phosphorylethanolamine has been researched along with Hypophosphatemia, Familial 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.
Hypophosphatemia, Familial: An inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME.
| 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 |
|---|---|
| Taillard, F | 1 |
| Desbois, JC | 1 |
| Gueris, J | 1 |
| Delépine, N | 1 |
| Lacour, B | 1 |
| Grétillat, F | 1 |
| Wyart, D | 1 |
1 other study available for phosphorylethanolamine and Hypophosphatemia, Familial
| Article | Year |
|---|---|
[Inorganic pyrophosphates and parathormone in hypophosphatasia. Study of a family].
Topics: Adult; Child, Preschool; Diphosphates; Ethanolamines; Female; Humans; Hypophosphatemia, Familial; In | 1985 |