Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

1976 • 282 citations

Neurologic Crises in Hereditary Tyrosinemia

1990 • 224 citations

Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean.

1990 • 164 citations

Tyrosinemia

1965 • 130 citations

Inhibition of delta-aminolevulinic acid dehydrase by 4,6-dioxoheptanoic acid.

1981 • 115 citations

Hereditary tyrosinemia type I--an overview.

1986 • 107 citations

Disorders of copper transport

1989 • 96 citations

Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia

1982 • 75 citations

Excretion of δ-aminolevulinic acid in hereditary tyrosinemia

1969 • 68 citations

Four-Hydroxyphenylpyruvic Acid Oxidase Deficiency with Normal Fumarylacetoacetase: a New Variant Form of Hereditary Hypertyrosinemia

1983 • 59 citations

Ionic calcium levels during pregnancy, at delivery and in the first hours of life

1986 • 55 citations

Chronic Tyrosinemia Associated with 4-Hydroxyphenylpyruvate Dioxygenase Deficiency with Acute Intermittent Ataxia and without Visceral and Bone Involvement

1983 • 45 citations

A study of the determination of 5-aminolevulinate hydro-lyase (δ-aminolevulinate dehydratase) activity in hemolysates of human erythrocytes

1971 • 35 citations

Urinary organic acids: isolation and quantification for routine metabolic screening.

1987 • 30 citations

[19] 4-Hydroxyphenylpyruvate dioxygenase from human liver

1987 • 30 citations

Liver cell dysplasia and early liver transplantation in hereditary tyrosinemia.

1990 • 29 citations

Biphasic reduction and concanavalin A binding properties of serum alpha-fetoprotein in preterm and term infants

1991 • 29 citations

Determination of Urinary Succinylacetone by Capillary Gas Chromatography

1984 • 23 citations