Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria

Characterization and chromosomal mapping of a genomic clone encoding human alanine:Glyoxylate aminotransferase

P. Edward Purdue, Michael J. Lumb, Margaret Fox et al. · Genomics · 1991 · 136 citations

Life Sciences, Genetics, Molecular Biology +7

Localization of a gene causing cystinuria to chromosome 2p

Elon Pras, Nadir Arber, Ivona Aksentijevich et al. · Nature Genetics · 1994 · 127 citations

Life Sciences, Genetics, Molecular Genetics +9

Urinary oxalate and glycolate excretion and plasma oxalate concentration.

T M Barratt, G. P. Kasidas, IA Murdoch et al. · Archives of Disease in Childhood · 1991 · 88 citations · Full text

Medicine, Nephrology, Obstetrics +9

Urinary oxalate and glycolate excretion in healthy infants and children

Ernst Leumann, Andreas Dietl, A. Matasović · Pediatric Nephrology · 1990 · 64 citations

Medicine, Biochemistry, Pediatrics +10

Hepatic <scp>d</scp>-glycerate dehydrogenase and glyoxylate reductase deficiency in primary hyperoxaluria type 2

J. Mistry, Christopher J. Danpure, R. A. Chalmers · Biochemical Society Transactions · 1988 · 50 citations

Life Sciences, Biochemistry, Pediatrics +12