James V. Leonard

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

Francjan J. van Spronsen, Yolande Thomasse, Peter Smit et al. · Hepatology · 1994 · 194 citations

Medicine, Internal Medicine, Aging +12

A Gene on Chromosome 11q23 Coding for a Putative Glucose- 6-Phosphate Translocase Is Mutated in Glycogen-Storage Disease Types Ib and Ic

Maria Veiga‐da‐Cunha, Isabelle Gerin, Yuan‐Tsong Chen et al. · The American Journal of Human Genetics · 1998 · 123 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Resting energy expenditure in disorders of propionate metabolism

François Feillet, Olaf A. Bodamer, Marjorie Dixon et al. · The Journal of Pediatrics · 2000 · 39 citations

Life Sciences, Biochemistry, Physiology +14

Red blood cell uridine sugar nucleotide levels in patients with classic galactosemia and other metabolic disorders

Gerard T. Berry, Michael J. Palmieri, Simon Heales et al. · Metabolism · 1992 · 32 citations

Life Sciences, Biochemistry, Nutrition +13

Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionate

John H. Walter, Geoffrey N. Thompson, James V. Leonard et al. · Clinica Chimica Acta · 1989 · 24 citations

Life Sciences, Biochemistry, Physiology +2