tryptophan has been researched along with Amaurosis in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
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 |
Kawai, K; Seo, A; Sera, H; Tanra, AJ; Yamawaki, S; Yokota, N | 1 |
2 other study(ies) available for tryptophan and Amaurosis
Article | Year |
---|---|
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 |
[Effect of long-term feeding with tryptophan-free diet on the circadian rhythm in rats].
Topics: Animals; Blindness; Brain; Brain Chemistry; Circadian Rhythm; Diet; Hydroxyindoleacetic Acid; Male; Motor Activity; Rats; Rats, Wistar; Receptors, Serotonin; Serotonin; Synaptic Transmission; Tryptophan | 1992 |