Connection

Edwin Naylor to Male

This is a "connection" page, showing publications Edwin Naylor has written about Male.
Connection Strength

0.102
  1. 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.
    View in: PubMed
    Score: 0.018
  2. Alternative DNA-based newborn screening for glucose-6-phosphate dehydrogenase deficiency. Mol Genet Metab. 2005 Sep-Oct; 86(1-2):212-9.
    View in: PubMed
    Score: 0.013
  3. The use of filter paper-dried blood spots for thyroid-antibody screening in adults. J Lab Clin Med. 2004 Dec; 144(6):307-12.
    View in: PubMed
    Score: 0.013
  4. 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.
    View in: PubMed
    Score: 0.009
  5. Molecular analysis using targeted next generation DNA sequencing and clinical spectrum of Mexican patients with isovaleric acidemia. Clin Chim Acta. 2020 Feb; 501:216-221.
    View in: PubMed
    Score: 0.009
  6. Twenty-year follow-up of newborn screening for patients with muscular dystrophy. Muscle Nerve. 2016 Apr; 53(4):570-8.
    View in: PubMed
    Score: 0.007
  7. Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. Pediatr Res. 1995 May; 37(5):675-8.
    View in: PubMed
    Score: 0.007
  8. Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy. Muscle Nerve. 2014 Jun; 49(6):822-8.
    View in: PubMed
    Score: 0.006
  9. Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. Mol Genet Metab. 2010 Sep; 101(1):33-9.
    View in: PubMed
    Score: 0.005
  10. Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress. JAMA. 2003 Nov 19; 290(19):2564-72.
    View in: PubMed
    Score: 0.003
  11. Neonatal blood carnitine concentrations: normative data by electrospray tandem mass spectometry. Pediatr Res. 2003 May; 53(5):823-9.
    View in: PubMed
    Score: 0.003
  12. DNA microarray technology for neonatal screening. Acta Paediatr Suppl. 1999 Dec; 88(432):61-4.
    View in: PubMed
    Score: 0.002
  13. Immunoreactive trypsinogen levels in pediatric patients with intestinal failure awaiting intestinal transplantation. Clin Transplant. 1999 Oct; 13(5):395-9.
    View in: PubMed
    Score: 0.002
  14. Elevated immunoreactive trypsinogen levels in pediatric patients with short bowel syndrome. Transplant Proc. 1998 Sep; 30(6):2549-50.
    View in: PubMed
    Score: 0.002
  15. 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.
    View in: PubMed
    Score: 0.001
  16. Ultramicromethod for estimation of total glutathione in dried blood spots on filter paper. Anal Biochem. 1980 May 01; 104(1):70-4.
    View in: PubMed
    Score: 0.001
  17. Micromethod for estimating adenosine deaminase activity in dried blood spots on filter paper. Clin Chem. 1978 Apr; 24(4):591-4.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.