glycine has been researched along with Hypophosphatemia, Familial in 3 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 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Holmgren, G | 1 |
| Lindqvist, B | 1 |
| Lundberg, E | 1 |
| Econs, MJ | 1 |
| Pericak-Vance, MA | 1 |
| Betz, H | 1 |
| Bartlett, RJ | 1 |
| Speer, MC | 1 |
| Drezner, MK | 1 |
| Perkoff, GT | 1 |
1 review available for glycine and Hypophosphatemia, Familial
| Article | Year |
|---|---|
The hereditary renal diseases.
Topics: Acidosis, Renal Tubular; Bone Diseases; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria | 1967 |
2 other studies available for glycine and Hypophosphatemia, Familial
| Article | Year |
|---|---|
Hyperaminoaciduria in mild phosphate diabetes in adults.
Topics: Adult; Cystine; Cystinuria; Female; Glutamine; Glycine; Humans; Hypophosphatemia, Familial; Male; Mi | 1980 |
The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene.
Topics: Female; Genes; Genetic Linkage; Genetic Markers; Glycine; Humans; Hypophosphatemia, Familial; Lod Sc | 1990 |