivoire we
19 tment-naive adults with Wuchereria bancrofti microfilaremia in Cote d'Ivoire were randomized to recei
20 Antibody reactivity was detectable before microfilaremia in experimentally infected rhesus monkeys
22 ly constant for the subjects with persistent microfilaremia (Mf(+/+)), in contrast to sharp decreases
24 d mice, particularly those that did not have microfilaremia (Mf(-)), had more severe anemia and loss
25 mum permissible level of NT for which the 1% microfilaremia (mf) prevalence threshold can be achieved
27 states, including occult loiasis (n = 148), microfilaremia (n = 42), or both (n = 84), compared to 1
28 ug treatment regimens capable of suppressing microfilaremia to very low levels, along with improvemen
30 5) were associated with antigenemia, whereas microfilaremia was associated with significantly decreas