malondialdehyde has been researched along with Anemia, Hemolytic, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Condara, H; Dolan, J; Fortier, NL; Jacobs, J; Sauberman, N; Snyder, LM; Szymanski, I | 1 |
| Alvarez, R; Beutler, E; Callis, M; Corrons, JL; Gelbart, T; Lasheras, G; Oliva, E; Pujades, A; Ribes, A; Zarza, R | 1 |
| Fairbanks, G; Fortier, NL; Harm, W; Lutz, HU; Snyder, LM | 1 |
1 review(s) available for malondialdehyde and Anemia, Hemolytic, Hereditary
| Article | Year |
|---|---|
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies.
Topics: Adult; Anemia, Hemolytic, Congenital; Erythrocytes; Female; Glutathione Synthase; Humans; Infant; Male; Malondialdehyde; Middle Aged; Point Mutation; Polymorphism, Single-Stranded Conformational; Pyrrolidonecarboxylic Acid; Reverse Transcriptase Polymerase Chain Reaction; Spain | 2001 |
2 other study(ies) available for malondialdehyde and Anemia, Hemolytic, Hereditary
| Article | Year |
|---|---|
Red cell membrane response to hydrogen peroxide-sensitivity in hereditary xerocytosis and in other abnormal red cells.
Topics: Anemia, Hemolytic, Congenital; Anemia, Sickle Cell; Desiccation; Electrophoresis, Polyacrylamide Gel; Erythrocyte Membrane; Erythrocytes; Erythrocytes, Abnormal; Humans; Hydrogen Peroxide; Malondialdehyde; Methemoglobin; Osmotic Fragility; Potassium; Thalassemia | 1981 |
Increased erythrocyte lipid peroxidation in hereditary xerocytosis.
Topics: Anemia, Hemolytic, Congenital; Cell Membrane Permeability; Cholesterol; Erythrocytes; Fatty Acids; Humans; Lipid Peroxides; Malondialdehyde; Phospholipids | 1979 |