Vitamin B₁₂ responsive homocystinuria and megaloblastic anemia: Heterogeneity in methylcobalamin deficiency

The Metabolic Basis of Inherited Disease.

1983 • 2,885 citations

Disorders of propionate and methylmalonate metabolism

1982 • 531 citations

Defect in Vitamin B ₁₂ Release from Lysosomes: Newly Described Inborn Error of Vitamin B ₁₂ Metabolism

1985 • 137 citations

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.

1978 • 110 citations

Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.

1984 • 106 citations

Homocystinuria and Megaloblastic Anemia Responsive to Vitamin B₁₂Therapy

1984 • 92 citations

Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells.

1979 • 81 citations

Congenital malabsorption of folate

1970 • 80 citations

Folate Distribution in Cultured Human Cells

1979 • 61 citations

PRENATAL VITAMIN B12 THERAPY OF A FETUS WITH METHYLCOBALAMIN DEFICIENCY (COBALAMIN E DISEASE)

1985 • 60 citations

Genetic patterns of transcobalamin II and the relationships with congenital defects

1983 • 29 citations