proline has been researched along with Eye Disorders in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chang, MH; Demirci, FY; Gorin, MB; Mah, TS; Romero, MF | 1 |
| Muthulakshmi, R; Nallathambi, J; Namperumalsamy, P; Rajendran, A; Shukla, D; Sundaresan, P | 1 |
| Ferlini, A; Forabosco, A; Gobbi, P; Mencucci, R; Michelucci, R; Plasmati, R; Salvi, F; Salvi, G; Santangelo, M; Volpe, R | 1 |
| Greco, GM; Magli, A | 1 |
| Naess, O; Nicolaissen, B; Ringvold, A | 1 |
| Duvall, J; Goldberg, MF; Puck, A; Sugar, J; Tso, MO; Yue, BY | 1 |
1 review(s) available for proline and Eye Disorders
| Article | Year |
|---|---|
[Eye manifestations of amino acid disorders].
Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates | 1978 |
5 other study(ies) available for proline and Eye Disorders
| Article | Year |
|---|---|
Proximal renal tubular acidosis and ocular pathology: a novel missense mutation in the gene (SLC4A4) for sodium bicarbonate cotransporter protein (NBCe1).
Topics: Acidosis, Renal Tubular; Adult; Amino Acid Sequence; Animals; Base Sequence; Biological Transport; Cell Membrane; Eye Diseases; Homozygote; Humans; Leucine; Male; Molecular Sequence Data; Mutation, Missense; Oocytes; Proline; Sodium-Bicarbonate Symporters; Xenopus | 2006 |
Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.
Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Asian People; Cysteine; Exons; Exudates and Transudates; Eye Diseases; Fluorescein Angiography; Frizzled Receptors; Fundus Oculi; Humans; India; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Proline; Receptors, G-Protein-Coupled; Retinal Diseases; Serine; Vitreous Body | 2006 |
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families.
Topics: Adult; Aged; Alanine; Amyloidosis; Eye Diseases; Female; Humans; Lens Diseases; Male; Middle Aged; Mutation; Pedigree; Prealbumin; Proline; Ultrasonography; Vitreous Body | 1993 |
Amino acid incorporation in cell cultures from eyes with pseudo-exfoliation material.
Topics: Anterior Eye Segment; Cells, Cultured; Conjunctival Diseases; Extracellular Matrix; Eye Diseases; Humans; Leucine; Proline | 1992 |
Nanophthalmic sclera. Morphologic and tissue culture studies.
Topics: Adult; Cells, Cultured; Eye Diseases; Eye Proteins; Fundus Oculi; Glycosaminoglycans; Humans; Hyaluronic Acid; Male; Microscopy, Electron; Proline; Sclera | 1986 |