Rapid thin-layer chromatographic method for the detection of urinary methylmalonic acid
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference10 articles.
1. Inborn errors of organic acid metabolism;Gompertz;Clinics in Endocrinology and metabolism,1974
2. Unpublished data.
3. A Rapid Screening Test for the Detection of Congenital Methylmalonic Aciduria in Infancy
4. A simple and rapid thin-layer chromatographic technique for the detection of methylmalonic acid in urine
5. The rapid detection of methylmalonic acid in urine—a sensitive index of vitamin B12 deficiency
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2. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort;Journal of Inherited Metabolic Disease;2019-01
3. An improved method for glycosaminoglycan analysis by LC–MS/MS of urine samples collected on filter paper;Clinica Chimica Acta;2012-04
4. Quebec neonatal mass urinary screening programme: From micromolecules to macromolecules;Journal of Inherited Metabolic Disease;2007-06-14
5. Newborn urine screening experience with over one million infants in the Quebec Network of Genetic Medicine;Journal of Inherited Metabolic Disease;1988-03
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