review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Lucy C Okell | Q55176208 |
Chris J Drakeley | Q56774786 | ||
Teun Bousema | Q44168464 | ||
Ingrid Felger | Q39408549 | ||
P2860 | cites work | Asymptomatic malaria infections--do they matter? | Q47995672 |
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Global malaria mortality between 1980 and 2010: a systematic analysis | Q20905423 | ||
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Mass drug administration for malaria | Q24201881 | ||
Real-time nucleic acid sequence-based amplification is more convenient than real-time PCR for quantification of Plasmodium falciparum | Q24558561 | ||
The relevance and applicability of oocyst prevalence as a read-out for mosquito feeding assays | Q26315349 | ||
The human malaria parasite Pfs47 gene mediates evasion of the mosquito immune system | Q27973784 | ||
The potential contribution of mass treatment to the control of Plasmodium falciparum malaria | Q28478260 | ||
Mosquito feeding assays to determine the infectiousness of naturally infected Plasmodium falciparum gametocyte carriers | Q28482471 | ||
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Malaria control in Botswana, 2008-2012: the path towards elimination | Q28660568 | ||
A transcriptional switch underlies commitment to sexual development in malaria parasites | Q30041370 | ||
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High heterogeneity in the number of Plasmodium falciparum gametocytes in the bloodmeal of mosquitoes fed on the same host | Q30965521 | ||
Relation between HLA genes, human skin volatiles and attractiveness of humans to malaria mosquitoes | Q44170166 | ||
Submicroscopic Plasmodium falciparum gametocyte densities frequently result in mosquito infection. | Q44171862 | ||
Factors determining the true reservoir of infection of Plasmodium falciparum and Wuchereria bancrofti in a West African village | Q45277732 | ||
Impact of genetic complexity on longevity and gametocytogenesis of Plasmodium falciparum during the dry and transmission-free season of eastern Sudan | Q46448286 | ||
Frequent and persistent, asymptomatic plasmodium falciparum infections in african infants, characterized by multilocus genotyping | Q47877169 | ||
High prevalence of asymptomatic Plasmodium vivax and Plasmodium falciparum infections in native Amazonian populations | Q47911926 | ||
Superiority of preparations from skin scarification over preparations of peripheral blood for the diagnosis of malaria | Q47939496 | ||
Observations on the natural history of malaria in the semi-resistant West African | Q47952742 | ||
The distribution of Plasmodium falciparum infection durations | Q47981171 | ||
Infectivity of asymptomatic Plasmodium-infected human populations to Anopheles dirus mosquitoes in western Thailand | Q33200838 | ||
Dynamics of polymorphism in a malaria vaccine antigen at a vaccine-testing site in Mali | Q33278087 | ||
A review of malaria diagnostic tools: microscopy and rapid diagnostic test (RDT). | Q33312812 | ||
Substantial contribution of submicroscopical Plasmodium falciparum gametocyte carriage to the infectious reservoir in an area of seasonal transmission | Q33520254 | ||
Long-lived antibody and B Cell memory responses to the human malaria parasites, Plasmodium falciparum and Plasmodium vivax | Q33533328 | ||
Stable and unstable malaria hotspots in longitudinal cohort studies in Kenya | Q33631268 | ||
Detectability of Plasmodium falciparum clones | Q33662597 | ||
Rapid and effective malaria control in Cambodia through mass administration of artemisinin-piperaquine | Q33724176 | ||
Revisiting the circulation time of Plasmodium falciparum gametocytes: molecular detection methods to estimate the duration of gametocyte carriage and the effect of gametocytocidal drugs | Q33898575 | ||
A cascade of DNA-binding proteins for sexual commitment and development in Plasmodium | Q33929633 | ||
Detection and quantification of Plasmodium falciparum in blood samples using quantitative nucleic acid sequence-based amplification. | Q33970234 | ||
Single dose primaquine for clearance of Plasmodium falciparum gametocytes in children with uncomplicated malaria in Uganda: a randomised, controlled, double-blind, dose-ranging trial | Q34038938 | ||
Hitting hotspots: spatial targeting of malaria for control and elimination | Q34149880 | ||
Epidemiology and infectivity of Plasmodium falciparum and Plasmodium vivax gametocytes in relation to malaria control and elimination | Q34177472 | ||
Identification of the four human malaria parasite species in field samples by the polymerase chain reaction and detection of a high prevalence of mixed infections | Q34363906 | ||
The dynamics of natural Plasmodium falciparum infections | Q34429326 | ||
Changing malaria epidemiology and diagnostic criteria for Plasmodium falciparum clinical malaria | Q34430949 | ||
Plasmodium sex determination and transmission to mosquitoes | Q34535067 | ||
Ensuring quality and access for malaria diagnosis: how can it be achieved? | Q34557841 | ||
Reactive case detection for malaria elimination: real-life experience from an ongoing program in Swaziland. | Q34735237 | ||
Novel genotyping tools for investigating transmission dynamics of Plasmodium falciparum | Q34736521 | ||
Malaria parasites form filamentous cell-to-cell connections during reproduction in the mosquito midgut. | Q34770683 | ||
Strategies for detection of Plasmodium species gametocytes | Q35061598 | ||
Determinants of heterogeneous blood feeding patterns by Aedes aegypti in Iquitos, Peru | Q35097821 | ||
Thick blood film examination for Plasmodium falciparum malaria has reduced sensitivity and underestimates parasite density | Q35131085 | ||
A cluster-randomized trial of mass drug administration with a gametocytocidal drug combination to interrupt malaria transmission in a low endemic area in Tanzania | Q35203887 | ||
Real-time quantitative reverse transcription PCR for monitoring of blood-stage Plasmodium falciparum infections in malaria human challenge trials | Q35771762 | ||
Plasmodium falciparum malaria in the Peruvian Amazon, a region of low transmission, is associated with immunologic memory | Q35867604 | ||
Operational research to inform a sub-national surveillance intervention for malaria elimination in Solomon Islands | Q35984235 | ||
Host cell deformability is linked to transmission in the human malaria parasite Plasmodium falciparum. | Q36035540 | ||
Factors determining the occurrence of submicroscopic malaria infections and their relevance for control | Q36503207 | ||
The epidemiology of Plasmodium falciparum gametocytes: weapons of mass dispersion | Q36538665 | ||
The impact of hotspot-targeted interventions on malaria transmission: study protocol for a cluster-randomized controlled trial | Q36621479 | ||
A controlled, parallel, cluster-randomized trial of community-wide screening and treatment of asymptomatic carriers of Plasmodium falciparum in Burkina Faso | Q36690099 | ||
Epidemiological significance of repeated infections with homologous and heterologous strains and species of Plasmodium | Q36779328 | ||
Predicting mosquito infection from Plasmodium falciparum gametocyte density and estimating the reservoir of infection | Q36864852 | ||
An intensive longitudinal cohort study of Malian children and adults reveals no evidence of acquired immunity to Plasmodium falciparum infection | Q36892880 | ||
Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics | Q36982630 | ||
Highly sensitive detection of malaria parasitemia in a malaria-endemic setting: performance of a new loop-mediated isothermal amplification kit in a remote clinic in Uganda | Q37037033 | ||
Sex ratio adjustment and kin discrimination in malaria parasites | Q37253816 | ||
Case investigation and reactive case detection for malaria elimination in northern Senegal | Q37359989 | ||
Marked decline in malaria prevalence among pregnant women and their offspring from 1996 to 2010 on the south Kenyan Coast | Q37372620 | ||
Comparison of surveillance methods applied to a situation of low malaria prevalence at rural sites in The Gambia and Guinea Bissau | Q37470249 | ||
Decreased growth rate of P. falciparum blood stage parasitemia with age in a holoendemic population | Q37635135 | ||
The importance of accuracy in diagnosis of positive malaria cases in a country progressing towards malaria elimination | Q37645755 | ||
A micro-epidemiological analysis of febrile malaria in Coastal Kenya showing hotspots within hotspots | Q37723182 | ||
The changing epidemiology of malaria elimination: new strategies for new challenges | Q38099695 | ||
Asymptomatic parasitaemia as a risk factor for symptomatic malaria in a cohort of Ugandan children | Q38881807 | ||
Molecular evaluation of the natural history of asymptomatic parasitemia in Ugandan children | Q38882004 | ||
Identification of hot spots of malaria transmission for targeted malaria control | Q38917779 | ||
Parasite multiplication potential and the severity of Falciparum malaria | Q38945841 | ||
Filter paper collection of Plasmodium falciparum mRNA for detecting low-density gametocytes | Q39110719 | ||
Age and seasonal variation in the transition rates and detectability of Plasmodium falciparum malaria | Q39426344 | ||
A retrospective examination of sporozoite- and trophozoite-induced infections with Plasmodium falciparum in patients previously infected with heterologous species of Plasmodium: effect on development of parasitologic and clinical immunity | Q40635092 | ||
Plasmodium falciparum gametocytes: their longevity and infectivity | Q40752602 | ||
Characteristics of Plasmodium falciparum parasites that survive the lengthy dry season in eastern Sudan where malaria transmission is markedly seasonal | Q41925339 | ||
Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study | Q41932967 | ||
Substantially reduced pre-patent parasite multiplication rates are associated with naturally acquired immunity to Plasmodium falciparum | Q42127731 | ||
Residual Plasmodium falciparum parasitemia in Kenyan children after artemisinin-combination therapy is associated with increased transmission to mosquitoes and parasite recurrence | Q42127740 | ||
Submicroscopic Plasmodium falciparum gametocyte carriage is common in an area of low and seasonal transmission in Tanzania | Q43736591 | ||
Genetic variation in human HBB is associated with Plasmodium falciparum transmission | Q43931035 | ||
Age-dependent distribution of Plasmodium falciparum gametocytes quantified by Pfs25 real-time QT-NASBA in a cross-sectional study in Burkina Faso | Q43932772 | ||
High human malarial infectivity to laboratory-bred Anopheles gambiae in a village in Burkina Faso. | Q43936049 | ||
Daily dynamics of Plasmodium falciparum subpopulations in asymptomatic children in a holoendemic area | Q43953181 | ||
High gametocyte complexity and mosquito infectivity of Plasmodium falciparum in the Gambia | Q44137417 | ||
Local-scale variation in malaria infection amongst rural Gambian children estimated by satellite remote sensing | Q44143530 | ||
Infectious reservoir of Plasmodium vivax and Plasmodium falciparum malaria in an endemic region of Sri Lanka | Q44144653 | ||
Short-range attractiveness of pregnant women to Anopheles gambiae mosquitoes | Q44148115 | ||
Testing vaccines in human experimental malaria: statistical analysis of parasitemia measured by a quantitative real-time polymerase chain reaction | Q44161485 | ||
Moderate effect of artemisinin-based combination therapy on transmission of Plasmodium falciparum | Q44167789 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | public health | Q189603 |
malaria | Q12156 | ||
P304 | page(s) | 833-840 | |
P577 | publication date | 2014-10-20 | |
P1433 | published in | Nature Reviews Microbiology | Q1071797 |
P1476 | title | Asymptomatic malaria infections: detectability, transmissibility and public health relevance | |
P478 | volume | 12 |