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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

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In pathological conditions astroglial cells undergo multiple progressive and/or regressive changes, which can to a significant extent determine the progression and outcome of neurological diseases as discussed below