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TABLE 2 Comparison of the Two Most Common Variants of G6PD Deficiency Diagnosis The diagnosis of G6PD deficiency is made by a quantitative spectrophotometric analysis or, more commonly, by a rapid fluorescent spot test detecting the generation of NADPH from NADP

[EBV infection revealing a long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency in a 3-year-old boy]

Ito et al., 2018)

Indeed, as the asexual cycle number increases, so does the load of homocysteine levels in the circulation of the malaria patient and consequently the number of gametocytes

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Well, I believe there's always room for improvement