Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment-Reference-Cited by-同舟云学术

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

Published:2000-06 Issue:4 Volume:23 Page:313-316
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Burlina A. B.¹,Bonafé L.²,Ferrari V.³,Suppiej A.¹,Zacchello F.¹,Burlina A. P.⁴

Affiliation:

1. ; Department of Paediatrics; University of Padova; Padova Italy

2. ; Division of Clinical Chemistry and Biochemistry; University Children's Hospital; Zürich Switzerland

3. ; Department of Veterinary Medicine; University of Padova; Padova Italy

4. ; Department of Neurological and Psychiatric Sciences; University of Padova; Padova Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005694122277/fullpdf

Reference7 articles.

1. Biochemical hallmarks of tyrosine hydroxylase deficiency;Braütigam;Clin Chem,1998

2. Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997;Burgard;Eur J Pediatr,1999

3. N-Acetylaspartylglutamate in Canavan disease: an adverse effector ?;Burlina;Eur J Pediatr,1999

4. Recommendations on the dietary management of phenylketonuria;Medical Research Council Working Party on Phenylketonuria.;Arch Dis Child,1993

5. Neurological outcome in adult patients with early-treated phenylketonuria;Pietz;Eur J Pediatr,1998

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