The Rapid and Sensitive Quantitative Determination of Galactose by Combined Enzymatic and Colorimetric Method: Application in Neonatal Screening
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Published:2016-01-28
Issue:2
Volume:179
Page:283-293
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ISSN:0273-2289
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Container-title:Applied Biochemistry and Biotechnology
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language:en
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Short-container-title:Appl Biochem Biotechnol
Author:
Kianmehr AnvarsadatORCID, Mahrooz Abdolkarim, Ansari Javad, Oladnabi Morteza, Shahbazmohammadi Hamid
Funder
Biochemistry and Metabolic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Applied Microbiology and Biotechnology,Biochemistry,General Medicine,Bioengineering,Biotechnology
Reference21 articles.
1. Berry, G. T. (2012). Galactosemia: when is it a newborn screening emergency? Molecular Genetics and Metabolism, 106, 7–11. 2. Hughes, J., Ryan, S., Lambert, D., Geoghegan, O., Clark, A., Rogers, Y., Hendroff, U., Monavari, A., Twomey, E., & Treacy, E. P. (2009). Outcomes of siblings with classical galactosemia. Journal of Pediatric, 154, 721–726. 3. Doyle, C. M., Channon, S., Orlowska, D., & Lee, P. J. (2010). The neuropsychological profile of galactosaemia. Journal of Inherited Metabolic Diseases, 33, 603–609. 4. Mirzaee, A., Pishva, N., Karamizadeh, Z., Purarian, S., Hemati, F., Razavi, M., Saki, F., Bahrami, R., Bagheri, F., Rastegar, M., & Rahimi, N. (2014). The incidence and clinical study of galactosemia in Fars province in south of Iran. Galen Medical Journal, 3, 39–45. 5. Clague, A., & Thomas, A. (2002). Neonatal biochemical screening for disease. Clinica Chimica Acta, 315, 99–110.
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