phosphorylethanolamine has been researched along with Infant, Premature, Diseases in 1 studies
phosphorylethanolamine: RN given refers to parent cpd; structure
O-phosphoethanolamine : The ethanolamine mono-ester of phosphoric acid, and a metabolite of phospholipid metabolism. This phosphomonoester shows strong structural similarity to the inhibitory neurotransmitter GABA, and is decreased in post-mortem Alzheimer's disease brain.
Infant, Premature, Diseases: Diseases that occur in PREMATURE INFANTS.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hypophosphatasia is a rare genetic disease characterized by deficiency of tissue-nonspecific alkaline phosphatase (TNSALP) activity, excessive urinary excretion of phosphoethanolamine, poor bone mineralization and skeletal anomalies." | 1.33 | Neonatal hypophosphatasia and seizures. A case report. ( Meli, C; Palazzo, P; Romeo, DM; Smilari, P; Sorge, G, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Smilari, P | 1 |
| Romeo, DM | 1 |
| Palazzo, P | 1 |
| Meli, C | 1 |
| Sorge, G | 1 |
1 other study available for phosphorylethanolamine and Infant, Premature, Diseases
| Article | Year |
|---|---|
Neonatal hypophosphatasia and seizures. A case report.
Topics: Chromatography, Ion Exchange; Ethanolamines; Humans; Hypophosphatasia; Infant; Infant, Newborn; Infa | 2005 |