tyrosine has been researched along with Corneal Dystrophies in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Anton-Lamprecht, I; Bohnert, A | 1 |
François, J | 1 |
Gallasch, G; Jaeger, W; Lutz, P; Schmidt, H; Schnyder, UW | 1 |
Garner, A | 2 |
5 other study(ies) available for tyrosine and Corneal Dystrophies
Article | Year |
---|---|
Richner-Hanhart's syndrome: ultrastructural abnormalities of epidermal keratinization indicating a causal relationship to high intracellular tyrosine levels.
Topics: Adult; Child; Corneal Dystrophies, Hereditary; Female; Humans; Intellectual Disability; Keratoderma, Palmoplantar; Male; Middle Aged; Pedigree; Skin; Skin Abnormalities; Syndrome; Tyrosine; Tyrosine Transaminase | 1982 |
Metabolic disorders and corneal changes.
Topics: Amino Acid Metabolism, Inborn Errors; Amyloidosis; Cornea; Corneal Dystrophies, Hereditary; Dysautonomia, Familial; Fabry Disease; Glycogen Storage Disease; Humans; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidoses; Tyrosine | 1981 |
[Herpetiform bilateral epithelial corneal dystrophy caused by Tyrosinemia (Richner-Hanhart-Syndrome) (author's transl)].
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Animals; Corneal Dystrophies, Hereditary; Humans; Infant; Intellectual Disability; Keratoderma, Palmoplantar; Male; Rats; Syndrome; Tyrosine | 1978 |
Hereditary amyloidosis of the cornea.
Topics: Amyloid; Amyloidosis; Arginine; Cornea; Corneal Dystrophies, Hereditary; Humans; Sulfur; Tyrosine | 1970 |
Histochemistry of corneal granular dystrophy.
Topics: Adult; Aged; Amyloid; Arginine; Cornea; Corneal Dystrophies, Hereditary; Epithelium; Eye Proteins; Female; Fibroblasts; Histocytochemistry; Humans; Male; Microscopy, Electron; Middle Aged; Sulfhydryl Compounds; Tryptophan; Tyrosine | 1969 |