Biochemical monitoring of treatment for galactosaemia: Biological variability in metabolite concentrations

Author:

Hutcheson A. C. J.1,Murdoch-Davis C.2,Green A.1,Preece M. A.1,Allen J.3,Holton J. B.2,Rylance G.1

Affiliation:

1. ; Department of Clinical Chemistry; The Children's Hospital; Birmingham UK

2. ; Department of Biomedical Genetics; FJ Lewis Laboratory, Southmead Hospital; Bristol UK

3. ; Department of Paediatrics; The Children's Hospital; Birmingham UK

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. Ophthalmic findings in classical galactosaemia-prospective study;Beigi;Br J Ophthalmol,1993

2. The effect of dietary fruits and vegetables on urinary galactitol excretion in galactose-1-phosphate uridyltransferase deficiency;Berry;J Inher Metab Dis,1993

3. Endogenous synthesis of galactose in normal men and patients with hereditary galactosaemia;Berry;Lancet,1995

4. Galactonate pathway in normal and GALTde ficient erythrocytes: a new target for aldose reductase inhibitors;Berry;J Inher Metab Dis,1997

5. Measurement error proportional to the mean;Bland;Br Med J,1996

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