Edwin Naylor to Metabolism, Inborn Errors
This is a "connection" page, showing publications Edwin Naylor has written about Metabolism, Inborn Errors.
Connection Strength
0.706
-
Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency. Mol Genet Metab. 2003 Feb; 78(2):100-7.
Score: 0.207
-
Electrospray tandem mass spectrometry for analysis of acylcarnitines in dried postmortem blood specimens collected at autopsy from infants with unexplained cause of death. Clin Chem. 2001; 47(7):1166-82.
Score: 0.179
-
Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millennium. Acta Paediatr Suppl. 1999 Dec; 88(432):45-7.
Score: 0.166
-
Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress. JAMA. 2003 Nov 19; 290(19):2564-72.
Score: 0.055
-
Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism. J Child Neurol. 1999 Nov; 14 Suppl 1:S4-8.
Score: 0.041
-
A simple screening test for arginase deficiency (hyperargininemia). J Lab Clin Med. 1977 Apr; 89(4):876-80.
Score: 0.035
-
Neonatal urine screening for metabolic disease with auxotrophic strains of Bacillus subtilis. Clin Chim Acta. 1982 Mar 12; 119(3):345-9.
Score: 0.012
-
A simple screening test for reduced glutathione in filter paper spots of blood. J Pediatr. 1981 Feb; 98(2):265-7.
Score: 0.011