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Global Epidemiology of Plasmodium vivax
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Online Biomedical Resources for Malaria‐Related Red Cell Disorders
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Paludrine treatment of experimental malaria infection; effective minimum doses
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A strain of Plasmodium vivax characterized by prolonged incubation: the effect of numbers of sporozoites on the length of the prepatent period
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Hereditary ovalocytosis and reduced susceptibility to malaria in Papua New Guinea
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Permethrin-impregnated bed nets for the prevention of malaria in schoolchildren on the Thai-Burmese border
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The Global Public Health Significance of Plasmodium vivax
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Chemotherapeutic Strategies for Reducing Transmission of Plasmodium vivax Malaria
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Control and Elimination of Plasmodium vivax
inferredcites →https://doi.org/10.1016/b978-0-12-407826-0.00002-3openalex-snapshot
Red Blood Cell Polymorphism and Susceptibility to Plasmodium vivax
inferredcites →https://doi.org/10.1016/b978-0-12-407826-0.00003-5openalex-snapshot
Natural Acquisition of Immunity to Plasmodium vivax
inferredcites →https://doi.org/10.1016/j.ijpddr.2011.08.001openalex-snapshot
Phenotyping clinical resistance to chloroquine in Plasmodium vivax in northeastern Papua, Indonesia
inferredcites →https://doi.org/10.1016/j.pt.2004.02.001openalex-snapshot
Plasmodium vivax transmission: chances for control?
inferredcites →https://doi.org/10.1016/j.pt.2004.03.006openalex-snapshot
Mixed-species malaria infections in humans
inferredcites →https://doi.org/10.1016/j.pt.2007.04.009openalex-snapshot
Plasmodium malariae and Plasmodium ovale – the ‘bashful’ malaria parasites
inferredcites →https://doi.org/10.1016/j.pt.2007.08.011openalex-snapshot
Neglect of Plasmodium vivax malaria
inferredcites →https://doi.org/10.1016/j.trstmh.2006.06.008openalex-snapshot
Therapeutic response of multidrug-resistant Plasmodium falciparum and P. vivax to chloroquine and sulfadoxine–pyrimethamine in southern Papua, Indonesia
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Epidemiology and control of frontier malaria in Brazil: lessons from community-based studies in rural Amazonia
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Associations of peak shifts in age-prevalence for human malarias with bednet coverage
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The epidemiology of severe malaria in an area of low transmission in Thailand
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Determining Global Population Distribution: Methods, Applications and Data
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An unexpected cause of fever and seizures
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Operational strategies to achieve and maintain malaria elimination
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Shrinking the malaria map: progress and prospects
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Eliminating malaria—all of them
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Relation between falciparum malaria and bacteraemia in Kenyan children: a population-based, case-control study and a longitudinal study
inferredcites →https://doi.org/10.1016/s0140-6736(13)60310-4openalex-snapshot
The changing epidemiology of malaria elimination: new strategies for new challenges
inferredcites →https://doi.org/10.1016/s0140-6736(89)91792-3openalex-snapshot
PLASMODIUM VIVAX RESISTANCE TO CHLOROQUINE?
inferredcites →https://doi.org/10.1016/s1471-4922(03)00005-9openalex-snapshot
Can primaquine therapy for vivax malaria be improved?
inferredcites →https://doi.org/10.1016/s1473-3099(07)70021-xopenalex-snapshot
Epidemiology and burden of malaria in pregnancy
inferredcites →https://doi.org/10.1016/s1473-3099(07)70022-1openalex-snapshot
Malaria in pregnancy: pathogenesis and immunity
inferredcites →https://doi.org/10.1016/s1473-3099(09)70177-xopenalex-snapshot
Key gaps in the knowledge of Plasmodium vivax, a neglected human malaria parasite
inferredcites →https://doi.org/10.1016/s1473-3099(10)70079-7openalex-snapshot
Artemisinin combination therapy for vivax malaria
inferredcites →https://doi.org/10.1016/s1473-3099(11)70315-2openalex-snapshot
Malaria in pregnancy in the Asia-Pacific region
inferredcites →https://doi.org/10.1016/s1473-3099(11)70339-5openalex-snapshot
Adverse effects of falciparum and vivax malaria and the safety of antimalarial treatment in early pregnancy: a population-based study
inferredcites →https://doi.org/10.1016/s1473-3099(13)70095-1openalex-snapshot
The activation of vivax malaria hypnozoites by infectious diseases
inferredcites →https://doi.org/10.1016/s1473-3099(14)70855-2openalex-snapshot
Global extent of chloroquine-resistant Plasmodium vivax: a systematic review and meta-analysis
inferredcites →https://doi.org/10.1017/s0031182000080227openalex-snapshot
Interactions between malaria parasites infecting the same vertebrate host
inferredcites →https://doi.org/10.1017/s0031182015001249openalex-snapshot
Immunity to malaria in an era of declining malaria transmission
inferredcites →https://doi.org/10.1038/383522a0openalex-snapshot
High incidence of malaria in α-thalassaemic children
inferredcites →https://doi.org/10.1038/nature12060openalex-snapshot
The global distribution and burden of dengue
inferredcites →https://doi.org/10.1038/nature15535openalex-snapshot
The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015
inferredcites →https://doi.org/10.1038/ncomms1104openalex-snapshot
Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis
inferredcites →https://doi.org/10.1038/ncomms1265openalex-snapshot
The global distribution of the Duffy blood group
inferredcites →https://doi.org/10.1038/ncomms2241openalex-snapshot
Factors determining the occurrence of submicroscopic malaria infections and their relevance for control
inferredcites →https://doi.org/10.1038/ncomms9170openalex-snapshot
Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria
inferredcites →https://doi.org/10.1038/nm0111-48openalex-snapshot
Defying malaria: Fathoming severe Plasmodium vivax disease
inferredcites →https://doi.org/10.1038/sdata.2015.12openalex-snapshot
Global database of matched Plasmodium falciparum and P. vivax incidence and prevalence records from 1985–2013
inferredcites →https://doi.org/10.1056/nejmc1301936openalex-snapshot
Primaquine Failure and Cytochrome P-450 2D6 in Plasmodium vivax Malaria
inferredcites →https://doi.org/10.1056/nejmoa0804915openalex-snapshot
A Trial of Combination Antimalarial Therapies in Children from Papua New Guinea
inferredcites →https://doi.org/10.1073/pnas.0910142106openalex-snapshot
Interaction of malaria with a common form of severe thalassemia in an Asian population
inferredcites →https://doi.org/10.1073/pnas.0912496107openalex-snapshot
Plasmodium vivax clinical malaria is commonly observed in Duffy-negative Malagasy people
inferredcites →https://doi.org/10.1080/00034983.1990.11812429openalex-snapshot
Consequences of maternal anaemia on outcome of pregnancy in a malaria endemic area in Papua New Guinea
inferredcites →https://doi.org/10.1086/432519openalex-snapshot
How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria
inferredcites →https://doi.org/10.1086/512241openalex-snapshot
Relapses ofPlasmodium vivaxInfection Usually Result from Activation of Heterologous Hypnozoites
inferredcites →https://doi.org/10.1086/586743openalex-snapshot
Adverse Pregnancy Outcomes in an Area Where Multidrug‐Resistant Plasmodium vivax and Plasmodium falciparum Infections Are Endemic
inferredcites →https://doi.org/10.1086/599041openalex-snapshot
Vivax Malaria: A Major Cause of Morbidity in Early Infancy
inferredcites →https://doi.org/10.1093/cid/ciq249openalex-snapshot
Plasmodium vivax Recurrence Following Falciparum and Mixed Species Malaria: Risk Factors and Effect of Antimalarial Kinetics
inferredcites →https://doi.org/10.1093/cid/cis615openalex-snapshot
Postmortem Characterization of Patients With Clinical Diagnosis of Plasmodium vivax Malaria: To What Extent Does This Parasite Kill?
inferredcites →https://doi.org/10.1093/infdis/jis580openalex-snapshot
Relapses Contribute Significantly to the Risk of Plasmodium vivax Infection and Disease in Papua New Guinean Children 1–5 Years of Age
inferredcites →https://doi.org/10.1093/infdis/jiu487openalex-snapshot
Severe Malarial Thrombocytopenia: A Risk Factor for Mortality in Papua, Indonesia
inferredcites →https://doi.org/10.1093/qjmed/90.12.751openalex-snapshot
Plasmodium vivax: a cause of malnutrition in young children
inferredcites →https://doi.org/10.1097/qco.0000000000000191openalex-snapshot
Malaria diagnosis for malaria elimination
inferredcites →https://doi.org/10.1097/qco.0b013e32832f14c1openalex-snapshot
New developments in Plasmodium vivax malaria: severe disease and the rise of chloroquine resistance
inferredcites →https://doi.org/10.1126/science.1178849openalex-snapshot
Positively Selected G6PD -Mahidol Mutation Reduces Plasmodium vivax Density in Southeast Asians
inferredcites →https://doi.org/10.1128/aac.01296-10openalex-snapshot
Resistance to Chloroquine Unhinges Vivax Malaria Therapeutics
inferredcites →https://doi.org/10.1128/aac.01879-12openalex-snapshot
Randomized, Open-Label Trial of Primaquine against Vivax Malaria Relapse in Indonesia
inferredcites →https://doi.org/10.1128/aac.48.11.4075-4083.2004openalex-snapshot
Chloroquine Resistance inPlasmodium vivax
inferredcites →https://doi.org/10.1128/cmr.00051-10openalex-snapshot
Epidemiology and Infectivity of Plasmodium falciparum and Plasmodium vivax Gametocytes in Relation to Malaria Control and Elimination
inferredcites →https://doi.org/10.1128/cmr.00074-12openalex-snapshot
Evidence and Implications of Mortality Associated with Acute Plasmodium vivax Malaria
inferredcites →https://doi.org/10.1128/jcm.03437-12openalex-snapshot
High Prevalence of Asymptomatic Malaria in a Tribal Population in Eastern India
inferredcites →https://doi.org/10.1155/2013/520181openalex-snapshot
Concurrent Infection with Dengue and Malaria: An Unusual Presentation
inferredcites →https://doi.org/10.1179/027249309x12547917868808openalex-snapshot
Severe and fatal vivax malaria challenges 'benign tertian malaria' dogma
inferredcites →https://doi.org/10.1186/1471-2334-13-117openalex-snapshot
Endotoxaemia is common in children with Plasmodium falciparummalaria
inferredcites →https://doi.org/10.1186/1475-2875-10-297openalex-snapshot
Determinants of relapse periodicity in Plasmodium vivax malaria
inferredcites →https://doi.org/10.1186/1475-2875-10-378openalex-snapshot
A new world malaria map: Plasmodium falciparum endemicity in 2010
inferredcites →https://doi.org/10.1186/1475-2875-10-90openalex-snapshot
Activation of the hypnozoite: a part of Plasmodium vivax life cycle and survival
inferredcites →https://doi.org/10.1186/1475-2875-11-101openalex-snapshot
Operational research to inform a sub-national surveillance intervention for malaria elimination in Solomon Islands
inferredcites →https://doi.org/10.1186/1475-2875-11-12openalex-snapshot
Understanding the clinical spectrum of complicated Plasmodium vivax malaria: a systematic review on the contributions of the Brazilian literature
inferredcites →https://doi.org/10.1186/1475-2875-11-135openalex-snapshot
The anaemia of Plasmodium vivax malaria
inferredcites →https://doi.org/10.1186/1475-2875-11-403openalex-snapshot
The effects of urbanization on global Plasmodium vivax malaria transmission
inferredcites →https://doi.org/10.1186/1475-2875-12-361openalex-snapshot
Risk factors associated with slide positivity among febrile patients in a conflict zone of north-eastern Myanmar along the China-Myanmar border
inferredcites →https://doi.org/10.1186/1475-2875-12-42openalex-snapshot
Progress towards malaria elimination in Sabang Municipality, Aceh, Indonesia
inferredcites →https://doi.org/10.1186/1475-2875-13-139openalex-snapshot
Mind the gaps - the epidemiology of poor-quality anti-malarials in the malarious world - analysis of the WorldWide Antimalarial Resistance Network database
inferredcites →https://doi.org/10.1186/1475-2875-13-144openalex-snapshot
Geographical variation in Plasmodium vivax relapse
inferredcites →https://doi.org/10.1186/1475-2875-13-211openalex-snapshot
Challenges in universal coverage and utilization of insecticide-treated bed nets in migrant plantation workers in Myanmar
inferredcites →https://doi.org/10.1186/1475-2875-13-330openalex-snapshot
Characterizing, controlling and eliminating residual malaria transmission
inferredcites →https://doi.org/10.1186/1475-2875-13-481openalex-snapshot
Severe vivax malaria: a systematic review and meta-analysis of clinical studies since 1900
inferredcites →https://doi.org/10.1186/1475-2875-13-488openalex-snapshot
The clinical and public health problem of relapse despite primaquine therapy: case review of repeated relapses of Plasmodium vivax acquired in Papua New Guinea
inferredcites →https://doi.org/10.1186/1475-2875-5-121openalex-snapshot
Comparison of PCR and microscopy for the detection of asymptomatic malaria in a Plasmodium falciparum/vivax endemic area in Thailand
inferredcites →https://doi.org/10.1186/1475-2875-5-15openalex-snapshot
Are insecticide-treated bednets more protective against Plasmodium falciparum than Plasmodium vivax- infected mosquitoes?
inferredcites →https://doi.org/10.1186/1475-2875-6-131openalex-snapshot
Standardizing estimates of the Plasmodium falciparum parasite rate
inferredcites →https://doi.org/10.1186/1475-2875-6-17openalex-snapshot
Assembling a global database of malaria parasite prevalence for the Malaria Atlas Project
inferredcites →https://doi.org/10.1186/1475-2875-7-99openalex-snapshot
Longitudinal study of Plasmodium falciparum and Plasmodium vivax in a Karen population in Thailand
inferredcites →https://doi.org/10.1186/1475-2875-7-s1-s8openalex-snapshot
The role of anti-malarial drugs in eliminating malaria
inferredcites →https://doi.org/10.1186/1475-2875-7-s1-s9openalex-snapshot
Plasmodium vivax: who cares?
inferredcites →https://doi.org/10.1186/1475-2875-8-186openalex-snapshot
Defining the relationship between Plasmodium falciparum parasite rate and clinical disease: statistical models for disease burden estimation
inferredcites →https://doi.org/10.1186/1475-2875-8-41openalex-snapshot
High sensitivity detection of Plasmodium species reveals positive correlations between infections of different species, shifts in age distribution and reduced local variation in Papua New Guinea
inferredcites →https://doi.org/10.1186/1475-2875-9-108openalex-snapshot
Sub-microscopic malaria cases and mixed malaria infection in a remote area of high malaria endemicity in Rattanakiri province, Cambodia: implication for malaria elimination
inferredcites →https://doi.org/10.1186/1475-2875-9-254openalex-snapshot
A large proportion of asymptomatic Plasmodium infections with low and sub-microscopic parasite densities in the low transmission setting of Temotu Province, Solomon Islands: challenges for malaria diagnostics in an elimination setting
inferredcites →https://doi.org/10.1186/1756-3305-3-117openalex-snapshot
The dominant Anopheles vectors of human malaria in Africa, Europe and the Middle East: occurrence data, distribution maps and bionomic précis
inferredcites →https://doi.org/10.1186/1756-3305-3-72openalex-snapshot
The dominant Anopheles vectors of human malaria in the Americas: occurrence data, distribution maps and bionomic précis
inferredcites →https://doi.org/10.1186/1756-3305-4-89openalex-snapshot
The dominant Anopheles vectors of human malaria in the Asia-Pacific region: occurrence data, distribution maps and bionomic précis
inferredcites →https://doi.org/10.1186/1756-3305-5-154openalex-snapshot
Severe Plasmodium vivax malaria among sudanese children at New Halfa Hospital, Eastern Sudan
inferredcites →https://doi.org/10.1186/preaccept-1460941234140079openalex-snapshot
Mortality attributable to Plasmodium vivax malaria: a clinical audit from Papua, Indonesia
inferredcites →https://doi.org/10.1186/s12916-015-0384-6openalex-snapshot
Malaria eradication and elimination: views on how to translate a vision into reality
inferredcites →https://doi.org/10.1186/s12916-015-0491-4openalex-snapshot
Integrating vector control across diseases
inferredcites →https://doi.org/10.1186/s12916-015-0535-9openalex-snapshot
Randomized trial of primaquine hypnozoitocidal efficacy when administered with artemisinin-combined blood schizontocides for radical cure of Plasmodium vivax in Indonesia
inferredcites →https://doi.org/10.1186/s12936-015-0706-3openalex-snapshot
Defining the relationship between Plasmodium vivax parasite rate and clinical disease
inferredcites →https://doi.org/10.1186/s12936-015-0884-zopenalex-snapshot
A systematic review of sub-microscopic Plasmodium vivax infection
inferredcites →https://doi.org/10.1186/s12936-015-0906-xopenalex-snapshot
The epidemiology of subclinical malaria infections in South-East Asia: findings from cross-sectional surveys in Thailand–Myanmar border areas, Cambodia, and Vietnam
inferredcites →https://doi.org/10.1186/s12936-016-1104-1openalex-snapshot
Plasmodium vivax gametocyte infectivity in sub-microscopic infections
inferredcites →https://doi.org/10.1371/journal.pmed.0050127openalex-snapshot
Plasmodium vivax and Mixed Infections Are Associated with Severe Malaria in Children: A Prospective Cohort Study from Papua New Guinea
inferredcites →https://doi.org/10.1371/journal.pmed.0050128openalex-snapshot
Multidrug-Resistant Plasmodium vivax Associated with Severe and Fatal Malaria: A Prospective Study in Papua, Indonesia
inferredcites →https://doi.org/10.1371/journal.pmed.1000283openalex-snapshot
The Impact of Phenotypic and Genotypic G6PD Deficiency on Risk of Plasmodium vivax Infection: A Case-Control Study amongst Afghan Refugees in Pakistan
inferredcites →https://doi.org/10.1371/journal.pmed.1000290openalex-snapshot
Estimating the Global Clinical Burden of Plasmodium falciparum Malaria in 2007
inferredcites →https://doi.org/10.1371/journal.pmed.1001142openalex-snapshot
Worldwide Incidence of Malaria in 2009: Estimates, Time Trends, and a Critique of Methods
inferredcites →https://doi.org/10.1371/journal.pmed.1001195openalex-snapshot
Intermittent Preventive Treatment for Malaria in Papua New Guinean Infants Exposed to Plasmodium falciparum and P. vivax: A Randomized Controlled Trial
inferredcites →https://doi.org/10.1371/journal.pmed.1001305openalex-snapshot
Reduced Risk of Plasmodium vivax Malaria in Papua New Guinean Children with Southeast Asian Ovalocytosis in Two Cohorts and a Case-Control Study
inferredcites →https://doi.org/10.1371/journal.pmed.1001575openalex-snapshot
Major Burden of Severe Anemia from Non-Falciparum Malaria Species in Southern Papua: A Hospital-Based Surveillance Study
inferredcites →https://doi.org/10.1371/journal.pntd.0000774openalex-snapshot
The International Limits and Population at Risk of Plasmodium vivax Transmission in 2009
inferredcites →https://doi.org/10.1371/journal.pntd.0000887openalex-snapshot
Complex Interactions between Soil-Transmitted Helminths and Malaria in Pregnant Women on the Thai-Burmese Border
inferredcites →https://doi.org/10.1371/journal.pntd.0001424openalex-snapshot
Multiplicity and Diversity of Plasmodium vivax Infections in a Highly Endemic Region in Papua New Guinea
inferredcites →https://doi.org/10.1371/journal.pntd.0001814openalex-snapshot
A Long Neglected World Malaria Map: Plasmodium vivax Endemicity in 2010
inferredcites →https://doi.org/10.1371/journal.pntd.0001934openalex-snapshot
Spleen Rupture in a Case of Untreated Plasmodium vivax Infection
inferredcites →https://doi.org/10.1371/journal.pntd.0002403openalex-snapshot
A High Force of Plasmodium vivax Blood-Stage Infection Drives the Rapid Acquisition of Immunity in Papua New Guinean Children
inferredcites →https://doi.org/10.1371/journal.pntd.0003109openalex-snapshot
Epidemiology of Disappearing Plasmodium vivax Malaria: A Case Study in Rural Amazonia
inferredcites →https://doi.org/10.1371/journal.pntd.0003413openalex-snapshot
Systematic Review of Sub-microscopic P. vivax Infections: Prevalence and Determining Factors
inferredcites →https://doi.org/10.1371/journal.pntd.0003758openalex-snapshot
High Rates of Asymptomatic, Sub-microscopic Plasmodium vivax Infection and Disappearing Plasmodium falciparum Malaria in an Area of Low Transmission in Solomon Islands
inferredcites →https://doi.org/10.1371/journal.pntd.0004222openalex-snapshot
Plasmodium vivax Transmission in Africa
inferredcites →https://doi.org/10.1371/journal.pone.0009245openalex-snapshot
The Dynamics of Transmission and Spatial Distribution of Malaria in Riverside Areas of Porto Velho, Rondônia, in the Amazon Region of Brazil
inferredcites →https://doi.org/10.1371/journal.pone.0011206openalex-snapshot
Concurrent Helminthic Infection Protects Schoolchildren with Plasmodium vivax from Anemia
inferredcites →https://doi.org/10.1371/journal.pone.0035406openalex-snapshot
Risk Factors and Characterization of Plasmodium Vivax-Associated Admissions to Pediatric Intensive Care Units in the Brazilian Amazon
inferredcites →https://doi.org/10.1590/s0074-02762006000300001openalex-snapshot
A new challenge for malaria control in Brazil: asymptomatic Plasmodium infection - a review
inferredcites →https://doi.org/10.1603/0022-2585(2005)042[0777:acopsa]2.0.co;2openalex-snapshot
Asymptomatic Carriers of Plasmodium spp. as Infection Source for Malaria Vector Mosquitoes in the Brazilian Amazon
inferredcites →https://doi.org/10.1603/0022-2585-40.4.379openalex-snapshot
Malaria Vectors, Epidemiology, and the Re-Emergence ofAnopheles darlingiin Belém, Pará, Brazil
inferredcites →https://doi.org/10.1645/ge-911r.1openalex-snapshot
GAMETOCYTEMIA IN PLASMODIUM VIVAX AND PLASMODIUM FALCIPARUM INFECTIONS
inferredcites →https://doi.org/10.3201/eid1211.060341openalex-snapshot
Concurrent Plasmodium vivax Malaria and Dengue
inferredcites →https://doi.org/10.3201/eid1307.061386openalex-snapshot
Chloroquine-ResistantPlasmodiumvivax, Brazilian Amazon
inferredcites →https://doi.org/10.3201/eid1504.080891openalex-snapshot
Concurrent Dengue and Malaria in Cayenne Hospital, French Guiana
inferredcites →https://doi.org/10.3201/eid2201.151305openalex-snapshot
FallingPlasmodium knowlesiMalaria Death Rate among Adults despite Rising Incidence, Sabah, Malaysia, 2010–2014
inferredcites →https://doi.org/10.4269/ajtmh.12-0610openalex-snapshot
Plasmodium vivax Hospitalizations in a Monoendemic Malaria Region: Severe Vivax Malaria?
inferredcites →https://doi.org/10.4269/ajtmh.16-0163openalex-snapshot
Epidemiology of Plasmodium vivax Malaria in India
inferredcites →https://doi.org/10.4269/ajtmh.16-0171openalex-snapshot
Diagnosis and Treatment of Plasmodium vivax Malaria
inferredcites →https://doi.org/10.4269/ajtmh.16-0180openalex-snapshot
Key Knowledge Gaps for Plasmodium vivax Control and Elimination
inferredcites →https://doi.org/10.4269/ajtmh.1997.56.621openalex-snapshot
Diagnosis of Resistance to Chloroquine by Plasmodium vivax: Timing of Recurrence and Whole Blood Chloroquine Levels
inferredcites →https://doi.org/10.4269/ajtmh.2001.64.97openalex-snapshot
The neglected burden of Plasmodium vivax malaria
inferredcites →https://doi.org/10.4269/ajtmh.2002.66.641openalex-snapshot
High prevalence of asymptomatic Plasmodium vivax and Plasmodium falciparum infections in native Amazonian populations.
inferredcites →https://doi.org/10.4269/ajtmh.2002.67.141openalex-snapshot
Comparison of field and expert laboratory microscopy for active surveillance for asymptomatic Plasmodium falciparum and Plasmodium vivax in western Thailand.
inferredcites →https://doi.org/10.4269/ajtmh.2003.68.416openalex-snapshot
VERY HIGH RISK OF THERAPEUTIC FAILURE WITH CHLOROQUINE FOR UNCOMPLICATED PLASMODIUM FALCIPARUM AND P. VIVAX MALARIA IN INDONESIAN PAPUA
inferredcites →https://doi.org/10.4269/ajtmh.2006.74.755openalex-snapshot
PREGNANCY OUTCOMES ASSOCIATED WITH PLASMODIUM VIVAX MALARIA IN NORTHEASTERN VENEZUELA
inferredcites →https://doi.org/10.4269/ajtmh.2007.76.997openalex-snapshot
THE RISK OF MALARIAL INFECTIONS AND DISEASE IN PAPUA NEW GUINEAN CHILDREN
inferredcites →https://doi.org/10.4269/ajtmh.2007.77.79openalex-snapshot
Vivax Malaria: Neglected and Not Benign
inferredcites →https://doi.org/10.4269/ajtmh.2007.77.984openalex-snapshot
Demographic Risk Factors for Severe and Fatal Vivax and Falciparum Malaria Among Hospital Admissions in Northeastern Indonesian Papua
inferredcites →https://doi.org/10.4269/ajtmh.2009.80.194openalex-snapshot
Severe Plasmodium vivax Malaria: A Report on Serial Cases from Bikaner in Northwestern India
inferredcites →https://doi.org/10.4269/ajtmh.2009.81.338openalex-snapshot
Resistance to Chloroquine by Plasmodium vivax at Alor in the Lesser Sundas Archipelago in Eastern Indonesia
inferredcites →https://doi.org/10.4269/ajtmh.2010.09-0633openalex-snapshot
Clinical Features of Children Hospitalized with Malaria—A Study from Bikaner, Northwest India
inferredcites →https://doi.org/10.4269/ajtmh.2012.12-0210openalex-snapshot
Clinical Profile of Concurrent Dengue Fever and Plasmodium vivax Malaria in the Brazilian Amazon: Case Series of 11 Hospitalized Patients
inferredcites →https://doi.org/10.4303/jnp/235547openalex-snapshot
The Impact of HIV Coinfection on Cerebral Malaria Pathogenesis
inferredcites →https://doi.org/10.7326/0003-4819-73-4-674_2openalex-snapshot
A Textbook of Malaria Eradication.
inferredcites →https://doi.org/10.7554/elife.04692openalex-snapshot
Modelling the contribution of the hypnozoite reservoir to Plasmodium vivax transmission
inferredcites →https://doi.org/10.7883/yoken.jjid.2006.211openalex-snapshot
Dual Infection by Dengue Virus and Plasmodium vivax in Alappuzha District, Kerala, India
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Association of Impaired Cytochrome P450 2D6 Activity Genotype and Phenotype With Therapeutic Efficacy of Primaquine Treatment for LatentPlasmodium vivaxMalaria
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Primaquine at alternative dosing schedules for preventing relapse in people withPlasmodium vivaxmalaria
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Primaquine alternative dosing schedules for preventing malaria relapse in people withPlasmodium vivax
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Evolutionary pressures and codon bias in low complexity regions of plasmodia
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inferred← citeshttps://doi.org/10.1016/j.ijmm.2017.09.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijpddr.2017.03.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijpp.2023.01.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijregi.2025.100822openalex-snapshot
Plasmodium vivax elimination from India may need therapeutic efficacy studies - Informed shift to artemisinin-based treatment
inferred← citeshttps://doi.org/10.1016/j.imu.2020.100471openalex-snapshot
Exploring novel therapeutic strategies against vivax malaria through an integrated computational investigation to inhibit the merozoite surface protein−1 of Plasmodium vivax
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114384openalex-snapshot
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Validation of a Semiquantitative Real-Time PCR Assay for Malaria Diagnosis and Treatment Monitoring
inferred← citeshttps://doi.org/10.1016/j.jprot.2020.103719openalex-snapshot
Inferring Plasmodium vivax protein biology by using omics data
inferred← citeshttps://doi.org/10.1016/j.jprot.2020.104002openalex-snapshot
A novel platform for peptide-mediated affinity capture and LC-MS/MS identification of host receptors involved in Plasmodium invasion
inferred← citeshttps://doi.org/10.1016/j.jtbi.2022.111014openalex-snapshot
Hypnozoite dynamics for Plasmodium vivax malaria: The epidemiological effects of radical cure
inferred← citeshttps://doi.org/10.1016/j.lana.2022.100420openalex-snapshot
Population-based genomic study of Plasmodium vivax malaria in seven Brazilian states and across South America
inferred← citeshttps://doi.org/10.1016/j.lanwpc.2026.101966openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.meegid.2018.02.018openalex-snapshot
Genetic diversity of the Plasmodium vivax phosphatidylinositol 3-kinase gene in two regions of the China-Myanmar border
inferred← citeshttps://doi.org/10.1016/j.meegid.2019.104161openalex-snapshot
Use of molecular markers can help to understand the genetic diversity of Babesia bovis
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104530openalex-snapshot
Allelic variation of msp-3α gene in Plasmodium vivax isolates and its correlation with the severity of disease in vivax malaria
inferred← citeshttps://doi.org/10.1016/j.meegid.2021.104710openalex-snapshot
Restricted genetic heterogeneity of the Plasmodium vivax transmission-blocking vaccine (TBV) candidate Pvs48/45 in a low transmission setting: Implications for the Plasmodium vivax malaria vaccine development
inferred← citeshttps://doi.org/10.1016/j.meegid.2022.105387openalex-snapshot
PvMSP-3α and PvMSP-3β genotyping reveals higher genetic diversity in Plasmodium vivax parasites from migrant workers than residents at the China-Myanmar border
inferred← citeshttps://doi.org/10.1016/j.microb.2024.100209openalex-snapshot
Epidemiology of Plasmodium vivax malaria infection in Colombia
inferred← citeshttps://doi.org/10.1016/j.omtn.2025.102645openalex-snapshot
mRNA-LNP vaccine encoding the Plasmodium vivax circumsporozoite protein is highly immunogenic and confers protection in mice
inferred← citeshttps://doi.org/10.1016/j.parepi.2020.e00191openalex-snapshot
Temporal trends of gestational malaria in the United States
inferred← citeshttps://doi.org/10.1016/j.parepi.2021.e00203openalex-snapshot
Liver and kidney dysfunction, hypoglycemia, and thrombocytopenia in Plasmodium vivax malaria patients at a Colombian Northwest region
inferred← citeshttps://doi.org/10.1016/j.parepi.2026.e00484openalex-snapshot
Efficacy of primaquine-chloroquine combination on Plasmodium vivax transmission and parasite clearance in Ethiopia: a randomized controlled trial
inferred← citeshttps://doi.org/10.1016/j.parint.2021.102492openalex-snapshot
Serology for Plasmodium vivax surveillance: A novel approach to accelerate towards elimination
inferred← citeshttps://doi.org/10.1016/j.parint.2021.102526openalex-snapshot
Plasmodium vivax – How hidden reservoirs hinder global malaria elimination
inferred← citeshttps://doi.org/10.1016/j.parint.2021.102527openalex-snapshot
Cryptic erythrocytic infections in Plasmodium vivax, another challenge to its elimination
inferred← citeshttps://doi.org/10.1016/j.parint.2022.102592openalex-snapshot
Potential role of vaccines in elimination of Plasmodium vivax
inferred← citeshttps://doi.org/10.1016/j.pt.2019.12.007openalex-snapshot
Single cell sequencing shines a light on malaria parasite relatedness in complex infections
inferred← citeshttps://doi.org/10.1016/j.pt.2020.03.009openalex-snapshot
Plasmodium vivax in the Era of the Shrinking P. falciparum Map
inferred← citeshttps://doi.org/10.1016/j.redox.2018.04.011openalex-snapshot
Integrative metabolomics and transcriptomics signatures of clinical tolerance to Plasmodium vivax reveal activation of innate cell immunity and T cell signaling
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.01.300openalex-snapshot
Projecting potential spatial and temporal changes in the distribution of Plasmodium vivax and Plasmodium falciparum malaria in China with climate change
inferred← citeshttps://doi.org/10.1016/j.scp.2020.100339openalex-snapshot
Malaria vector control strategies. What is appropriate towards sustainable global eradication?
inferred← citeshttps://doi.org/10.1016/j.tmaid.2019.101499openalex-snapshot
Efficacy of directly-observed chloroquine-primaquine treatment for uncomplicated acute Plasmodium vivax malaria in northeast Myanmar: A prospective open-label efficacy trial
inferred← citeshttps://doi.org/10.1016/j.tmaid.2020.101576openalex-snapshot
Single dose tafenoquine for preventing relapse in people with plasmodium vivax malaria-an updated meta-analysis
inferred← citeshttps://doi.org/10.1016/j.tmaid.2021.102251openalex-snapshot
Imported malaria in Switzerland, (1990–2019): A retrospective analysis
inferred← citeshttps://doi.org/10.1016/j.vaccine.2020.02.011openalex-snapshot
Evaluation of Plasmodium vivax HAP2 as a transmission-blocking vaccine candidate
inferred← citeshttps://doi.org/10.1016/j.vaccine.2025.127971openalex-snapshot
Value profile for Malaria vaccines and monoclonal antibodies
inferred← citeshttps://doi.org/10.1016/j.vaccine.2026.128279openalex-snapshot
Immunological response of using emulsifying elongation factor 1 alpha of Plasmodium falciparum-based vaccines in complete Freund's adjuvant
inferred← citeshttps://doi.org/10.1016/s0140-6736(19)31605-8openalex-snapshot
A shorter course for anti-relapse therapy against vivax malaria
inferred← citeshttps://doi.org/10.1016/s1245-1789(19)42011-8openalex-snapshot
Quimioprofilaxis del paludismo
inferred← citeshttps://doi.org/10.1016/s1473-3099(18)30413-4openalex-snapshot
Improving Plasmodium vivax malaria treatment: a little more chloroquine
inferred← citeshttps://doi.org/10.1016/s1473-3099(26)00139-8openalex-snapshot
Dihydroartemisinin–piperaquine versus chloroquine for the treatment of uncomplicated Plasmodium vivax malaria with concurrent or delayed high-dose primaquine in Brazil (Curavivax): an open-label, single-centre, randomised clinical trial
inferred← citeshttps://doi.org/10.1016/s1637-5017(18)79512-4openalex-snapshot
10.1016/s1637-5017(18)79512-4
inferred← citeshttps://doi.org/10.1016/s2352-4642(20)30099-7openalex-snapshot
Deleterious effects of malaria in pregnancy on the developing fetus: a review on prevention and treatment with antimalarial drugs
inferred← citeshttps://doi.org/10.1016/s2352-4642(21)00328-xopenalex-snapshot
Tafenoquine exposure assessment, safety, and relapse prevention efficacy in children with Plasmodium vivax malaria: open-label, single-arm, non-comparative, multicentre, pharmacokinetic bridging, phase 2 trial
inferred← citeshttps://doi.org/10.1016/s2542-5196(24)00021-4openalex-snapshot
Interconnecting global threats: climate change, biodiversity loss, and infectious diseases
inferred← citeshttps://doi.org/10.1016/s2666-5247(22)00118-5openalex-snapshot
Antimalarial drug resistance—is it time to re-evaluate Plasmodium falciparum orthologous genes?
inferred← citeshttps://doi.org/10.1017/s0031182020001596openalex-snapshot
30 years of parasitology research analysed by text mining
inferred← citeshttps://doi.org/10.1017/s0950268823001632openalex-snapshot
Genetic diversity of Plasmodium vivax among immigrant patients exhibiting severe and non-severe clinical manifestations in northern suburbs of Paris
inferred← citeshttps://doi.org/10.1038/s41467-018-03342-5openalex-snapshot
Strong selection during the last millennium for African ancestry in the admixed population of Madagascar
inferred← citeshttps://doi.org/10.1038/s41467-019-08312-zopenalex-snapshot
Plasmodium vivax transcriptomes reveal stage-specific chloroquine response and differential regulation of male and female gametocytes
inferred← citeshttps://doi.org/10.1038/s41467-019-13412-xopenalex-snapshot
Resolving the cause of recurrent Plasmodium vivax malaria probabilistically
inferred← citeshttps://doi.org/10.1038/s41467-021-21886-xopenalex-snapshot
Plasmodium vivax infection compromises reticulocyte stability
inferred← citeshttps://doi.org/10.1038/s41467-024-51949-8openalex-snapshot
Single-cell analyses of polyclonal Plasmodium vivax infections and their consequences on parasite transmission
inferred← citeshttps://doi.org/10.1038/s41467-025-62680-3openalex-snapshot
Worldwide genetic diversity of Plasmodium vivax Pv47 is consistent with natural selection by anopheline mosquitoes
inferred← citeshttps://doi.org/10.1038/s41467-026-68927-xopenalex-snapshot
Variation in pathogen load and the pathogen load–infectiousness relationship broaden avian malaria’s distribution
inferred← citeshttps://doi.org/10.1038/s41467-026-73666-0openalex-snapshot
Two Plasmodium vivax hypnozoite-expressed RNA-binding proteins inhibit liver stage replication
inferred← citeshttps://doi.org/10.1038/s41541-018-0083-3openalex-snapshot
Malaria vaccine candidate based on Duffy-binding protein elicits strain transcending functional antibodies in a Phase I trial
inferred← citeshttps://doi.org/10.1038/s41581-022-00558-zopenalex-snapshot
Kidney complications of parasitic diseases
inferred← citeshttps://doi.org/10.1038/s41598-017-10025-6openalex-snapshot
Plasmodium vivax ligand-receptor interaction: PvAMA-1 domain I contains the minimal regions for specific interaction with CD71+ reticulocytes
inferred← citeshttps://doi.org/10.1038/s41598-018-28757-4openalex-snapshot
Targeting a Reticulocyte Binding Protein and Duffy Binding Protein to Inhibit Reticulocyte Invasion by Plasmodium vivax
inferred← citeshttps://doi.org/10.1038/s41598-018-30713-1openalex-snapshot
Unraveling the Plasmodium vivax sporozoite transcriptional journey from mosquito vector to human host
inferred← citeshttps://doi.org/10.1038/s41598-019-45228-6openalex-snapshot
Complement Receptor 1 availability on red blood cell surface modulates Plasmodium vivax invasion of human reticulocytes
inferred← citeshttps://doi.org/10.1038/s41598-019-51564-4openalex-snapshot
Malaria risk assessment and mapping using satellite imagery and boosted regression trees in the Peruvian Amazon
inferred← citeshttps://doi.org/10.1038/s41598-020-63896-7openalex-snapshot
A spatio-temporal analysis to identify the drivers of malaria transmission in Bhutan
inferred← citeshttps://doi.org/10.1038/s41598-020-78691-7openalex-snapshot
Misidentification of Plasmodium ovale as Plasmodium vivax malaria by a microscopic method: a meta-analysis of confirmed P. ovale cases
inferred← citeshttps://doi.org/10.1038/s41598-021-82928-4openalex-snapshot
Immunoglobulin G responses to variant forms of Plasmodium vivax merozoite surface protein 9 upon natural infection in Thailand
inferred← citeshttps://doi.org/10.1038/s41598-021-93734-3openalex-snapshot
A retrospective analysis of malaria epidemiological characteristics in Yingjiang County on the China–Myanmar border
inferred← citeshttps://doi.org/10.1038/s41598-025-28797-7openalex-snapshot
Highly conserved Plasmodium vivax genomes in Duffy-negative individuals from Sudan
inferred← citeshttps://doi.org/10.1038/s44528-026-00007-4openalex-snapshot
Integrating parallel Plasmodium falciparum and Plasmodium vivax malaria models in a unified framework to capture co-endemic prevalence patterns
inferred← citeshttps://doi.org/10.1051/parasite/2017028openalex-snapshot
An outbreak of locally acquired Plasmodium vivax malaria among migrant workers in Oman
inferred← citeshttps://doi.org/10.1056/nejmc1902327openalex-snapshot
Tafenoquine versus Primaquine to Prevent Relapse of Plasmodium vivax Malaria
inferred← citeshttps://doi.org/10.1056/nejmoa1710775openalex-snapshot
Single-Dose Tafenoquine to Prevent Relapse of Plasmodium vivax Malaria
inferred← citeshttps://doi.org/10.1056/nejmoa1802537openalex-snapshot
Tafenoquine versus Primaquine to Prevent Relapse of Plasmodium vivax Malaria
inferred← citeshttps://doi.org/10.1073/pnas.1920596117openalex-snapshot
Plasmodium vivax spleen-dependent genes encode antigens associated with cytoadhesion and clinical protection
inferred← citeshttps://doi.org/10.1073/pnas.2210181120openalex-snapshot
AIM2 sensors mediate immunity to Plasmodium infection in hepatocytes
inferred← citeshttps://doi.org/10.1073/pnas.2316304121openalex-snapshot
Complement receptor 1 is the human erythrocyte receptor for Plasmodium vivax erythrocyte binding protein
inferred← citeshttps://doi.org/10.1074/jbc.m117.781294openalex-snapshot
CD36 receptor regulates malaria-induced immune responses primarily at early blood stage infection contributing to parasitemia control and resistance to mortality
inferred← citeshttps://doi.org/10.1080/1120009x.2019.1665874openalex-snapshot
Cost-utility of tafenoquine vs. primaquine for the radical cure (prevention of relapse) of Plasmodium vivax malaria
inferred← citeshttps://doi.org/10.1080/13543776.2023.2280596openalex-snapshot
Recent advances on patents of Plasmodium falciparum dihydroorotate dehydrogenase ( Pf DHODH) inhibitors as antimalarial agents
inferred← citeshttps://doi.org/10.1080/21505594.2020.1773107openalex-snapshot
Clinical and epidemiological characterization of severe Plasmodium vivax malaria in Gujarat, India
inferred← citeshttps://doi.org/10.1088/1755-1315/125/1/012098openalex-snapshot
Therapeutic principles of primaquine against relapse ofPlasmodium vivaxmalaria
inferred← citeshttps://doi.org/10.1093/cid/ciab610openalex-snapshot
Relapse of Plasmodium vivax and Plasmodium ovale Malaria With and Without Primaquine Treatment in a Nonendemic Area
inferred← citeshttps://doi.org/10.1093/cid/ciy405openalex-snapshot
Effect of Antiretroviral Therapy on Plasma Concentrations of Chloroquine and Desethyl-chloroquine
inferred← citeshttps://doi.org/10.1093/femsre/fuab047openalex-snapshot
A population genetic perspective on the origin, spread and adaptation of the human malaria agents Plasmodium falciparum and Plasmodium vivax
inferred← citeshttps://doi.org/10.1093/infdis/jiaa287openalex-snapshot
Antimalarial Activity of Artefenomel Against Asexual Parasites and Transmissible Gametocytes During Experimental Blood-Stage Plasmodium vivax Infection
inferred← citeshttps://doi.org/10.1093/infdis/jiag164openalex-snapshot
Predicting Risk of Plasmodium Vivax Microscopy-Detected Episodes Using Serological Markers in Patients With Plasmodium falciparum Malaria: A Multicountry Diagnostic Performance Evaluation
inferred← citeshttps://doi.org/10.1093/infdis/jiag434openalex-snapshot
Temporal Changes in the Genetic Diversity and Relatedness of Plasmodium vivax Clinical Infections in Eastern Cambodia
inferred← citeshttps://doi.org/10.1093/infdis/jiz126openalex-snapshot
Efficacy of Primaquine in Preventing Short- and Long-Latency Plasmodium vivax Relapses in Nepal
inferred← citeshttps://doi.org/10.1093/molbev/msz264openalex-snapshot
Plasmodium vivax Malaria Viewed through the Lens of an Eradicated European Strain
inferred← citeshttps://doi.org/10.1093/ofid/ofag293openalex-snapshot
An Increase in Imported Plasmodium vivax Malaria in New York City: Clinical and Demographic Trends Following Recent Migration
inferred← citeshttps://doi.org/10.1093/trstmh/traa042openalex-snapshot
Case report: recurrence of Plasmodium vivax malaria due to defective cytochrome P450 2D6 function in Pos Lenjang, Pahang, Malaysia
inferred← citeshttps://doi.org/10.1097/fpc.0000000000000407openalex-snapshot
Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria
inferred← citeshttps://doi.org/10.1098/rsob.200180openalex-snapshot
Global distribution of single amino acid polymorphisms in Plasmodium vivax Duffy-binding-like domain and implications for vaccine development efforts
inferred← citeshttps://doi.org/10.1098/rspb.2024.2061openalex-snapshot
Heterogeneous mosquito exposure increases Plasmodium vivax and Plasmodium falciparum co-infections: a modelling study
inferred← citeshttps://doi.org/10.1099/acmi.0.000461.v3openalex-snapshot
A case of atypical vivax malaria with a global review of reports on myriads of morpho-variations in parasitized red blood cells
inferred← citeshttps://doi.org/10.1101/175018openalex-snapshot
Transmission Expression Signature in Nascent Plasmodium vivax Blood Stage Infection
inferred← citeshttps://doi.org/10.1101/2020.03.14.992107openalex-snapshot
Evolutionary Pressures and Codon Bias in Low Complexity Regions of Plasmodia Parasites
inferred← citeshttps://doi.org/10.1101/2021.05.28.446219openalex-snapshot
Differential transcriptomic response of Anopheles arabiensis to Plasmodium vivax and Plasmodium falciparum infection
inferred← citeshttps://doi.org/10.1101/2022.06.07.22275625openalex-snapshot
Non-falciparum malaria infections are as prevalent as P. falciparum among Tanzanian schoolchildren
inferred← citeshttps://doi.org/10.1101/501957openalex-snapshot
Profiling gene expression of the host response to a Plasmodium vivax irradiated sporozoite immunization and infectious challenge
inferred← citeshttps://doi.org/10.1101/505594openalex-snapshot
Estimating the probable cause of recurrence in Plasmodium vivax malaria: relapse, reinfection or recrudescence?
inferred← citeshttps://doi.org/10.1101/508481openalex-snapshot
Duffy Antigen Expression in Erythroid Bone Marrow Precursor Cells of Genotypically Duffy Negative Individuals
inferred← citeshttps://doi.org/10.1108/cc-06-2020-0018openalex-snapshot
The 100 most-cited articles on malaria: a bibliometric analysis
inferred← citeshttps://doi.org/10.1111/cmi.12835openalex-snapshot
Receptor-ligand and parasite protein-protein interactions inPlasmodium vivax: Analysing rhoptry neck proteins 2 and 4
inferred← citeshttps://doi.org/10.1111/mve.70042openalex-snapshot
Chronology of Dichlorodiphenyltrichloroethane and pyrethroid resistance and the associated mutations in Anopheles stephensi : Insights from areas where the vector is native and invasive
inferred← citeshttps://doi.org/10.1111/pim.12580openalex-snapshot
Vivax infection alters peripheral B‐cell profile and induces persistent serum IgM
inferred← citeshttps://doi.org/10.1111/pim.12594openalex-snapshot
Exposure to Plasmodium vivax is associated with the increased expression of exhaustion markers on γδ T lymphocytes
inferred← citeshttps://doi.org/10.1111/tmi.70083openalex-snapshot
Genetic Determinants for Vivax Malaria Susceptibility in Chiplun (Ratnagiri), Maharashtra, India: A Case–Control Study
inferred← citeshttps://doi.org/10.11144/javeriana.10554.38772openalex-snapshot
Estudio de la interacción entre RONs-AMAl de Plasmodium vivax y su capacidad de unión a receptores sobre la célula hospedera
inferred← citeshttps://doi.org/10.1126/sciadv.abc3713openalex-snapshot
Population genomic evidence of Plasmodium vivax Southeast Asian origin
inferred← citeshttps://doi.org/10.1128/aac.00044-24openalex-snapshot
Therapeutic efficacy of pyronaridine-artesunate (Pyramax) in treating Plasmodium vivax malaria in the central highlands of Vietnam
inferred← citeshttps://doi.org/10.1128/aac.00095-21openalex-snapshot
High Proportion of Genome-Wide Homology and Increased Pretreatment pvcrt Levels in Plasmodium vivax Late Recurrences: a Chloroquine Therapeutic Efficacy Study
inferred← citeshttps://doi.org/10.1128/aac.01797-25openalex-snapshot
Differential impact of Tafenoquine and Primaquine on Plasmodium vivax recurrence: the role of CYP2D6 variants
inferred← citeshttps://doi.org/10.1128/iai.00374-23openalex-snapshot
Transmission-reducing and -enhancing monoclonal antibodies against Plasmodium vivax gamete surface protein Pvs48/45
inferred← citeshttps://doi.org/10.1128/mbio.01888-17openalex-snapshot
Genomic Analyses Reveal the Common Occurrence and Complexity of Plasmodium vivax Relapses in Cambodia
inferred← citeshttps://doi.org/10.1128/mmbr.00025-22openalex-snapshot
Transcending Dimensions in Apicomplexan Research: from Two-Dimensional to Three-Dimensional In Vitro Cultures
inferred← citeshttps://doi.org/10.1136/bmjopen-2022-067103openalex-snapshot
Burden and seasonal distribution of malaria in Ziquala district, Northeast Ethiopia: a 5-year multi-centre retrospective study
inferred← citeshttps://doi.org/10.1142/s0218339020500072openalex-snapshot
INFLUENCE OF ASYMPTOMATIC PEOPLE ON MALARIA TRANSMISSION: A MATHEMATICAL MODEL FOR A LOW-TRANSMISSION AREA CASE
inferred← citeshttps://doi.org/10.1142/s1793524520500242openalex-snapshot
The stationary distribution and stochastic persistence for a class of disease models: Case study of malaria
inferred← citeshttps://doi.org/10.1146/annurev-micro-032421-061155openalex-snapshot
Plasmodium vivax Latent Liver Stage Infection and Relapse: Biological Insights and New Experimental Tools
inferred← citeshttps://doi.org/10.1146/annurev-pathmechdis-012419-032557openalex-snapshot
Unraveling Disease Pathophysiology with Mathematical Modeling
inferred← citeshttps://doi.org/10.1155/2018/9720823openalex-snapshot
Relapsing Malaria: A Case Report of Primaquine Resistance
inferred← citeshttps://doi.org/10.1155/2019/4610498openalex-snapshot
Imported Plasmodium vivax Malaria in the Russian Federation from Western Sub-Saharan Africa
inferred← citeshttps://doi.org/10.1155/2019/8568710openalex-snapshot
Plasmodium vivax Infection in Multiple Family Members in Texas, USA
inferred← citeshttps://doi.org/10.1155/2024/8486021openalex-snapshot
Exploring the Infectious Drug Target Glutathione S-Transferase in Plasmodium falciparum with the Inhibitory Potential of Azadirachta indica Phytocompounds
inferred← citeshttps://doi.org/10.1155/japr/6044433openalex-snapshot
Seasonal Climate Drivers and Immunohematological Profiles of Malaria in Rohingya Refugee Camps, Bangladesh: A 4‐Year Repeated Cross‐Sectional Study
inferred← citeshttps://doi.org/10.11606/t.76.2024.tde-26032024-120918openalex-snapshot
Discovery of brussonol analogs as lead candidates for malaria
inferred← citeshttps://doi.org/10.1172/jci134923openalex-snapshot
A Plasmodium vivax experimental human infection model for evaluating efficacy of interventions
inferred← citeshttps://doi.org/10.1172/jci135794openalex-snapshot
Human Plasmodium vivax mosquito experimental transmission
inferred← citeshttps://doi.org/10.1177/00494755251344650openalex-snapshot
Autochthonous cases of malaria in central Anatolia
inferred← citeshttps://doi.org/10.1177/2049936120941725openalex-snapshot
Vector-borne diseases in pregnancy
inferred← citeshttps://doi.org/10.1182/blood-2017-03-774364openalex-snapshot
DARC extracellular domain remodeling in maturating reticulocytes explains Plasmodium vivax tropism
inferred← citeshttps://doi.org/10.1186/s12864-023-09707-5openalex-snapshot
A new Plasmodium vivax reference genome for South American isolates
inferred← citeshttps://doi.org/10.1186/s12879-020-05086-4openalex-snapshot
Resurgence risk for malaria, and the characterization of a recent outbreak in an Amazonian border area between French Guiana and Brazil
inferred← citeshttps://doi.org/10.1186/s12879-021-05783-8openalex-snapshot
Past eight-year malaria data in Gedeo zone, southern Ethiopia: trend, reporting-quality, spatiotemporal distribution, and association with socio-demographic and meteorological variables
inferred← citeshttps://doi.org/10.1186/s12879-023-08381-yopenalex-snapshot
Ethiopian Plasmodium vivax hypnozoites formation dynamics and their susceptibility to reference antimalarial drugs
inferred← citeshttps://doi.org/10.1186/s12889-023-16507-9openalex-snapshot
Determination of different social groups’ level of knowledge about malaria in a multicultural Amazonian cross-border context
inferred← citeshttps://doi.org/10.1186/s12889-024-19206-1openalex-snapshot
Malaria in under-five children: prevalence and multi-factor analysis of high-risk African countries
inferred← citeshttps://doi.org/10.1186/s12916-025-03902-9openalex-snapshot
Spatiotemporal heterogeneity in malaria transmission across Indonesia: analysis of routine surveillance data 2010–2019
inferred← citeshttps://doi.org/10.1186/s12918-018-0669-4openalex-snapshot
Plasmodium vivax readiness to transmit: implication for malaria eradication
inferred← citeshttps://doi.org/10.1186/s12936-016-1619-5openalex-snapshot
Demographic and clinical profiles of Plasmodium falciparum and Plasmodium vivax patients at a tertiary care centre in southwestern India
inferred← citeshttps://doi.org/10.1186/s12936-017-1687-1openalex-snapshot
Genetic diversity of Plasmodium vivax metacaspase 1 and Plasmodium vivax multi-drug resistance 1 genes of field isolates from Mauritania, Sudan and Oman
inferred← citeshttps://doi.org/10.1186/s12936-017-1925-6openalex-snapshot
Malaria in Brazil, Colombia, Peru and Venezuela: current challenges in malaria control and elimination
inferred← citeshttps://doi.org/10.1186/s12936-017-1931-8openalex-snapshot
Dynamics of Plasmodium vivax sporogony in wild Anopheles stephensi in a malaria-endemic region of Western India
inferred← citeshttps://doi.org/10.1186/s12936-017-1944-3openalex-snapshot
Population-level estimates of the proportion of Plasmodium vivax blood-stage infections attributable to relapses among febrile patients attending Adama Malaria Diagnostic Centre, East Shoa Zone, Oromia, Ethiopia
inferred← citeshttps://doi.org/10.1186/s12936-017-2008-4openalex-snapshot
A model of Plasmodium vivax concealment based on Plasmodium cynomolgi infections in Macaca mulatta
inferred← citeshttps://doi.org/10.1186/s12936-017-2029-zopenalex-snapshot
Integrative analysis associates monocytes with insufficient erythropoiesis during acute Plasmodium cynomolgi malaria in rhesus macaques
inferred← citeshttps://doi.org/10.1186/s12936-017-2031-5openalex-snapshot
Proximity to vector breeding site and risk of Plasmodium vivax infection: a prospective cohort study in rural Ethiopia
inferred← citeshttps://doi.org/10.1186/s12936-017-2090-7openalex-snapshot
Long-term in vitro culture of Plasmodium vivax isolates from Madagascar maintained in Saimiri boliviensis blood
inferred← citeshttps://doi.org/10.1186/s12936-017-2143-yopenalex-snapshot
Are respiratory complications of Plasmodium vivax malaria an underestimated problem?
inferred← citeshttps://doi.org/10.1186/s12936-018-2190-zopenalex-snapshot
Primaquine ineligibility in anti-relapse therapy of Plasmodium vivax malaria: the problem of G6PD deficiency and cytochrome P-450 2D6 polymorphisms
inferred← citeshttps://doi.org/10.1186/s12936-018-2228-2openalex-snapshot
Sudden spleen rupture in a Plasmodium vivax-infected patient undergoing malaria treatment
inferred← citeshttps://doi.org/10.1186/s12936-018-2243-3openalex-snapshot
Asymptomatic Plasmodium vivax parasitaemia in the low-transmission setting: the role for a population-based transmission-blocking vaccine for malaria elimination
inferred← citeshttps://doi.org/10.1186/s12936-018-2337-yopenalex-snapshot
Multiplicity and molecular epidemiology of Plasmodium vivax and Plasmodium falciparum infections in East Africa
inferred← citeshttps://doi.org/10.1186/s12936-018-2560-6openalex-snapshot
Analysis of erythrocyte dynamics in Rhesus macaque monkeys during infection with Plasmodium cynomolgi
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