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1 ds (DPPH, ORAC and erythrocyte resistance to haemolysis).
2 rds hydrogen peroxide and on surface-induced haemolysis.
3 altering red blood cell rheology and causing haemolysis.
4 nd no evidence of hepatitis, cholestasis, or haemolysis.
5 c sucrose solutions at pH 6) supported their haemolysis.
6 Cytochalasin B prevented haemolysis.
7 of individuals at risk of primaquine-induced haemolysis.
8 o sustained reticulocytopenia, to near-fatal haemolysis.
9 ver, abnormal liver function tests, and mild haemolysis.
10 ompromised, the RBCs are more susceptible to haemolysis.
12 lation of eight mutants that failed to cause haemolysis, all of which had transposon insertions in ge
13 nillin or 5-hydroxymethyl, and urea) reduced haemolysis, an effect not due to increased oxygen affini
15 ubarachnoid haemorrhage is often followed by haemolysis and concomitant oxidative stress, and is freq
16 nto the mechanism of streptolysin S-mediated haemolysis and have implications for the development of
20 12 patients reported serious adverse events; haemolysis and pyrexia were the most common (each occurr
21 oposed direct link between contact-dependent haemolysis and Shigella entry, and demonstrate that IpaB
22 hildren showed evidence of treatment-related haemolysis, and the mean maximum decrease in haemoglobin
26 may result in a ten-fold increase in sample haemolysis, compared to the recommended guideline proced
28 progressive changes in the profile of their haemolysis curves, as the curves migrated towards lower
29 showed no change in profile of the migrating haemolysis curves, suggesting that their PCl distributio
30 on (2 [6%]), and one (3%) each with anaemia, haemolysis, fatigue, and a neurological, metabolic, resp
31 ched the threshold of clinically significant haemolysis (fractional haematocrit reduction >25%) in G6
37 he potential to cause clinically significant haemolysis in G6PD heterozygous females who are reported
38 primaquine or tafenoquine) is complicated by haemolysis in individuals with glucose-6-phosphate dehyd
41 ial was designed to measure efficacy and not haemolysis in relation to G6PD genotype and that the het
49 that at temperatures < or = 15 degrees C the haemolysis rate was significantly inhibited with little
52 Many acute and chronic anaemias, including haemolysis, sepsis and genetic bone marrow failure disea
55 r [11%] of 37), chest pain (two [5%] of 37), haemolysis (two [5%] of 37), and neutropenia (two [5%] o
56 designed to characterise primaquine-induced haemolysis using a holistic Bayesian analysis of all pub
62 e rate of sample laboratory rejection due to haemolysis when commonly practiced deviations from the g
64 adherence to the vascular endothelium and by haemolysis, which results in endothelial cell activation
65 rent work addresses the hypothesis that this haemolysis will provide a novel diagnostic and prognosti
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