malondialdehyde has been researched along with Brain Diseases, Metabolic, Familial in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ellouz, E; Fakhfakh, F; Hadj Salem, I; Jellouli, NK; Kaabachi, N; kamoun, F; Kamoun, Z; tlili, A; Triki, C | 1 |
1 other study(ies) available for malondialdehyde and Brain Diseases, Metabolic, Familial
Article | Year |
---|---|
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Topics: Alcohol Oxidoreductases; Brain Diseases, Metabolic, Inborn; Female; Founder Effect; Glutathione; Humans; Male; Malondialdehyde; Microsatellite Repeats; Mutation; Oxidative Stress; Pedigree; Polymorphism, Single Nucleotide; Tunisia | 2014 |