glycine has been researched along with Eye Diseases, Hereditary in 2 studies
Eye Diseases, Hereditary: Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bekheirnia, MR | 1 |
| Reed, B | 1 |
| Gregory, MC | 1 |
| McFann, K | 1 |
| Shamshirsaz, AA | 1 |
| Masoumi, A | 1 |
| Schrier, RW | 1 |
| O'Hearn, TM | 1 |
| Fawzi, A | 1 |
| He, S | 1 |
| Rao, NA | 1 |
| Lim, JI | 1 |
2 other studies available for glycine and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Genotype-phenotype correlation in X-linked Alport syndrome.
Topics: Adult; Age of Onset; Collagen Type IV; Eye Diseases, Hereditary; Genotype; Glycine; Hearing Loss; Hu | 2010 |
Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.
Topics: Adult; Age of Onset; Amyloid Neuropathies, Familial; Asian People; Eye Diseases, Hereditary; Fluores | 2007 |