threonine has been researched along with Retinal Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pelcastre, EL; Villanueva-Mendoza, C; Zenteno, JC | 1 |
| Abe, H; Nakazawa, M; Ohguro, H; Sato, M; Tanimoto, N; Usui, T | 1 |
| Ayala-Ramirez, R; Graue-Wiechers, F; Zenteno, JC | 1 |
| Ichinose, A; Ishikawa, M; Izumi, T; Mori, K; Murata, M; Nakagawa, M; Ooe, A; Takahashi, S | 1 |
4 other study(ies) available for threonine and Retinal Diseases
| Article | Year |
|---|---|
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 |
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 |
Novel CYP4V2 gene mutation in a Mexican patient with Bietti's crystalline corneoretinal dystrophy.
Topics: Aged; Amino Acid Substitution; Corneal Dystrophies, Hereditary; Cytochrome P-450 Enzyme System; Cytochrome P450 Family 4; Cytosine; Diagnostic Techniques, Ophthalmological; Female; Fundus Oculi; Humans; Indians, North American; Isoleucine; Mexico; Mutation; Retinal Diseases; Threonine; Thymine | 2008 |
Ala601-Thr type dysplasminogenaemia genetically diagnosed in patients with retinochoroidal vascular disorders.
Topics: Adult; Aged; Aged, 80 and over; Alanine; Base Sequence; Choroid Diseases; Female; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Peripheral Vascular Diseases; Plasminogen; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Retinal Diseases; Threonine | 1997 |