Hyperphenylalaninaemias-Reference-Cited by-同舟云学术

Hyperphenylalaninaemias

Published:1995 Issue: Volume: Page:147-160
ISSN:
Container-title:Inborn Metabolic Diseases
language:
Short-container-title:

Author:

Smith I.,Brenton D. P.

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/978-3-662-03147-6_12

Reference22 articles.

1. Kaufman S (1987) Tetrahydrobiopterin and hydroxylation systems in health and disease. In: Lovenberg W, Levine RA (eds) Unconjugated pteridines in neurobiology: basic and clinical aspects. Taylor and Francis, London, pp 1–28

2. Smith I (1985) The hyperphenylalaninaemias. In: Lloyd JK, Scriver CR (eds) Genetic and metabolic disease. Butterworth, London, pp 166–210

3. Medical Research Council Working Party on Phenylketonuria (1993) Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Br Med J 306: 115–119

4. Metsuo K, Hommes F (1987) Regional distribution of the phenylalanine sensitive ATP sulphurylase in brain. J Inherited Metab Dis 10: 62–65

5. Bannon MJ, Bunney EB, Roth RH (1981) Mesocortical dopamine neurons: rapid transmitter turnover compared to other brain catecholamine systems. Brain Res 218: 376–382

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