16 research outputs found
Sample description for genotyped samples.
a<p>Discordant: Phenotype deficient, but with wild type for the Med- allele. The three discordant females were all homozygous WT against the Med allele assay.</p
Unadjusted ORs and AORs for phenotypic G6PD deficiency stratified by sex.
a<p>Odds ratios adjusted for village (unpublished data); age group and tribe were dropped due to no univariate effect (age group) or low sample sizes (tribe).</p
Characteristics of cases and controls.
a<p>Data missing from four controls.</p>b<p>Chi<sup>2</sup> = 59.5, <i>p</i><0.001.</p
The geographical distribution of studies and patients by country.
<p>The geographical distribution of studies and patients by country.</p
Box plot showing duration of follow-up in VL studies.
<p>The majority of studies (104 studies, 21,070 patients) had a follow-up duration of six months. Two studies (406 patients) had a nine month follow-up duration and 24 studies (4,546 patients) had a one year follow-up duration.</p
The geographical distribution of studies and patients by country.
<p>The geographical distribution of studies and patients by country.</p
Pie chart and table showing the design and method of patient allocation in published visceral leishmaniasis clinical studies.
<p>Pie chart and table showing the design and method of patient allocation in published visceral leishmaniasis clinical studies.</p
The drugs and dose regimens used in visceral leishmaniasis clinical studies.
<p>The drugs and dose regimens used in visceral leishmaniasis clinical studies.</p
The number of visceral leishmaniasis clinical trials identified in searches of clinical trial registries and publication databases.
<p>The number of visceral leishmaniasis clinical trials identified in searches of clinical trial registries and publication databases.</p
Bar chart showing dose regimens used in visceral leishmaniasis clinical studies.
<p>Bars show the number of patients treated with the drug in visceral leishmaniasis clinical studies. Bars are colored according to the dose regimen.</p