tryptophan has been researched along with Keratoconus in 2 studies
| 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 |
|---|---|
| Franco, W; Lewis, W; Williams, M | 1 |
| Bulman, D; Damji, KF; Gupta, SK; Hussein, N; Jamal, A; Karim, N; Khan, R; Koenekoop, RK; Ladak, SS; Loyer, M; Rahim, M; Sohocki, MM | 1 |
2 other study(ies) available for tryptophan and Keratoconus
| Article | Year |
|---|---|
Loss of Tryptophan Fluorescence Correlates With Mechanical Stiffness Following Photo-Crosslinking Treatment of Rabbit Cornea.
Topics: Animals; Biomechanical Phenomena; Cornea; Cross-Linking Reagents; Disease Models, Animal; Fluorescence; Keratoconus; Male; Photochemotherapy; Photosensitizing Agents; Rabbits; Spectrometry, Fluorescence; Tryptophan | 2017 |
Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p.
Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Aged; Blindness; Carrier Proteins; Child; Child, Preschool; Chromosomes, Human, Pair 17; Codon, Nonsense; Codon, Terminator; Consanguinity; DNA Mutational Analysis; Eye Proteins; Female; Genetic Linkage; Haplotypes; Humans; Keratoconus; Male; Middle Aged; Optic Atrophy, Hereditary, Leber; Pakistan; Pedigree; Polymorphism, Genetic; Retinitis Pigmentosa; Tryptophan | 2001 |