phenytoin has been researched along with Hypophosphatemia, Familial in 2 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 | 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 |
|---|---|
| Dooling, EC | 1 |
| Stern, L | 1 |
| Verma, IC | 1 |
| Khanna, AR | 1 |
1 review available for phenytoin and Hypophosphatemia, Familial
| Article | Year |
|---|---|
Vitamin D and rickets.
Topics: Acidosis, Renal Tubular; Animals; Bone and Bones; Bone Neoplasms; Calcification, Physiologic; Dihydr | 1973 |
1 other study available for phenytoin and Hypophosphatemia, Familial
| Article | Year |
|---|---|
Hypomagnesemia with convulsions in a newborn infant. Report of a case associated with maternal hypophosphatemia.
Topics: Calcium; Female; Humans; Hypocalcemia; Hypophosphatemia, Familial; Infant, Newborn; Infant, Newborn, | 1967 |