Journal of Inherited Metabolic Disease

, Volume 23, Issue 4, pp 313–316 | Cite as

Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment

  • A. B. Burlina
  • L. Bonafé
  • V. Ferrari
  • A. Suppiej
  • F. Zacchello
  • A. P. Burlina
Article

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REFERENCES

  1. Braütigam C, Wevers RA, Jansen RJT, et al (1998) Biochemical hallmarks of tyrosine hydroxylase deficiency. Clin Chem 44: 1897–1904.Google Scholar
  2. Burgard P, Bremer HJ, Bührdel P, et al (1999) Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997. Eur J Pediatr 158: 46–54.Google Scholar
  3. Burlina AP, Ferrari V, Divry P, et al (1999) N-Acetylaspartylglutamate in Canavan disease: an adverse effector?Eur J Pediatr 158: 406–409.Google Scholar
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  7. Scriver CR, Kaufmann S, Eisensmith RC, Woo SLC (1995) The hyperphenylalaninemias. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1015–1075.Google Scholar

Copyright information

© Kluwer Academic Publishers 2000

Authors and Affiliations

  • A. B. Burlina
    • 1
  • L. Bonafé
    • 2
  • V. Ferrari
    • 3
  • A. Suppiej
    • 1
  • F. Zacchello
    • 1
  • A. P. Burlina
    • 4
  1. 1.Department of PaediatricsUniversity of PadovaPadovaItaly
  2. 2.Division of Clinical Chemistry and BiochemistryUniversity Children's HospitalZürichSwitzerland
  3. 3.Department of Veterinary MedicineUniversity of PadovaPadovaItaly
  4. 4.Department of Neurological and Psychiatric SciencesUniversity of PadovaPadovaItaly

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