E A Burgess

Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.

V. G. Oberholzer, B. Levin, E A Burgess et al. · Archives of Disease in Childhood · 1967 · 331 citations · Full text

Metabolic Syndrome, Metabolic Disorder, Methylmalonic Aciduria +9

Hereditary Sucrose Intolerance: Levels of Sucrase Activity in Jejunal Mucosa

E A Burgess, B. Levin, Dilip Mahalanabis et al. · Archives of Disease in Childhood · 1964 · 101 citations · Full text

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

B. Levin, J. M. Abraham, V. G. Oberholzer et al. · Archives of Disease in Childhood · 1969 · 90 citations · Full text

Medicine, Inherited Metabolic Disease, Pathology +1

Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.

B. Levin, R. H. Dobbs, E A Burgess et al. · Archives of Disease in Childhood · 1969 · 64 citations · Full text

Fructosaemia

B. Levin, G. J. A. I. Snodgrass, V. G. Oberholzer et al. · The American Journal of Medicine · 1968 · 63 citations