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1 (IPTp)-is known to exhibit activity against Schistosoma haematobium.
2 arlier compared with Schistosoma mansoni and Schistosoma haematobium.
3 sed from the parasitic trematode blood fluke Schistosoma haematobium.
4 imary structure of acetylcholinesterase from Schistosoma haematobium.
5 , 1 each with endemic Schistosoma mansoni or Schistosoma haematobium.
6 nfection with either Wuchereria bancrofti or Schistosoma haematobium.
7 , in turn, reduces morbidity is proposed for Schistosoma haematobium, a parasite of major public heal
9 spot prevalence), and a regression model for Schistosoma haematobium achieves 90% sensitivity, 90% sp
10 compared patterns of recognition of defined Schistosoma haematobium adult worm antigens by serum ant
11 osomiasis, caused by the parasitic trematode Schistosoma haematobium, affects over 112 million people
12 humans infected with Schistosoma mansoni and Schistosoma haematobium and considers the practical impl
13 considered as reference diagnostic tests for Schistosoma haematobium and Schistosoma mansoni infectio
15 NA encoding the AChE from the human parasite Schistosoma haematobium and succeeded in expressing func
16 the distribution of Schistosoma mansoni and Schistosoma haematobium and the incidence of schistosomi
17 sthorchis viverrini, Clonorchis sinensis and Schistosoma haematobium are classified as Group 1 biolog
18 thorchis viverrini, Clonorchis sinensis, and Schistosoma haematobium are classified as group 1 biolog
20 aran Africa show that genital infection with Schistosoma haematobium [corrected] may increase the ris
22 portion of participants who had at least one Schistosoma haematobium egg observed on light microscopy
23 ence of heavy-intensity infections (ie, >=50 Schistosoma haematobium eggs per 10 mL of urine or >=400
25 eins recognized by pooled serum samples from Schistosoma haematobium-exposed Zimbabweans were determi
26 system schistosomiasis due to infection with Schistosoma haematobium following recreational water exp
28 ention packages to interrupt transmission of Schistosoma haematobium in a seasonal transmission setti
30 recently published study, which included 163 Schistosoma haematobium-infected individuals and 183 mat
33 d 7-12-y-old anemic children with documented Schistosoma haematobium infection (n = 224 for AGP, CRP,
34 s consistent with observed field patterns of Schistosoma haematobium infection and antibody responses
35 al profiles in people with or without active Schistosoma haematobium infection and to determine wheth
37 assessed whether bladder pathology in human Schistosoma haematobium infection is related to the bala
40 sition than females without, particularly in Schistosoma haematobium infection, and a greater risk of
50 Urogenital schistosomiasis, infection with Schistosoma haematobium, is linked to increased risk for
52 identified Schistosoma mattheei nuclear and Schistosoma haematobium mitochondrial DNA, indicative of
53 how the cervical environment is impacted by Schistosoma haematobium or Schistosoma mansoni infection
54 , neutralizing anti-IL-10 added to PBMC from Schistosoma haematobium patients' enhanced adult worm (S
56 ur change interventions for the reduction of Schistosoma haematobium prevalence and infection intensi
57 ical digital detection and quantification of Schistosoma haematobium provided by AiDx NTDx multi-diag
58 ails host the most common human blood fluke, Schistosoma haematobium, responsible for approximately t
59 young adults were recruited from areas where Schistosoma haematobium (S.h) infections were high or lo
60 lated from 12 patients showed infection with Schistosoma haematobium, S haematobium-Schistosoma bovis
61 Belgian travelers returned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infecti
64 CATSH, a CRISPR-assisted diagnostic test for Schistosoma haematobium, utilising recombinase polymeras
66 cted tropical disease caused by the parasite Schistosoma haematobium, which resides in the vasculatur
67 Africa, 112 million people are infected with Schistosoma haematobium, with the most intense infection
68 trongly associated with increasing levels of Schistosoma haematobium worm IgG1, with adolescents with
70 n urogenital schistosomiasis, infection with Schistosoma haematobium worms, remains poorly understood
71 es urinary tract coinfection by bacteria and Schistosoma haematobium worms, the etiologic agent of ur