galactose has been researched along with Pyruvate Dehydrogenase Complex Deficiency Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Diserens, G; Felser, A; Hertig, D; Kurth, S; Nuoffer, JM; Vermathen, P | 1 |
| Osang, M; Schaub, J | 1 |
| Buncic, JR; Petrova-Benedict, R; Robinson, BH; Wallace, DC | 1 |
3 other study(ies) available for galactose and Pyruvate Dehydrogenase Complex Deficiency Disease
| Article | Year |
|---|---|
Selective galactose culture condition reveals distinct metabolic signatures in pyruvate dehydrogenase and complex I deficient human skin fibroblasts.
Topics: Cell Line; Electron Transport Complex I; Energy Metabolism; Female; Fibroblasts; Galactose; Glucose; Humans; Magnetic Resonance Spectroscopy; Male; Mitochondria; Primary Cell Culture; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Skin | 2019 |
[Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
Topics: Carbohydrate Metabolism, Inborn Errors; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactose; Galactosemias; Glycogen Storage Disease Type I; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type VI; Glycogen Synthase; Humans; Infant; Infant, Newborn; Lactates; Liver; Phosphotransferases; Pyruvate Carboxylase Deficiency Disease; Pyruvate Dehydrogenase Complex Deficiency Disease; Racemases and Epimerases | 1976 |
Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
Topics: Cell Line; Cell Survival; Cells, Cultured; Cytochrome-c Oxidase Deficiency; Fibroblasts; Galactose; Humans; Kearns-Sayre Syndrome; MELAS Syndrome; Mitochondria; Optic Atrophies, Hereditary; Pyruvate Decarboxylase; Pyruvate Dehydrogenase Complex; Pyruvate Dehydrogenase Complex Deficiency Disease; Skin | 1992 |