Screening for Disorders of Tyrosine Metabolism

Author:

Halvorsen S.

Publisher

Springer Berlin Heidelberg

Reference42 articles.

1. Aim J, Larsson A (1979) A follow up of a nationwide neonatal metabolic screening program in Sweden. Pediatr Res 13:79

2. Aronsson S, Engleson G, Jagenburg R, Palmgren B (1968) Long-term dietary treatment of tyrosinosis. J Pediatr 72:620–627

3. Avery ME, Clow CL, Menkes, JH, Ramos A, Scriver CR, Stern L, Wasserman BP (1967) Transient tyrosinemia of the newborn: Dietary and clinical aspects. Pediatrics 39:378–384

4. Bodegaard G, Gentz J, Lindblad B, Lindstedt S, Zetterström R (1969) Hereditary tyrosinemia. III. On the differential diagnosis and the lack of effect of early dietary treatment. Acta Pediatr Scand 58:37–48

5. Bremer HJ, Tosberg P, Hönscher U (1966) Untersuchung über die Tyrosin-Stoffwechselstörung Frühgeborener. I. Veränderungen des Tyrosin-und Phenylalanin-spiegel im Blut Frühgeborener während der ersten Lebenswochen. Ann Paediatr 206:12–27

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1. Disorders of Tyrosine Metabolism;Inborn Metabolic Diseases;2012

2. Inherited Metabolic Rare Disease;Rare Diseases Epidemiology;2010

3. Deficiency of fumarylacetoacetase without hereditary tyrosinemia;Clinical Genetics;2008-04-23

4. Tyrosinemia type I—Diagnostic issues and prenatal diagnosis;The Indian Journal of Pediatrics;2006-02

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