arginine has been researched along with Choroid Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kurotaki, J; Miyagawa, Y; Nakazawa, M; Ohguro, H; Sato, M; Yanagihashi, S | 1 |
| Keilhauer, CN; Meigen, T; Weber, BH | 1 |
| Deutman, AF; Heutink, P; Hoyng, CB; Oostra, BA; Pinckers, A; Testers, L | 1 |
| Caruso, RC; Kaiser-Kupfer, MI; Valle, D | 1 |
4 other study(ies) available for arginine and Choroid Diseases
| Article | Year |
|---|---|
Autosomal dominant central areolar choroidal dystrophy and a novel Arg195Leu mutation in the peripherin/RDS gene.
Topics: Aged; Amino Acid Substitution; Arginine; Choroid Diseases; Codon; Electroretinography; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation | 2003 |
Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene.
Topics: Adolescent; Adult; Age of Onset; Arginine; Choroid Diseases; Codon; Disease Progression; DNA Mutational Analysis; Electroretinography; Female; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Visual Acuity | 2006 |
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.
Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Choroid Diseases; Codon; DNA; DNA Mutational Analysis; DNA Primers; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Polymerase Chain Reaction; Retinal Degeneration; Tryptophan | 1996 |
Gyrate atrophy of the choroid and retina: further experience with long-term reduction of ornithine levels in children.
Topics: Adult; Arginine; Choroid Diseases; Diet, Protein-Restricted; Disease Progression; Electroretinography; Female; Fundus Oculi; Gyrate Atrophy; Humans; Male; Nuclear Family; Ornithine; Pedigree; Photography; Retinal Diseases; Visual Acuity; Visual Fields | 2002 |