trolamine salicylate has been researched along with Eye Abnormalities in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Brejchova, K; Dudakova, L; Liskova, P; Malinka, F; Porter, LF; Skalicka, P | 1 |
Hayashi, T; Kimoto, K; Kondo, H; Kubota, T; Kusaka, S; Matsushita, I; Nagata, T; Ohji, M | 1 |
Chen, TC; Girgis, N | 1 |
DeCunto, C; Denda, L; Dollfus, H; Dufier, JL; Gonzales, LD; Häfner, R; Hofmann, HM; Jorge, JP; Melo-Gomez, J; Premoli, J; Prieur, AM; Russo, RA; Stubna, M; Vesely, R | 1 |
Katsicas, MM; Russo, RA | 1 |
Velzeboer, CM | 1 |
2 review(s) available for trolamine salicylate and Eye Abnormalities
Article | Year |
---|---|
Brittle cornea syndrome: Disease-causing mutations in ZNF469 and two novel variants identified in a patient followed for 26 years.
Topics: Adult; Arthritis; Connective Tissue Diseases; Corneal Edema; Corneal Perforation; Diagnostic Errors; Eye Abnormalities; Glaucoma; Hearing Loss, Sensorineural; Heterozygote; Humans; Joint Instability; Keratoplasty, Penetrating; Male; Myopia; Reoperation; Retinal Detachment; Skin Abnormalities; Trabeculectomy; Transcription Factors; Vitrectomy | 2020 |
Genetics of the pediatric glaucomas.
Topics: Aniridia; Anterior Eye Segment; Arthritis; Child; Collagen Type XI; Connective Tissue Diseases; Corneal Opacity; Eye Abnormalities; Eye Diseases, Hereditary; Glaucoma; Glaucoma, Open-Angle; Hearing Loss, Sensorineural; Humans; Nail-Patella Syndrome; Neurofibromatosis 1; Oculocerebrorenal Syndrome; Retinal Detachment; Sturge-Weber Syndrome; Turner Syndrome; Vitreous Detachment | 2011 |
4 other study(ies) available for trolamine salicylate and Eye Abnormalities
Article | Year |
---|---|
Foveal Hypoplasia in Patients with Stickler Syndrome.
Topics: Adolescent; Adult; Arthritis; Child; Child, Preschool; Collagen Type II; Connective Tissue Diseases; Cross-Sectional Studies; Eye Abnormalities; Female; Fluorescein Angiography; Fovea Centralis; Hearing Loss, Sensorineural; Humans; Male; Middle Aged; Mutation; Retinal Detachment; Retrospective Studies; Tomography, Optical Coherence; Visual Acuity; Young Adult | 2017 |
Chronic infantile neurological cutaneous and articular/neonatal onset multisystem inflammatory disease syndrome: ocular manifestations in a recently recognized chronic inflammatory disease of childhood.
Topics: Abnormalities, Multiple; Adolescent; Adult; Anterior Eye Segment; Arthritis; Child; Child, Preschool; Chronic Disease; Eye Abnormalities; Eye Diseases; Female; Fluorescein Angiography; Humans; Male; Meningitis; Optic Atrophy; Optic Disk; Papilledema; Skin Diseases; Syndrome; Uveitis, Anterior; Visual Acuity | 2000 |
Chronic infantile neurological cutaneous and articular syndrome: two new cases with rare manifestations.
Topics: Abnormalities, Multiple; Antirheumatic Agents; Arthritis; Azathioprine; Child, Preschool; Chronic Disease; Developmental Disabilities; Diagnosis, Differential; Exanthema; Eye Abnormalities; Female; Humans; Immunosuppressive Agents; Infant; Male; Syndrome | 2001 |
Clinical demonstrations.
Topics: Adolescent; Adult; Angiokeratoma; Arthritis; Child; Conjunctivitis; Cornea; Eye Abnormalities; Eye Diseases; Facial Neoplasms; Female; Glaucoma; Humans; Joint Dislocations; Lens, Crystalline; Male; Neurilemmoma; Postoperative Complications; Retinal Degeneration; Retinitis Pigmentosa; Vaccinia | 1970 |