arginine has been researched along with Retinal Diseases in 20 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (20.00) | 18.7374 |
| 1990's | 2 (10.00) | 18.2507 |
| 2000's | 10 (50.00) | 29.6817 |
| 2010's | 3 (15.00) | 24.3611 |
| 2020's | 1 (5.00) | 2.80 |
| Authors | Studies |
|---|---|
| El-Bradey, MH; Elhawary, EE; Elshanshory, MR; Khedr, SF; Nagy, HM | 1 |
| Mohan, R; Wizeman, JW | 1 |
| Bhattacharya, SK | 1 |
| Biemond, BJ; Brandjes, DP; Duits, AJ; Landburg, PP; Muskiet, FA; Schnog, JB; Teerlink, T | 1 |
| Pelcastre, EL; Villanueva-Mendoza, C; Zenteno, JC | 1 |
| Honda, Y; Katsuta, H; Kiryu, J; Miyahara, S; Miyamoto, K; Nishijima, K; Nonaka, A; Tsujikawa, A; Yamashiro, K | 1 |
| Abe, H; Nakazawa, M; Ohguro, H; Sato, M; Tanimoto, N; Usui, T | 1 |
| Liu, C; Varnum, MD | 1 |
| Berjukow, S; Beyl, S; Hering, S; Hohaus, A; Kudrnac, M; Marksteiner, R; Maw, MA; Timin, EN | 1 |
| Edwards, AO; Zhuk, SA | 1 |
| Muthulakshmi, R; Nallathambi, J; Namperumalsamy, P; Rajendran, A; Shukla, D; Sundaresan, P | 1 |
| Boman, H; Bredrup, C; Knappskog, PM; Rødahl, E | 1 |
| Visek, WJ | 1 |
| Berson, EL; Hanson, AH; Rosner, B; Shih, VE | 1 |
| Arjomaa, P; Simell, O; Sipilä, I | 1 |
| Almog, J; Geyer, O; Lazar, M; Lupu-Meiri, M; Oron, Y | 1 |
| Fuchs, S; Gal, A; Kellner, U; Wedemann, H | 1 |
| Birch, DG; Bowne, SJ; Daiger, SP; Heckenlively, JR; Lewis, RA; Mintz-Hittner, H; Northrup, H; Rodriquez, JA; Ruiz, RS; Saperstein, DA; Sohocki, MM; Sullivan, LS | 1 |
| Caruso, RC; Kaiser-Kupfer, MI; Valle, D | 1 |
| Marliss, EB; McCulloch, C | 1 |
2 review(s) available for arginine and Retinal Diseases
| Article | Year |
|---|---|
Retinal deimination in aging and disease.
Topics: Aging; Arginine; Humans; Hydrolases; Neurodegenerative Diseases; Protein Processing, Post-Translational; Protein-Arginine Deiminase Type 2; Protein-Arginine Deiminases; Retinal Diseases | 2009 |
An update of concepts of essential amino acids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Ammonia; Animals; Arginine; Atrophy; Child; Choroid; Dietary Proteins; Female; Glucose Tolerance Test; Growth; Histidine; Humans; Insulin; Kidney Failure, Chronic; Male; Middle Aged; Nitrogen; Nutritional Requirements; Orotic Acid; Pregnancy; Retinal Diseases; Reye Syndrome; Urea; Uveal Diseases; Wounds and Injuries | 1984 |
1 trial(s) available for arginine and Retinal Diseases
| Article | Year |
|---|---|
A two year trial of low protein, low arginine diets or vitamin B6 for patients with gyrate atrophy.
Topics: Adolescent; Adult; Arginine; Atrophy; Child; Choroid; Clinical Trials as Topic; Dietary Proteins; Female; Genes, Recessive; Humans; Ornithine; Pyridoxine; Retinal Diseases; Uveal Diseases | 1982 |
17 other study(ies) available for arginine and Retinal Diseases
| Article | Year |
|---|---|
Correlation of Asymmetric Dimethyl Arginine Level to Sickle Retinopathy in Children With Sickle Cell Disease.
Topics: Anemia, Sickle Cell; Arginine; Child; Cross-Sectional Studies; Humans; Retinal Diseases | 2023 |
Expression of peptidylarginine deiminase 4 in an alkali injury model of retinal gliosis.
Topics: Animals; Arginine; Burns, Chemical; Citrulline; Eye Burns; Female; Gliosis; Hydrolases; Male; Mice; Protein-Arginine Deiminase Type 4; Retina; Retinal Diseases; Sodium Hydroxide | 2017 |
Plasma asymmetric dimethylarginine concentrations in sickle cell disease are related to the hemolytic phenotype.
Topics: Adult; Albuminuria; Anemia, Sickle Cell; Arginine; beta-Thalassemia; Cholelithiasis; Female; Hemolysis; Humans; Hypertension, Pulmonary; Leg Ulcer; Male; Middle Aged; Nitric Oxide; Osteonecrosis; Phenotype; Priapism; Retinal Diseases; Sickle Cell Trait; Young Adult | 2010 |
Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.
Topics: Adult; Arginine; Base Sequence; Child, Preschool; Exudates and Transudates; Eye Diseases; Eye Proteins; Genes, X-Linked; Haplotypes; Humans; Infant, Newborn; Male; Mutation, Missense; Nerve Tissue Proteins; Pedigree; Rare Diseases; Recurrence; Retinal Diseases; Threonine; Ultrasonography; Vitreous Body; Young Adult | 2010 |
Argatroban attenuates leukocyte- and platelet-endothelial cell interactions after transient retinal ischemia.
Topics: Animals; Arginine; Blood Platelets; Cell Adhesion; Disease Models, Animal; Endothelium, Vascular; Gene Expression; Intercellular Adhesion Molecule-1; Ischemia; Leukocytes; Male; P-Selectin; Partial Thromboplastin Time; Pipecolic Acids; Platelet Aggregation Inhibitors; Prothrombin Time; Rats; Rats, Long-Evans; Reperfusion; Retina; Retinal Diseases; Retinal Vessels; RNA, Messenger; Sulfonamides; Thrombin; Treatment Outcome; Vascular Patency | 2003 |
Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies.
Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Calcium-Binding Proteins; Electroretinography; Female; Fundus Oculi; Genes, Dominant; Genetic Testing; Glycine; Guanylate Cyclase-Activating Proteins; Humans; Isoleucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Retinal Diseases; Threonine; Visual Fields | 2005 |
Functional consequences of progressive cone dystrophy-associated mutations in the human cone photoreceptor cyclic nucleotide-gated channel CNGA3 subunit.
Topics: Animals; Arginine; Cyclic Nucleotide-Gated Cation Channels; Cysteine; Disease Progression; Electrophysiology; Female; Histidine; Humans; Ion Channel Gating; Ion Channels; Mutation; Oocytes; Patch-Clamp Techniques; Protein Isoforms; Retinal Cone Photoreceptor Cells; Retinal Diseases; Xenopus laevis | 2005 |
Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Amino Acid Sequence; Arginine; Barium; Calcium; Calcium Channels, L-Type; Cell Line; Green Fluorescent Proteins; Humans; Ions; Isoleucine; Kinetics; Membrane Potentials; Microscopy, Confocal; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Phenotype; Protein Conformation; Protein Structure, Tertiary; Retinal Diseases; Time Factors; Transfection | 2005 |
Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion.
Topics: Age of Onset; Aged; Aged, 80 and over; Arginine; Atrophy; Bestrophins; Chloride Channels; Eye Proteins; Female; Fundus Oculi; Humans; Intermediate Filament Proteins; Macula Lutea; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Peripherins; Proline; Prospective Studies; Retinal Diseases; Visual Acuity | 2006 |
Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.
Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Asian People; Cysteine; Exons; Exudates and Transudates; Eye Diseases; Fluorescein Angiography; Frizzled Receptors; Fundus Oculi; Humans; India; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Proline; Receptors, G-Protein-Coupled; Retinal Diseases; Serine; Vitreous Body | 2006 |
Clinical manifestation of a novel PAX6 mutation Arg128Pro.
Topics: Adult; Aged; Arginine; Cataract; Corneal Opacity; Eye Diseases, Hereditary; Eye Proteins; Female; Fovea Centralis; Homeodomain Proteins; Humans; Iris; Male; Middle Aged; Mutation, Missense; Nystagmus, Pathologic; Paired Box Transcription Factors; PAX6 Transcription Factor; Pedigree; Proline; Repressor Proteins; Retinal Diseases; Tomography, Optical Coherence | 2008 |
Gyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginine.
Topics: Adolescent; Adult; Amidinotransferases; Arginine; Atrophy; Child; Choroid; Creatine; Female; Glycine; Guanidines; Humans; Male; Ornithine; Retina; Retinal Diseases; Uveal Diseases | 1980 |
Nitric oxide synthase inhibitors protect rat retina against ischemic injury.
Topics: Animals; Arginine; Cell Count; Enzyme Inhibitors; Guanidines; Intraocular Pressure; Ischemia; Male; Nitric Oxide; Nitric Oxide Synthase; Nitroarginine; Rats; Rats, Sprague-Dawley; Retinal Diseases; Retinal Ganglion Cells; Retinal Vessels | 1995 |
Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy.
Topics: Adult; Arginine; Blindness; Genetic Linkage; Humans; Male; Mutation; Retinal Diseases; Vitreoretinopathy, Proliferative; X Chromosome | 1995 |
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.
Topics: Amino Acid Substitution; Animals; Arginine; Cysteine; Genetic Variation; Glutamine; Homeodomain Proteins; Humans; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Mutation; Nerve Tissue Proteins; Optic Atrophies, Hereditary; Peripherins; Prevalence; Proline; Retinal Degeneration; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Trans-Activators; Tyrosine | 2001 |
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 |
Gyrate atrophy of the choroid and retina: clinical, ophthalmologic, and biochemical considerations.
Topics: Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Atrophy; Cataract; Choroid; Histidine; Humans; Male; Muscles; Muscular Atrophy; Ornithine; Retinal Diseases; Retinal Vessels; Uveal Diseases; Visual Fields | 1975 |