Usefulness of Benedict's test for the screening of galactosemia
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference14 articles.
1. Newborn screening for galactosemia and other galactose metabolic defects;Levy;J Pediatr,1978
2. Hypotonia and lethargy: initial manifestations of a new case of galactosemia;Vázquez-López;Rev Neurol,2004
3. Clinical significance of plasma galactose and erythrocyte galactose-1-phosphate measurements in transferase-deficient galactosemia and in individuals with below-normal transferase activity;Pesce;Clin Chem,1982
4. Galactosemia: when is it a newborn screening emergency?;Berry;Mol Genet Metab,2012
5. An improved quantitative assay of galactose-1-phosphate uridyltransferase activity in erythrocytes based on the determination of glucose-1-phosphate generation;Shutgens;Clin Chim Acta,1978
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1. Update of a colorimetric method for quantitative determination of galactose in blood samples: A simple and rapid method for the early detection of inherited metabolic diseases;Carbohydrate Research;2020-12
2. Newborn screening for galactosaemia;Cochrane Database of Systematic Reviews;2020-06-22
3. Five years of screening for galactosaemia in South Africa: Pitfalls of using Benedict’s test and thin layer chromatography to screen for galactosaemia in a developing country;Clinica Chimica Acta;2020-06
4. Newborn screening for galactosaemia;Cochrane Database of Systematic Reviews;2017-12-23
5. Newborn screening for galactosaemia;Cochrane Database of Systematic Reviews;2016-07-03
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