phenylacetic acid has been researched along with Thalassemia in 1 studies
phenylacetic acid : A monocarboxylic acid that is toluene in which one of the hydrogens of the methyl group has been replaced by a carboxy group.
Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
| Excerpt | Relevance | Reference |
|---|---|---|
| "(c) Hereditary spherocytosis was singly differentiated by an elevated acetylcholinesterase activity with acetylthiocholine and by a vastly diminished sensitivity to stearic acid, while activity with phenylacetate was equal to control." | 1.27 | Unique profile for erythrocyte membrane acetylcholinesterase in hereditary spherocytosis. ( Klin, A; Livne, A; Streichman, S; Tatarsky, I, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Streichman, S | 1 |
| Klin, A | 1 |
| Tatarsky, I | 1 |
| Livne, A | 1 |
1 other study available for phenylacetic acid and Thalassemia
| Article | Year |
|---|---|
Unique profile for erythrocyte membrane acetylcholinesterase in hereditary spherocytosis.
Topics: Acetylcholinesterase; Acetylthiocholine; Anemia, Dyserythropoietic, Congenital; Anemia, Hemolytic, A | 1983 |