Results of Long-Term Treatment with Orthophosphate and Pyridoxine in Patients with Primary Hyperoxaluria
Open Access
- 8 December 1994
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 331 (23), 1553-1558
- https://doi.org/10.1056/nejm199412083312304
Abstract
The prognosis for patients with primary hyperoxaluria has been ominous, with the expectation of renal failure, poor results with transplantation, and early death.This publication has 34 references indexed in Scilit:
- Primary hyperoxaluria type IEuropean Journal of Pediatrics, 1990
- Reversal by Liver Transplantation of the Complications of Primary Hyperoxaluria as Well as the Metabolic DefectNew England Journal of Medicine, 1989
- Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1Journal of Inherited Metabolic Disease, 1989
- An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.The Journal of cell biology, 1989
- Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.Journal of Histochemistry & Cytochemistry, 1988
- SUCCESSFUL TREATMENT OF PRIMARY HYPEROXALURIA TYPE I BY COMBINED HEPATIC AND RENAL TRANSPLANTATIONThe Lancet, 1987
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986
- A simple estimate of glomerular filtration rate in adolescent boysThe Journal of Pediatrics, 1985
- Primary Hyperoxaluria (Glycolic Acid Variant)Upsala Journal of Medical Sciences, 1978
- PRIMARY HYPEROXALURIAMedicine, 1964