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47  Articles
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The aim of this study is to analyze the relationship between the types of G6PD mutations found in Indonesia and the relationships of mutations found in Indonesia to those found in other countries. We summarize the distribution of G6PDs in West Indonesia a... see more

Background: Newborn screening (NBS) for metabolic and genetic disorders, which can be treated or modified if detected early in life, can help to prevent potentially disastrous consequences and save a precious life. However, there is no nationwide consensu... see more

El déficit de glucosa-6-fosfato deshidrogenasa es el defecto enzimático más frecuente de los glóbulos rojos en los seres humanos. Esta alteración está relacionada con un defecto enzimático en la vía de las pentosas-fosfato y cursa con hemólisis. Evitar po... see more

 
We have previously developed the WST-8 method as a simple and rapid screening test for detection of glucose-6-phosphate dehydrogenase (G6PD) deficiency accomplished by the naked eye. However, it was little difficult to distinguish between faint orange col... see more

We have previously developed the WST-8 method as a simple and rapid screening test for detection of glucose-6-phosphate dehydrogenase (G6PD) deficiency accomplished by the naked eye. However, it was little difficult to distinguish between faint orange col... see more

El déficit de glucosa-6-fosfato deshidrogenasa es el defecto enzimático más frecuente de los glóbulos rojos en los seres humanos. Esta alteración está relacionada con un defecto enzimático en la vía de las pentosas-fosfato y cursa con hemólisis. Evitar po... see more

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