arginine has been researched along with Gyrate Atrophy in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (30.77) | 18.2507 |
| 2000's | 4 (30.77) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 3 (23.08) | 2.80 |
| Authors | Studies |
|---|---|
| Bryant, E; Gonik, B; Kanninen, T; Koerner, C | 1 |
| Burr, A; da Palma, MM; Igelman, AD; Koerner, C; Ku, C; Pennesi, ME; Shevchenko Sutherland, L; Valle, D; Yang, P | 1 |
| Bellezza, I; Borri Voltattorni, C; Cellini, B; Desbats, MA; Montioli, R; Salviati, L | 1 |
| Bandello, F; Casalino, G; Manitto, MP; Michaelides, M; Pierro, L | 1 |
| Fiebig, BS; Jägle, H; Renner, AB; Walter, A | 1 |
| Caruso, RC; Kaiser-Kupfer, MI; Reed, GF; Valle, D | 1 |
| Barbier, R; Caron, O; Dollfus, H; Fleury, M; Mohr, M; Tranchant, C; Warter, JM; Ziegler, F | 1 |
| Lawler, AM; Milam, AH; Sipila, I; Steel, G; Valle, D; Wang, T | 1 |
| Brünger, AT; Shah, SA; Shen, BW | 1 |
| Milam, AH; Steel, G; Valle, D; Wang, T | 1 |
| Caruso, RC; Kaiser-Kupfer, MI; Valle, D | 2 |
| Abeling, NG; Bakker, HD; van Gennip, AH; van Schooneveld, MJ; Wanders, RJ | 1 |
1 review(s) available for arginine and Gyrate Atrophy
| Article | Year |
|---|---|
Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects.
Topics: Arginine; Choroid; Chromosomes, Human, Pair 10; Coenzymes; Diet; Gene Expression; Gyrate Atrophy; Humans; Models, Molecular; Mutation; Ornithine; Ornithine-Oxo-Acid Transaminase; Protein Multimerization; Protein Structure, Secondary; Pyridoxal Phosphate; Retina; Vitamin B 6 | 2021 |
12 other study(ies) available for arginine and Gyrate Atrophy
| Article | Year |
|---|---|
First reported case of pregnancy in a patient with ornithine aminotransferase deficiency.
Topics: Amino Acids; Arginine; Atrophy; Female; Gyrate Atrophy; Humans; Ornithine; Ornithine-Oxo-Acid Transaminase; Pregnancy | 2022 |
A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease.
Topics: Arginine; Biomarkers; Diet; Female; Gyrate Atrophy; Humans; Lysine; Middle Aged; Ornithine; Pyridoxine; Tomography, Optical Coherence | 2023 |
Resolution of cystoid macular edema following arginine-restricted diet and vitamin B6 supplementation in a case of gyrate atrophy.
Topics: Arginine; Child; Diet Therapy; Gyrate Atrophy; Humans; Macular Edema; Male; Treatment Outcome; Vitamin B 6 | 2018 |
Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.
Topics: Adult; Arginine; Diet, Protein-Restricted; Electroretinography; Female; Fluorescein Angiography; Follow-Up Studies; Gyrate Atrophy; Humans; Mutation; Ornithine; Ornithine-Oxo-Acid Transaminase; Tomography, Optical Coherence; Visual Acuity; Visual Field Tests; Visual Fields | 2012 |
Use of an arginine-restricted diet to slow progression of visual loss in patients with gyrate atrophy.
Topics: Adolescent; Adult; Aged; Arginine; Child; Diet, Protein-Restricted; Disease Progression; Electroretinography; Female; Follow-Up Studies; Gyrate Atrophy; Humans; Male; Middle Aged; Ornithine; Patient Compliance; Retina; Vision Disorders; Visual Field Tests; Visual Fields | 2004 |
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemia.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Diet, Protein-Restricted; Gyrate Atrophy; Humans; Male; Muscular Diseases; Ornithine; Ornithine-Oxo-Acid Transaminase; Pyridoxine; Vitamin B Complex | 2007 |
Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Arginine; Base Sequence; DNA Primers; Food, Fortified; Genotype; Gyrate Atrophy; Humans; Infant; Lysine; Mammals; Mice; Mice, Mutant Strains; Molecular Sequence Data; Ornithine; Ornithine-Oxo-Acid Transaminase; Phenotype; Polymerase Chain Reaction; Retina; Retinal Degeneration | 1995 |
Human ornithine aminotransferase complexed with L-canaline and gabaculine: structural basis for substrate recognition.
Topics: Aminobutyrates; Arginine; Binding Sites; Crystallography, X-Ray; Cyclohexanecarboxylic Acids; Enzyme Inhibitors; Gyrate Atrophy; Humans; Models, Molecular; Molecular Sequence Data; Ornithine-Oxo-Acid Transaminase; Pyridoxal Phosphate; Transaminases; Tyrosine | 1997 |
Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina.
Topics: Amino Acids; Animals; Arginine; Choroid; Disease Models, Animal; Electroretinography; Gyrate Atrophy; Mice; Mice, Knockout; Ornithine; Ornithine-Oxo-Acid Transaminase; Retina; Retinal Degeneration | 2000 |
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. Long-term reduction of ornithine slows retinal degeneration.
Topics: Adult; Arginine; Child; Child, Preschool; Female; Follow-Up Studies; Fundus Oculi; Genetic Variation; Gyrate Atrophy; Humans; Infant; Longitudinal Studies; Male; Middle Aged; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Degeneration; Treatment Outcome | 1991 |
A far advanced case of gyrate atrophy in a 12-year-old girl.
Topics: Arginine; Child; Diet; Electroencephalography; Electromyography; Female; Gyrate Atrophy; Humans; Myopia; Night Blindness; Ornithine | 1991 |