Phenylketonuria screening using the Quantase phenylalanine kit in combination with a microfilter system and the dye Tartrazine
- 31 March 1995
- Vol. 3 (4) , 209-223
- https://doi.org/10.1016/0925-6164(94)00026-5
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Neonatal Screening for Phenylketonuria: Evaluation of an Automated Enzymatic MethodAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1994
- Evaluation of an enzymatic, colorimetric method for the neonatal screening of phenylketonuriaScreening, 1993
- A method of PKU screening using phenylalanine dehydrogenase and microplate systemScreening, 1992
- Microassay system for newborn screening for phenylketonuria, maple syrup urine disease, homocystinuria, histidinemia and galactosemia with use of a fluorometric microplate readerScreening, 1992
- A new approach to the newborn screening for hyperphenylalaninemias: use of L-phenylalanine dehydrogenase and microtiter platesClinica Chimica Acta; International Journal of Clinical Chemistry, 1990
- Fluorometric method for phenylalanine microplate assay adapted for phenylketonuria screening.Clinical Chemistry, 1989
- EFFECT OF ANTIMICROBIAL AGENTS ON GUTHRIE TEST AND ITS REVERSAL BY AUTOCLAVINGThe Lancet, 1985
- Determination of phenylalanine in filter paper blood spots by a simplified automated fluorimetric method without dialysisClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTSPediatrics, 1963