arginine has been researched along with Night Blindness in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dryja, TP; Fishman, GA; Hajali, M; Lindeman, M; Sweeney, MO | 1 |
Fishman, GA; Grover, S; Stone, EM | 1 |
Abeling, NG; Bakker, HD; van Gennip, AH; van Schooneveld, MJ; Wanders, RJ | 1 |
3 other study(ies) available for arginine and Night Blindness
Article | Year |
---|---|
Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.
Topics: Alcohol Oxidoreductases; Arginine; Child; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Glutamine; Glycine; Humans; Hypopigmentation; Mutation, Missense; Night Blindness; Photic Stimulation; Retina; Retinal Cone Photoreceptor Cells; Retinal Pigments; Retinal Rod Photoreceptor Cells; Sensory Thresholds; Tryptophan; Vision, Ocular; Visual Fields | 2009 |
A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Child; Child, Preschool; Electroretinography; Female; Genes, Dominant; Humans; IMP Dehydrogenase; Male; Night Blindness; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Proline; Retinitis Pigmentosa; Visual Acuity; Visual Fields | 2004 |
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 |