histidine has been researched along with Eye Disorders in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (83.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cunningham, ET; Roe, RH | 1 |
| Couinaud, C | 1 |
| Holmgren, G | 1 |
| Cherikchi, LE | 1 |
| Carson, NA; Martin, VA | 1 |
| Allen, IV; Carson, NA; Chopra, JS; Hurwitz, LJ | 1 |
1 review(s) available for histidine and Eye Disorders
| Article | Year |
|---|---|
[Zinc].
Topics: Acrodermatitis; Animals; Burns; Cicatrix; Congenital Abnormalities; Digestive System Diseases; DNA; Eye Diseases; Genital Diseases, Male; Growth Disorders; Histidine; Humans; Male; Parenteral Nutrition; Proteins; RNA; Zinc | 1984 |
5 other study(ies) available for histidine and Eye Disorders
| Article | Year |
|---|---|
Considering amyloidosis in patients with clinically unresponsive vitreous inflammation (Oculoleptomeningeal amyloidosis in 3 individuals with transthyretin variant Tyr69His. Vol. 44[3]).
Topics: Adrenal Cortex Hormones; Amyloid Neuropathies, Familial; Drug Resistance; Eye Diseases; Genetic Variation; Glycine; Histidine; Humans; Inflammation; Point Mutation; Prealbumin; Tyrosine; Valine; Vitreous Body | 2010 |
Urinary metabolic screening of mentally retarded patients from institutions in the northern part of Sweden.
Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acids; Child; Eye Diseases; Female; Glycine; Glycosaminoglycans; Histidine; Homocystinuria; Humans; Intellectual Disability; Lysine; Male; Mass Screening; Phenylketonurias; Renal Aminoacidurias; Sweden; Syndrome | 1973 |
[Electroelimination in the study of certain characteristics of the pathochemistry and pathogenesis of the inflammatory process in the eye].
Topics: Acute Disease; Chromatography; Chronic Disease; Electric Stimulation Therapy; Exudates and Transudates; Eye Diseases; Histidine; Humans; Inflammation; Uveitis | 1973 |
Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Cataract; Child; Child, Preschool; Cornea; Eye Diseases; Female; Galactosemias; Hepatolenticular Degeneration; Histidine; Homocystinuria; Humans; Infant; Lens, Crystalline; Male; Myopia; Northern Ireland; Pigmentation Disorders; Renal Aminoacidurias | 1967 |
Congenital ophthalmoplegia, floppy baby syndrome, myopathy, and aminoaciduria. Report of a family.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Biopsy; Child; Chromatography, Paper; Chromosomes; Diet Therapy; Electromyography; Eye Diseases; Female; Genes, Recessive; Glycine; Histidine; Humans; Kidney Function Tests; Lysine; Male; Microscopy, Electron; Middle Aged; Muscles; Muscular Diseases; Pedigree; Pelvis | 1969 |