V. G. Oberholzer

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

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

BIOCHEMICAL INVESTIGATIONS OF HYPERAMMONÆMIA

B. Levin, V. G. Oberholzer, Lynn Sinclair · The Lancet · 1969 · 73 citations

Hyperthermia, Biochemistry, Biochemical Taxonomy +7

Fructosaemia

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

Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.

B. E. Kendall, D. P. E. Kingsley, James V. Leonard et al. · Journal of Neurology Neurosurgery & Psychiatry · 1983 · 62 citations · Full text

Neuropsychology, Corticobasal Degeneration, Neurological Disorder +18