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Clinical and laboratory features of SCD and non-SCD individuals aged 5–17 years
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Fatal outbreaks are highlighted in light red. Data are separated according to changes in sample preparation affecting levels of PCR product: (A) red blood cell pellets were extracted from all samples collected in 1984–1996, while (B) whole blood was collected for all subsequent samples. The relative quantity of hemoparasite DNA was calculated as average threshold PCR cycle divided by <t>hemoglobin</t> concentration and expressed as the fold difference greater than the sample with the smallest quantity of hemoparasite DNA. Levels of Babesia infection were significantly higher during the fatal outbreaks, in the Crater, and in assays performed on whole blood (all three factors significant at P<0.0001 in a multivariate analysis, n = 344).
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Fatal outbreaks are highlighted in light red. Data are separated according to changes in sample preparation affecting levels of PCR product: (A) red blood cell pellets were extracted from all samples collected in 1984–1996, while (B) whole blood was collected for all subsequent samples. The relative quantity of hemoparasite DNA was calculated as average threshold PCR cycle divided by <t>hemoglobin</t> concentration and expressed as the fold difference greater than the sample with the smallest quantity of hemoparasite DNA. Levels of Babesia infection were significantly higher during the fatal outbreaks, in the Crater, and in assays performed on whole blood (all three factors significant at P<0.0001 in a multivariate analysis, n = 344).
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Image Search Results


Clinical and laboratory features of SCD and non-SCD individuals aged 5–17 years

Journal: BMC Hematology

Article Title: A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania

doi: 10.1186/s12878-018-0125-0

Figure Lengend Snippet: Clinical and laboratory features of SCD and non-SCD individuals aged 5–17 years

Article Snippet: At enrolment visits, peripheral blood samples in EDTA were analyzed for full blood count (haemoglobin (Hb), red blood cell count (RBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin Concentration (MCHC)], white blood cell (WBC) and platelet count (PLT) (Pentra 60, Horiba ABX, Kyoto, Japan; Sysmex XT2000i, Hyogo, Japan).

Techniques: Concentration Assay

Clinical and laboratory features of SCD individuals in 3 age categories (< 5 years; 5–17 years and ≥ 18 years)

Journal: BMC Hematology

Article Title: A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania

doi: 10.1186/s12878-018-0125-0

Figure Lengend Snippet: Clinical and laboratory features of SCD individuals in 3 age categories (< 5 years; 5–17 years and ≥ 18 years)

Article Snippet: At enrolment visits, peripheral blood samples in EDTA were analyzed for full blood count (haemoglobin (Hb), red blood cell count (RBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin Concentration (MCHC)], white blood cell (WBC) and platelet count (PLT) (Pentra 60, Horiba ABX, Kyoto, Japan; Sysmex XT2000i, Hyogo, Japan).

Techniques: Concentration Assay

Fatal outbreaks are highlighted in light red. Data are separated according to changes in sample preparation affecting levels of PCR product: (A) red blood cell pellets were extracted from all samples collected in 1984–1996, while (B) whole blood was collected for all subsequent samples. The relative quantity of hemoparasite DNA was calculated as average threshold PCR cycle divided by hemoglobin concentration and expressed as the fold difference greater than the sample with the smallest quantity of hemoparasite DNA. Levels of Babesia infection were significantly higher during the fatal outbreaks, in the Crater, and in assays performed on whole blood (all three factors significant at P<0.0001 in a multivariate analysis, n = 344).

Journal: PLoS ONE

Article Title: Climate Extremes Promote Fatal Co-Infections during Canine Distemper Epidemics in African Lions

doi: 10.1371/journal.pone.0002545

Figure Lengend Snippet: Fatal outbreaks are highlighted in light red. Data are separated according to changes in sample preparation affecting levels of PCR product: (A) red blood cell pellets were extracted from all samples collected in 1984–1996, while (B) whole blood was collected for all subsequent samples. The relative quantity of hemoparasite DNA was calculated as average threshold PCR cycle divided by hemoglobin concentration and expressed as the fold difference greater than the sample with the smallest quantity of hemoparasite DNA. Levels of Babesia infection were significantly higher during the fatal outbreaks, in the Crater, and in assays performed on whole blood (all three factors significant at P<0.0001 in a multivariate analysis, n = 344).

Article Snippet: Therefore, samples were normalized using hemoglobin concentrations (Pentra 60, Horiba ABX Montpellier, France) as a proxy for RBC number.

Techniques: Sample Prep, Concentration Assay, Infection