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1 shmania major (cutaneous leishmaniasis), and Plasmodium falciparum (malaria).
2 transmission-blocking vaccines (TBV) against Plasmodium falciparum malaria.
3 dothelium are central to the pathogenesis of Plasmodium falciparum malaria.
4 gans plays a key role in the pathogenesis of Plasmodium falciparum malaria.
5 on genetics simulators cannot suitably model Plasmodium falciparum malaria.
6 tment in pregnancy (IPTp) is used to prevent Plasmodium falciparum malaria.
7 development of an effective vaccine against Plasmodium falciparum malaria.
8 hain, protects West African children against Plasmodium falciparum malaria.
9 more effective liver-stage vaccines against Plasmodium falciparum malaria.
10 ed-species infections protect against severe Plasmodium falciparum malaria.
11 (AMA-1) is a promising vaccine candidate for Plasmodium falciparum malaria.
12 are the population most severely affected by Plasmodium falciparum malaria.
13 NF) has been linked with the pathogenesis of Plasmodium falciparum malaria.
14 tistage, multigene DNA-based vaccine against Plasmodium falciparum malaria.
15 sfunction are common complications of severe Plasmodium falciparum malaria.
16 ntly needed to stem the global resurgence of Plasmodium falciparum malaria.
17 re important mediators of protection against Plasmodium falciparum malaria.
18 with hemoglobin variants in areas of endemic Plasmodium falciparum malaria.
19 n life as a "natural vaccine" against severe Plasmodium falciparum malaria.
20 malaria, especially of chloroquine-resistant Plasmodium falciparum malaria.
21 nized NOD-scid IL-2Rgammanull mouse model of Plasmodium falciparum malaria.
22 t the effects of ID on antibody responses to Plasmodium falciparum malaria.
23 000s have dramatically reduced the burden of Plasmodium falciparum malaria.
24 amodiaquine is widely used for uncomplicated Plasmodium falciparum malaria.
25 Infants are protected against Plasmodium falciparum malaria.
26 uired to combat the spread of drug-resistant Plasmodium falciparum malaria.
27 d between Malawian children with CM and mild Plasmodium falciparum malaria.
28 oughout sub-Saharan Africa (SSA) to diagnose Plasmodium falciparum malaria.
29 cells (RBCs) contributes to pathogenesis in Plasmodium falciparum malaria.
30 apies (ACTs) threatens the global control of Plasmodium falciparum malaria.
31 in the context of acquired immunity against Plasmodium falciparum malaria.
32 -Saharan Africa in adults with uncomplicated Plasmodium falciparum malaria.
33 could be considered for rescue treatment for Plasmodium falciparum malaria.
34 otect children from severe and uncomplicated Plasmodium falciparum malaria.
35 most efficacious treatment of uncomplicated Plasmodium falciparum malaria.
36 w era in effectively treating drug-resistant Plasmodium falciparum malaria.
37 859 patients aged 6 months to 12 years with Plasmodium falciparum malaria.
38 eases and obesity, is associated with severe Plasmodium falciparum malaria.
39 rison to results of PCR for the detection of Plasmodium falciparum malaria.
40 therapy (ACT) is the first-line treatment of Plasmodium falciparum malaria.
41 could be considered for rescue treatment for Plasmodium falciparum malaria.
42 t on ART, all of whom required treatment for Plasmodium falciparum malaria.
43 sis before, during, and after infection with Plasmodium falciparum malaria.
44 bstantial reduction in deaths resulting from Plasmodium falciparum malaria.
45 ine treatment against confirmed or suspected Plasmodium falciparum malaria.
46 ered as a means to interrupt transmission of Plasmodium falciparum malaria.
47 es a serious threat to the global control of Plasmodium falciparum malaria.
48 d of care for the treatment of uncomplicated Plasmodium falciparum malaria.
49 trophil function in 58 Gambian children with Plasmodium falciparum malaria [55 (95%) with uncomplicat
50 te in Mozambican children with uncomplicated Plasmodium falciparum malaria 7 days after combination t
54 se-control study of 996 children with severe Plasmodium falciparum malaria and 1220 community control
55 ignificant protection against infection with Plasmodium falciparum malaria and also against clinical
57 n Africa for the management of uncomplicated Plasmodium falciparum malaria and for chemoprevention st
58 plasma samples from patients with confirmed Plasmodium falciparum malaria and in human whole-blood s
60 one that is widely used to prevent and clear Plasmodium falciparum malaria and Pneumocystis jirovecii
61 used to parameterize mechanistic models for Plasmodium falciparum malaria and reliably predict the e
64 disease, previous history of preterm birth, Plasmodium falciparum malaria, and any helmintic infecti
65 ty to most NTDs neglected tropical diseases, Plasmodium falciparum malaria, and enteric pathogens, bu
66 stance is a major obstacle to the control of Plasmodium falciparum malaria, and its origins and modes
69 le cell traits confer protection from severe Plasmodium falciparum malaria are not yet fully elucidat
70 e public health and economic consequences of Plasmodium falciparum malaria are once again regarded as
74 1 (AMA1) is a leading vaccine candidate for Plasmodium falciparum malaria, as antibodies against rec
75 group has relatively better protection from Plasmodium falciparum malaria, as reflected by fewer sym
77 nce of the spatiotemporal prevalence of both Plasmodium falciparum malaria-attributable and non-malar
78 alling is essential for the proliferation of Plasmodium falciparum malaria blood stage parasites.
79 ay of the current treatment of uncomplicated Plasmodium falciparum malaria, but ACT resistance is spr
81 ne treatment recommended by the WHO to treat Plasmodium falciparum malaria, but clinical resistance a
82 ait (HbAS) is known to be protective against Plasmodium falciparum malaria, but it is unclear when du
83 e highly effective at treating uncomplicated Plasmodium falciparum malaria, but the emergence of the
84 ncy is believed to confer protection against Plasmodium falciparum malaria, but the precise nature of
85 howed modest efficacy of the vaccine against Plasmodium falciparum malaria, but was not powered to as
86 le-cell trait) or HbC (HbAC) protect against Plasmodium falciparum malaria by unclear mechanisms.
89 icant peaks in 2010; examples were increased Plasmodium falciparum malaria (chi(2)=37.57, p<0.001); i
91 bC) are well known to protect against severe Plasmodium falciparum malaria, conclusive evidence on th
98 land, Oreg.), to detect Plasmodium vivax and Plasmodium falciparum malaria during an outbreak in Hond
100 e a significant negative association between Plasmodium falciparum malaria endemicity and LTL while a
103 tive, first-line treatment for uncomplicated Plasmodium falciparum malaria, except in the first trime
105 Malaria Meta-Signature, which discriminates Plasmodium falciparum malaria from uninfected controls;
109 ntury, successful antifolate therapy against Plasmodium falciparum malaria has been attributed to hos
112 in regulating host immunity in children with Plasmodium falciparum malaria has not previously been re
114 ens may be able to confer protection against Plasmodium falciparum malaria; however, a technology for
115 isinins have revolutionized the treatment of Plasmodium falciparum malaria; however, resistance threa
116 gold standard choice to treat uncomplicated Plasmodium falciparum malaria; however, they are hydroph
118 n dengue hemorrhagic fever in Bangkok and of Plasmodium falciparum malaria in a highland area of west
121 nation therapy (ACT) for multidrug-resistant Plasmodium falciparum malaria in Cambodia because of few
122 09, 687 of 2885 patients (23.8%) treated for Plasmodium falciparum malaria in clinical studies in Mya
125 attributed to the resistance it provides to Plasmodium falciparum malaria in its heterozygous state,
127 s have successfully reduced the incidence of Plasmodium falciparum malaria in many areas, there has b
129 and HbAC are hypothesized to protect against Plasmodium falciparum malaria in part by enhancing natur
130 s the first-line treatment for uncomplicated Plasmodium falciparum malaria in response to failing SP
131 ual spraying and other interventions against Plasmodium falciparum malaria in seasonal settings in Af
135 he recent emergence of artemisinin-resistant Plasmodium falciparum malaria in western Cambodia could
137 able malaria transmission, susceptibility to Plasmodium falciparum malaria increases during first pre
138 As the prevalence of artemisinin-resistant Plasmodium falciparum malaria increases in the Greater M
139 nstrate this with four examples: identifying Plasmodium falciparum malaria-infected erythrocytes in a
140 ia (CM) is a severe clinical complication of Plasmodium falciparum malaria infection and is character
141 aged 6 months to 14 years were assessed for Plasmodium falciparum malaria infection by rapid diagnos
148 evalence of PCR-confirmed non-falciparum and Plasmodium falciparum malaria infections within a longit
169 and vaccine-induced immunity to blood-stage Plasmodium falciparum malaria is of long-standing intere
170 g pregnant women with protective immunity to Plasmodium falciparum malaria is often dominated by VAR2
171 Mass drug administration for elimination of Plasmodium falciparum malaria is recommended by WHO in s
173 The development of clinical immunity to Plasmodium falciparum malaria is thought to require year
174 -based combination therapies (ACTs) to treat Plasmodium falciparum malaria is threatened by resistanc
176 lability and accuracy of our software on 245 Plasmodium falciparum malaria isolates from three contin
177 uitoes, the world's most important vector of Plasmodium falciparum malaria, locate their human hosts
178 dren, aged 3 months to 14 years, with severe Plasmodium falciparum malaria matched to uncomplicated m
179 emisinin-based combination therapy (ACT) for Plasmodium falciparum malaria may be threatened by paras
187 -specific system of genetic integration into Plasmodium falciparum malaria parasite chromosomes.
188 independent host-parasite interaction in the Plasmodium falciparum malaria parasite invasion of RBCs.
189 ortholog of Pfs47, a protein that allows the Plasmodium falciparum malaria parasite to evade mosquito
190 and anti-malarial resistance has enabled the Plasmodium falciparum malaria parasite to inflict high m
192 stereomers 5a and 5c showed activity against Plasmodium falciparum malaria parasites (IC50 approximat
193 abolic output of the apicoplast organelle in Plasmodium falciparum malaria parasites and is required
194 tanding the genomic diversity of circulating Plasmodium falciparum malaria parasites can assist infec
198 K13-mediated artemisinin (ART) resistance in Plasmodium falciparum malaria parasites has led to wides
199 opy to investigate structural development of Plasmodium falciparum malaria parasites in normal and ge
200 ization has been implicated in the growth of Plasmodium falciparum malaria parasites in their Anophel
208 These districts border Myanmar which harbors Plasmodium falciparum malaria parasites resistant to art
212 of a cell-free lysate prepared from asexual Plasmodium falciparum malaria parasites to remove uracil
214 high antimalarial potencies in vitro against Plasmodium falciparum malaria parasites, and furans 5a a
216 ein, fatty acids, anionic phospholipids, and Plasmodium falciparum malaria parasitized erythrocytes.
217 Severe anemia is a lethal complication of Plasmodium falciparum malaria, particularly in children.
218 t surface antigens play an important role in Plasmodium falciparum malaria pathogenesis and in immune
219 3 (SOD3) was significantly elevated in both Plasmodium falciparum malaria patients and mice infected
220 uinone that is used therapeutically to treat Plasmodium falciparum malaria, Pneumocystis carinii pneu
221 ne that is used therapeutically for treating Plasmodium falciparum malaria, Pneumocystis jirovecii pn
222 rammatic use of the R21/Matrix-M vaccine for Plasmodium falciparum malaria prevention in children liv
232 f adjunct or anti-disease therapy for severe Plasmodium falciparum malaria requires cellular and mole
234 umefantrine is widely used for uncomplicated Plasmodium falciparum malaria; sulfadoxine-pyrimethamine
237 ally conducted to identify studies on severe Plasmodium falciparum malaria that included information
238 primary marker of artemisinin resistance in Plasmodium falciparum malaria that threatens the long-te
240 ut on 279 children with severe anemia due to Plasmodium falciparum malaria; the results were similar
241 n G6PD deficiency and severe and complicated Plasmodium falciparum malaria through a case-control stu
243 The emergence and spread of resistance in Plasmodium falciparum malaria to artemisinin combination
244 a mathematical model of the transmission of Plasmodium falciparum malaria to explore the potential e
245 alyses comparing clinical subtypes of severe Plasmodium falciparum malaria to matched controls with u
247 sed malaria elimination project to interrupt Plasmodium falciparum malaria transmission in a rural di
248 ng progress has been seen with reductions in Plasmodium falciparum malaria transmission in some parts
249 Zambia has experienced a dramatic decline in Plasmodium falciparum malaria transmission in the past d
250 a were analyzed with network analysis tools, Plasmodium falciparum malaria transmission maps, and glo
252 returned to the UK from Uganda in 2022 with Plasmodium falciparum malaria, twice failed treatment wi
253 Anopheles gambiae mosquitoes that transmit Plasmodium falciparum malaria use a series of olfactory
254 es gambiae mosquito, which is the vector for Plasmodium falciparum malaria, uses a series of olfactor
255 te load in individual subjects infected with Plasmodium falciparum malaria, using only data obtained
257 ein homologue 5 (RH5), a leading blood-stage Plasmodium falciparum malaria vaccine target, interacts
258 T molecular marker for chloroquine-resistant Plasmodium falciparum malaria was retrospectively measur
259 l bloodstream infection and 35 children with Plasmodium falciparum malaria were analyzed using protei
262 erapy on transmission, Gambian children with Plasmodium falciparum malaria were treated with standard
263 f uncomplicated malaria, and 687 episodes of Plasmodium falciparum malaria were treated with study dr
264 A total of 577 episodes of uncomplicated Plasmodium falciparum malaria were treated with study dr
266 ogy, and not least in protective immunity to Plasmodium falciparum malaria, where key antigens show s
270 , 48, and 72 hours) in African children with Plasmodium falciparum malaria with a prespecified delta
271 years, who were treated for 249 episodes of Plasmodium falciparum malaria with artemether-lumefantri
272 causal (ie, pre-erythrocytic) prophylaxis of Plasmodium falciparum malaria with prolonged activity wo
273 the influence of climate on the incidence of Plasmodium falciparum malaria worldwide and how it might
275 endemic areas, children suffer the most from Plasmodium falciparum malaria, yet newborns and young in