spiperone has been researched along with Phenylketonurias in 1 studies
Spiperone: A spiro butyrophenone analog similar to HALOPERIDOL and other related compounds. It has been recommended in the treatment of SCHIZOPHRENIA.
spiperone : An azaspiro compound that is 1,3,8-triazaspiro[4.5]decane which is substituted at positions 1, 4, and 8 by phenyl, oxo, and 4-(p-fluorophenyl)-4-oxobutyl groups, respectively.
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Patients with phenylketonuria (PKU) may suffer from cognitive and neurological deficits which are related to reduced intracerebral concentrations of catecholamines." | 1.29 | Neurotransmitter positron emission tomographic-studies in adults with phenylketonuria, a pilot study. ( Paans, AM; Pruim, J; Smit, GP; Ullrich, K; Visser, G; Willemsen, AT, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Paans, AM | 1 |
| Pruim, J | 1 |
| Smit, GP | 1 |
| Visser, G | 1 |
| Willemsen, AT | 1 |
| Ullrich, K | 1 |
1 other study available for spiperone and Phenylketonurias
| Article | Year |
|---|---|
Neurotransmitter positron emission tomographic-studies in adults with phenylketonuria, a pilot study.
Topics: Adolescent; Adult; Brain; Carbon Radioisotopes; Female; Humans; Male; Phenylalanine; Phenylketonuria | 1996 |