Logistic models to examine the effect of ITN use and transmission intensity on the category of malaria infection, and their interactions with age.

<p>Odds ratios (OR) from logistic regression are shown, for the risk of febrile malaria compared with asymptomatic infection, and then for the risk of any malaria infection (i.e. asymptomatic infection or febrile malaria) with uninfected status. Children are divided into equal groups of younger (12–42 months) and older (42–80 months) children. The ORs are shown for the effect of ITN use according among the younger and then older children separately, and then the interaction term for ITN use and older age is shown by *. The same format is then used for the effect of residence at low transmission intensity (Low trans.).</p

Survival plot of time to first episode of febrile malaria (>2,500 parasites per µl).

<p>Children are divided by age (in two categories) and by residence (in two transmission zones). P<0.0001 by logrank.</p

The effect of ITN use and residence at low transmission intensity on risk of febrile malaria, and the interactions with age group.

<p>Hazard ratios (HR) from Cox regression and incidence rate ratios (IRR) from Poisson regression are shown for survival and multiple event analyses, respectively. Children are divided into equal groups of younger (12–42 months) and older (42–80 months) children. The interaction term for ITN use and older age is shown by *. (i.e. the HR/IRR for what was observed in older children using ITNs compared with what would have been predicted for the additive effect of ITN use and older age).</p

Survival plot of time to first episode of febrile malaria (>2,500 parasites per µl).

<p>Children are divided by age (in two categories) and by ITN use. P<0.0001 by logrank.</p

The incidence rates of febrile malaria by age and ITN use.

<p>The incidence rates of febrile malaria by age and ITN use.</p

Impact of Treatment with Naloxegol for Opioid-Induced Constipation on Patients’ Health State Utility

<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>. </b><a href="https://link.springer.com/article/10.1007/s12325-016-0365-y">https://link.springer.com/article/10.1007/s12325-016-0365-y</a></p><p></p> <p><br></p> <p><b>Provide enhanced content for this article</b></p> <p><br></p> <p>If you are an author of this publication and would like to provide additional enhanced content for your article then please contact <a href="http://www.medengine.com/Redeem/”mailto:[email protected]”"><b>[email protected]</b></a>.</p> <p><br></p> <p>The journal offers a range of additional features designed to increase visibility and readership. All features will be thoroughly peer reviewed to ensure the content is of the highest scientific standard and all features are marked as ‘peer reviewed’ to ensure readers are aware that the content has been reviewed to the same level as the articles they are being presented alongside. Moreover, all sponsorship and disclosure information is included to provide complete transparency and adherence to good publication practices. This ensures that however the content is reached the reader has a full understanding of its origin. No fees are charged for hosting additional open access content.</p> <p><br></p> <p>Other enhanced features include, but are not limited to:</p> <p><br></p> <p>• Slide decks</p> <p>• Videos and animations</p> <p>• Audio abstracts</p> <p>• Audio slides</p

IgG antibody responses to merozoite antigens in Kenyan children have a short half-life-0

<p><b>Copyright information:</b></p><p>Taken from "IgG antibody responses to merozoite antigens in Kenyan children have a short half-life"</p><p>http://www.malariajournal.com/content/6/1/82</p><p>Malaria Journal 2007;6():82-82.</p><p>Published online 28 Jun 2007</p><p>PMCID:PMC1920526.</p><p></p>d's study number. a) Children who had moderate to high level of antibodies to one or more antigens at presentation to hospital. b) Children who made a distinct responses to one or more antigens after presentation to hospital. For the responses whose half-life was estimated, the sampling points used in the estimation are joined by a bold line. Responses that peaked beyond the interpolation range of the standard curve are plotted in dotted lines. The solid triangles below the plots indicate time points when the children were positive for malaria parasites

Proportions of Variation Explained by Additive Genetics, Household, and Other Factors in the Incidence of Malarial and Nonmalarial Mild (Study 1) and Hospitalised (Study 2) Disease in the Study Populations of Coastal Kenya Using Method 1

<p>Colour coding for all four charts follows that in the top left using method 1.</p

Mean Annual Incidence of Malarial and Nonmalarial Fevers in the Mild (Study 1) and Hospitalised (Study 2) Disease Studies in Coastal Kenya

<p>Mean Annual Incidence of Malarial and Nonmalarial Fevers in the Mild (Study 1) and Hospitalised (Study 2) Disease Studies in Coastal Kenya</p

Multidisciplinary in-depth investigations of head-on and left-turn road collisions

Additional file 3. The proportion of same and different genotype parasite pairs in vivo and in vitro