Leonard, James V.

A Lethal Defect of Mitochondrial and Peroxisomal Fission

Waterham, H. R., Koster, J., van Roermund, C. W. T., Mooyer, P. A. W., Wanders, R. J. A., & Leonard, J. V. (2007) · New England Journal of Medicine

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 749

Recommendations for the management of tyrosinaemia type 1

de Laet, C., Dionisi-Vici, C., Leonard, J. V., McKiernan, P., Mitchell, G., Monti, L., de Baulny, H. O., Pintos-Morell, G., & Spiekerkötter, U. (2013) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 227

Hereditary Tyrosinemia Type I: A New Clinical Classification With Difference in Prognosis on Dietary Treatment

Van Spronsen, F. J., Thomasse, Y., Smit, P. G. A., Leonard, J. V., Clayton, P. T., Fidler, V., Berger, R., & Heymans, H. S. A. (1994) · Hepatology

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 193

HYPERINSULINISM IN ASPHYXIATED AND SMALL-FOR-DATES INFANTS WITH HYPOGLYCAEMIA

Collins, J. E., & Leonard, J. V. (1984) · The Lancet

Pancreatic function and diabetesNeonatal and fetal brain pathology

Cited by 141

Hyperinsulinaemic hypoglycaemia in small for dates babies

Collins, J. E., Leonard, J. V., Teale, D., Marks, V, Williams, D. M., Kennedy, C. R., & Hall, M. A. (1990) · Archives of Disease in Childhood

Pancreatic function and diabetesBirth, Development, and Health

Cited by 110

The Antenatal Diagnosis and Aid to the Management of Hereditary Tyrosinaemia by Use of a Specific and Sensitive GC—MS Assay for Succinylacetone

Pettit, B. R., MacKenzie, F., King, G. S., & Leonard, J. V. (1984) · Organic Acidurias

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 13