phenylacetic acid has been researched along with Hemoglobinuria, Paroxysmal 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phenylacetic acid : A monocarboxylic acid that is toluene in which one of the hydrogens of the methyl group has been replaced by a carboxy group.
Hemoglobinuria, Paroxysmal: A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins.
| 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 Hemoglobinuria, Paroxysmal
| Article | Year |
|---|---|
Unique profile for erythrocyte membrane acetylcholinesterase in hereditary spherocytosis.
Topics: Acetylcholinesterase; Acetylthiocholine; Anemia, Dyserythropoietic, Congenital; Anemia, Hemolytic, A | 1983 |