lactic acid has been researched along with Adult Fanconi Syndrome in 4 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The carnitine concentration was diminished in blood and muscle tissue." | 1.27 | Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity. ( Guggenbichler, JP; Ruitenbeek, W; Sengers, RC; Sperl, W; Stadhouders, AM; Trijbels, JM, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Thirumurugan, A | 1 |
| Thewles, A | 1 |
| Gilbert, RD | 1 |
| Hulton, SA | 1 |
| Milford, DV | 1 |
| Lote, CJ | 1 |
| Taylor, CM | 1 |
| Jonas, AJ | 1 |
| Lin, SN | 1 |
| Conley, SB | 1 |
| Schneider, JA | 1 |
| Williams, JC | 1 |
| Caprioli, RC | 1 |
| Ogier, H | 1 |
| Lombes, A | 1 |
| Scholte, HR | 1 |
| Poll-The, BT | 1 |
| Fardeau, M | 1 |
| Alcardi, J | 1 |
| Vignes, B | 1 |
| Niaudet, P | 1 |
| Saudubray, JM | 1 |
| Sperl, W | 1 |
| Ruitenbeek, W | 1 |
| Trijbels, JM | 1 |
| Sengers, RC | 1 |
| Stadhouders, AM | 1 |
| Guggenbichler, JP | 1 |
4 other studies available for lactic acid and Adult Fanconi Syndrome
| Article | Year |
|---|---|
Urinary L-lactate excretion is increased in renal Fanconi syndrome.
Topics: Adolescent; Child; Child, Preschool; Fanconi Syndrome; Female; Humans; Infant; Lactic Acid; Male | 2004 |
Urine glyceraldehyde excretion is elevated in the renal Fanconi syndrome.
Topics: Child; Cystinosis; Fanconi Syndrome; Gas Chromatography-Mass Spectrometry; Glyceraldehyde; Humans; L | 1989 |
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.
Topics: Brain Diseases, Metabolic; Child, Preschool; Cytochrome-c Oxidase Deficiency; Fanconi Syndrome; Fema | 1988 |
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.
Topics: Acidosis, Lactic; Carnitine; Fanconi Syndrome; Female; Humans; Infant, Newborn; Lactates; Lactic Aci | 1988 |