Compounds > proline

proline and Uveal Diseases

proline has been researched along with Uveal Diseases in 3 studies

Research

Studies (3)

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

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

Other Studies

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. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2 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. Archives of ophthalmology (Chicago, Ill. : 1960), 1982, Volume: 100, Issue:3 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. Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:1 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