1,721,173 research outputs found

    Giuseppina LEGROTTAGLIE, Ritratti e statue iconiche di età romana nel Museo civico G. Fiorelli di Lucera.

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    Evers Cécile. Giuseppina LEGROTTAGLIE, Ritratti e statue iconiche di età romana nel Museo civico G. Fiorelli di Lucera.. In: L'antiquité classique, Tome 74, 2005. pp. 638-639

    Pompei. Il Foro Civile nella Pompeianarum Antiquitatum Historia di G. Fiorelli

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    Item does not contain fulltextM. Grimaldi Pompei. Il Foro Civile nella Pompeianarum Antiquitatum Historia di G. Fiorelli Napels:Valtrend ,2015 978888862335

    Giuseppina LEGROTTAGLIE, Ritratti e statue iconiche di età romana nel Museo civico G. Fiorelli di Lucera.

    No full text
    Evers Cécile. Giuseppina LEGROTTAGLIE, Ritratti e statue iconiche di età romana nel Museo civico G. Fiorelli di Lucera.. In: L'antiquité classique, Tome 74, 2005. pp. 638-639

    Glucose-6-phosphate dehydrogenase deficiency

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    Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being present in more than 400 million people worldwide. The global distribution of this disorder is remarkably similar to that of malaria, lending support to the so-called malaria protection hypothesis. G6PD deficiency is an X-linked, hereditary genetic defect due to mutations in the G6PD gene, which cause functional variants with many biochemical and clinical phenotypes. About 140 mutations have been described: most are single base changes, leading to aminoacid substitutions. The most frequent clinical manifestations of G6PD deficiency are neonatal jaundice, and acute haemolytic anaemia, which is usually triggered by an exogenous agent. Some G6PD variants cause chronic haemolysis, leading to congenital non-spherocytic haemolytic anaemia. The most effective management of G6PD deficiency is to prevent haemolysis by avoiding oxidative stress. Screening programmes for the disorder are undertaken, depending on the prevalence of G6PD deficiency in a particular community
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