Journal of Inherited Metabolic Disease

, Volume 23, Issue 4, pp 325–328

Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiency

  • N. G. G. M. Abeling
  • C. Bräutigam
  • G. F. Hoffmann
  • P. G. Barth
  • R. A. Wevers
  • J. Jaeken
  • A. Fiumara
  • A. Knust
  • A. H. van Gennip
Article

DOI: 10.1023/A:1005650325003

Cite this article as:
Abeling, N.G.G.M., Bräutigam, C., Hoffmann, G.F. et al. J Inherit Metab Dis (2000) 23: 325. doi:10.1023/A:1005650325003

Copyright information

© Kluwer Academic Publishers 2000

Authors and Affiliations

  • N. G. G. M. Abeling
    • 1
  • C. Bräutigam
    • 2
  • G. F. Hoffmann
    • 2
  • P. G. Barth
    • 1
  • R. A. Wevers
    • 3
  • J. Jaeken
    • 4
  • A. Fiumara
    • 5
  • A. Knust
    • 6
  • A. H. van Gennip
    • 1
  1. 1.Department of Clinical Chemistry and Division Emma Children's HospitalAcademic Medical Center, University of AmsterdamAmsterdamThe Netherlands
  2. 2.University Children's HospitalMarburgGermany
  3. 3.Laboratory of Pediatrics and NeurologyUniversity Hospital NijmegenThe Netherlands
  4. 4.Department of PediatricsUniversity of LeuvenBelgium
  5. 5.Pediatric ClinicUniversity of CataniaItaly
  6. 6.Children's ClinicSiegenGermany