Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria

Author:

Fellman Vineta,Rapola Juhani,Pihko Helena,Varilo Teppo,Raivio Kari O

Publisher

Elsevier BV

Subject

General Medicine

Reference23 articles.

1. Pyruvate dehydrogenase E1α deficiency;Brown;J Inherit Metab Dis,1992

2. Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activities;Majander;J Neurol Sci,1995

3. Hepatic morphology and iron quantitation in perinatal hemochromatosis. Comparison with a large perinatal control population, including cases with chronic liver disease;Silver;Am J Pathol,1993

4. Tracing an ancestral mutation: genealogic and haplotype analysis of the infantile onset spinocerebellar ataxia locus;Varilo;Genome Res,1996

5. Lactic acidemia (disorders of pyruvate carboxylase, pyruvate dehydrogenase);Robinson,1995

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