Screening for Phenylketonuria

This publication has 11 references indexed in Scilit:

• Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterin
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1979
• Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.
  BMJ, 1978
• In vivo Determination of Phenylalanine Hydroxylase Activity Using Heptadeutero-Phenylalanine and Comparison to the in vitro Assay Values1
  Published by S. Karger AG ,1977
• Termination of dietary treatment in phenylketonuria
  European Journal of Pediatrics, 1977
• Dihydroxanthopterinuria in phenylketonuria and lethal hyperphenylalaninemia patients
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1977
• NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTION
  The Lancet, 1975
• A Simple Chromatographic Screening Test for the Detection of Disorders of Amino Acid Metabolism
  New England Journal of Medicine, 1964
• A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS
  Pediatrics, 1963
• The Influence of Phenylalanine Intake on the Chemistry and Behaviour of a Phenylketonuria Child
  Acta Paediatrica, 1954
• AN ATYPICAL CASE OF PHENYLKETONURIA
  The Lancet, 1951