1-anilino-8-naphthalenesulfonate has been researched along with Fuchs' Endothelial Dystrophy in 1 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Fuchs' Endothelial Dystrophy: Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Keratoconus is a condition in which the cornea progressively thins and protrudes in a conical shape, severely affecting refraction and vision." | 1.56 | Association of Genetic Variation With Keratoconus. ( Baird, PN; Burdon, KP; Bykhovskaya, Y; Charlesworth, JC; Craig, JE; Hewitt, AW; Jensen, RA; Li, X; Lucas, SEM; MacGregor, S; Mackey, DA; McComish, BJ; Mills, RA; Mitchell, P; Rabinowitz, YS; Richardson, AJ; Rotter, JI; Sahebjada, S; Taylor, KD; Tenen, A; Wang, JJ; Willoughby, CE, 2020) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 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 | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| McComish, BJ | 1 |
| Sahebjada, S | 1 |
| Bykhovskaya, Y | 1 |
| Willoughby, CE | 1 |
| Richardson, AJ | 1 |
| Tenen, A | 1 |
| Charlesworth, JC | 1 |
| MacGregor, S | 1 |
| Mitchell, P | 1 |
| Lucas, SEM | 1 |
| Mills, RA | 1 |
| Mackey, DA | 1 |
| Li, X | 1 |
| Wang, JJ | 1 |
| Jensen, RA | 1 |
| Rotter, JI | 1 |
| Taylor, KD | 1 |
| Hewitt, AW | 1 |
| Rabinowitz, YS | 1 |
| Baird, PN | 1 |
| Craig, JE | 1 |
| Burdon, KP | 1 |
1 other study available for 1-anilino-8-naphthalenesulfonate and Fuchs' Endothelial Dystrophy
| Article | Year |
|---|---|
Association of Genetic Variation With Keratoconus.
Topics: Adult; Female; Fuchs' Endothelial Dystrophy; Genetic Predisposition to Disease; Genome-Wide Associat | 2020 |