proline has been researched along with Uveal Diseases in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (100.00) | 18.7374 |
1990's | 0 (0.00) | 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 |
---|---|
Hayasaka, S; Mizuno, K; Omura, K; Saito, T; Tada, K | 1 |
Hayasaka, S; Mizuno, K; Saito, T; Tada, K; Yabata, K | 1 |
Brody, LC; Engelhardt, JF; Kaiser-Kupfer, M; Looney, JE; Mitchell, GA; Obie, C; Patel, AS; Sipila, I; Steel, G; Wong, C | 1 |
3 other study(ies) available for proline and Uveal Diseases
Article | Year |
---|---|
Hyperornithinaemia associated with gyrate atrophy of the choroid and retina: in vivo and in vitro response to vitamin B6.
Topics: Adolescent; Child; Child, Preschool; Choroid; Fibroblasts; Humans; Lymphocytes; Male; Ornithine; Ornithine-Oxo-Acid Transaminase; Proline; Pyridoxine; Retinal Degeneration; Transaminases; Uveal Diseases | 1981 |
Atypical gyrate atrophy of the choroid and retina associated with iminoglycinuria.
Topics: Adult; Atrophy; Choroid; Glycine; Humans; Hydroxyproline; Imino Acids; Macula Lutea; Male; Proline; Retinal Diseases; Uveal Diseases | 1982 |
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
Topics: Alleles; Arginine; Atrophy; Choroid; DNA; Female; Finland; Genes; Humans; Leucine; Male; Mutation; Ornithine-Oxo-Acid Transaminase; Pedigree; Proline; Retina; Retinal Degeneration; Threonine; Transaminases; Uveal Diseases | 1989 |