Edwin Naylor to Infant
This is a "connection" page, showing publications Edwin Naylor has written about Infant.
Connection Strength
0.153
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A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin. J Hum Genet. 2009 Jun; 54(6):335-9.
Score: 0.052
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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: 0.029
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Direct analysis of filter paper blood specimens for identification of Smith-Lemli-Opitz syndrome using time-of-flight secondary ion mass spectrometry. Am J Med Genet. 1997 Jan 31; 68(3):300-4.
Score: 0.022
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Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. Mol Genet Metab. 2010 Sep; 101(1):33-9.
Score: 0.014
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A rapid screening test for Duchenne muscular dystrophy using dried blood specimens. Clin Chim Acta. 1984 Apr 27; 138(3):267-74.
Score: 0.009
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Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress. JAMA. 2003 Nov 19; 290(19):2564-72.
Score: 0.009
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Immunoreactive trypsinogen levels in pediatric patients with intestinal failure awaiting intestinal transplantation. Clin Transplant. 1999 Oct; 13(5):395-9.
Score: 0.007
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Elevated immunoreactive trypsinogen levels in pediatric patients with short bowel syndrome. Transplant Proc. 1998 Sep; 30(6):2549-50.
Score: 0.006
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Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolism. Am J Hum Genet. 1993 Sep; 53(3):768-74.
Score: 0.004
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Ultramicromethod for estimation of total glutathione in dried blood spots on filter paper. Anal Biochem. 1980 May 01; 104(1):70-4.
Score: 0.002