Urine glyceraldehyde excretion is elevated in the renal Fanconi syndrome
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Kidney International
- Vol. 35 (1) , 99-104
- https://doi.org/10.1038/ki.1989.14
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome.Journal of Clinical Investigation, 1985
- Defective Galactose Oxidation in a Patient with Glycogen Storage Disease and Fanconi SyndromePediatric Research, 1983
- The Fanconi syndrome and mechanisms of tubular transport dysfunctionKidney International, 1981
- Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome‐c‐oxidase deficiencyNeurology, 1980
- The fanconi syndrome associated with hepatic glycogenosis and abnormal metabolism of galactoseThe Journal of Pediatrics, 1974
- Fructosaemia: Observations on seven casesThe American Journal of Medicine, 1968
- Tyrosinemia: An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debré-Fanconi syndrome)The Journal of Pediatrics, 1965
- The Amino-aciduria in GalactosaemiaArchives of Disease in Childhood, 1955
- Cystine Storage Disease with Aminoaciduria and Dwarfism (LIGNAC—FANCONI DISEASE): INTRODUCTIONActa Paediatrica, 1952
- Der nephrotisch-glykosurische Zwergwuchs mit hypophosphatämischer Rachitis1Deutsche Medizinische Wochenschrift (1946), 1936