Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines

Multiple Sclerosis

Volumn 4, Issue 1, 1998, Pages 37-38

  Lamers, Karel J B ^a   Wevers, Ron A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Catecholamines; CSF; HVA; L Dopa decarboxylase; Tyrosine hydroxylase

Indexed keywords

AMINO ACID DECARBOXYLASE; BIOGENIC AMINE; CATECHOLAMINE; DOPAMINE BETA MONOOXYGENASE; SEROTONIN; TETRAHYDROBIOPTERIN; TYROSINE 3 MONOOXYGENASE;

ARTICLE; CATECHOLAMINE METABOLISM; CEREBROSPINAL FLUID; INBORN ERROR OF METABOLISM; SEROTONIN METABOLISM;

EID: 0031886637     PISSN: 13524585     EISSN: None     Source Type: Journal    
DOI: 10.1177/135245859800400109     Document Type: Article

References (5)

1. Kaufman S et al. (1975) Phenylketonuria due to deficiency of dihydropteridine reductase. N Engl J Med 293: 785-790.
2. Hyland K. (1993) Abnormalities of biogenic amine metabolism. J Inher Metab Dis 16: 676-690.
3. Hyland K et al. (1992) Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesis. Neurology 42: 1980-1988.
4. Clayton PT et al. (1994) Abstract 32nd Annual Symposium SSIEM, Edinburgh.
5. Lüdecke B, Dworniczak B, Bartholome K. (1995) A point mutation in the hydroxylase gene associated with Segawa syndrome. Hum Genet 95: 123-125.