glycine has been researched along with Familial Hypophosphatemic Rickets in 1 studies
Familial Hypophosphatemic Rickets: A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.
| 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 |
|---|---|
| Shafeghati, Y | 1 |
| Momenin, N | 1 |
| Esfahani, T | 1 |
| Reyniers, E | 1 |
| Wuyts, W | 1 |
1 other study available for glycine and Familial Hypophosphatemic Rickets
| Article | Year |
|---|---|
Vitamin D-dependent rickets type II: report of a novel mutation in the vitamin D receptor gene.
Topics: Alopecia Areata; Child, Preschool; Consanguinity; Exons; Familial Hypophosphatemic Rickets; Female; | 2008 |