ammonium hydroxide has been researched along with Hypophosphatemia, Familial in 2 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
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 | 2 (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 |
|---|---|
| Loiodice, G | 1 |
| Bergamo, F | 1 |
| Bisson, GP | 1 |
| Peretti, L | 1 |
| Reviglio, G | 1 |
| Huguenin, M | 1 |
| Schacht, R | 1 |
| David, R | 1 |
2 other studies available for ammonium hydroxide and Hypophosphatemia, Familial
| Article | Year |
|---|---|
[Case of Lowe's oculo-cerebro-renal syndrome with vitamin D-resistant rickets].
Topics: Ammonia; Child, Preschool; Eye Diseases; Growth Disorders; Humans; Hypophosphatemia, Familial; Intel | 1972 |
Infantile rickets with server proximal renal tubular acidosis, responsive to vitamin D.
Topics: Acidosis, Renal Tubular; Ammonia; Child, Preschool; Dihydrotachysterol; Fanconi Syndrome; Glomerular | 1974 |