putrescine has been researched along with Hypophosphatemia, Familial in 1 studies
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 | 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 |
|---|---|
| Lopatin, AN | 1 |
| Shantz, LM | 1 |
| Mackintosh, CA | 1 |
| Nichols, CG | 1 |
| Pegg, AE | 1 |
1 other study available for putrescine and Hypophosphatemia, Familial
| Article | Year |
|---|---|
Modulation of potassium channels in the hearts of transgenic and mutant mice with altered polyamine biosynthesis.
Topics: Animals; Cadaverine; Cells, Cultured; Disease Models, Animal; Hypophosphatemia, Familial; Ion Transp | 2000 |