trolamine salicylate has been researched along with Eye Diseases, Hereditary in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (4.76) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (23.81) | 24.3611 |
| 2020's | 15 (71.43) | 2.80 |
| Authors | Studies |
|---|---|
| Alexander, P; Bale, P; Blackwell, AM; Brown, S; Martin, H; McNinch, AM; Nixon, TRW; Poulson, AV; Richards, AJ; Shenker, N; Snead, MP | 1 |
| Blair, MA; Blair, MP; Khanna, S; Rodriguez, SH; Shapiro, MJ; Wroblewski, K | 1 |
| Belin, PJ; Naravane, AV; Pierce, B; Quiram, PA | 1 |
| Traboulsi, EI | 1 |
| Asano, M; Kimoto, K; Kondo, H; Kubota, T; Matsushita, I; Oku, K; Yokoyama, K | 1 |
| Alexander, P; Martin, H; McNinch, A; Richards, AJ; Snead, MP; Soh, Z | 1 |
| Bhende, M; Bhende, P; Kandale, K; Kandeeban, S; Periyasamy, P; Sarangapani, S; Sinnakaruppan, M | 1 |
| Fang, X; Kong, X; Liu, N; Zhu, C | 1 |
| Alexander, P; Martin, H; Nixon, TRW; Richards, AJ; Snead, MP | 1 |
| Alexander, P; Snead, MP | 1 |
| Kuhn, F; Morris, RE | 1 |
| Acke, FRE; De Leenheer, EMR | 1 |
| Gao, FJ; Hu, FY; Wang, DD; Wu, JH; Xu, P; Zhang, SH | 1 |
| Bath, F; Chinnadurai, S; Roby, BB; Swanson, D; Zavala, H | 1 |
| Baiyasi, A; Barbosa, J; Lin, X; Parendo, A | 1 |
| Besirli, CG; Bohnsack, BL; Branham, KH; Wubben, TJ | 1 |
| Dumitrescu, AV; Zuazo, F | 1 |
| Baron, D; Berrod, JP; Conart, JB | 1 |
| Acland, GM; Aguirre, GD; Goldstein, O; Guyon, R; Johnson, J; Kukekova, A; Kuznetsova, TN; Pearce-Kelling, SE | 1 |
| Chen, TC; Girgis, N | 1 |
| Snead, MP; Yates, JR | 1 |
8 review(s) available for trolamine salicylate and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Dominant Stickler Syndrome.
Topics: Arthritis; Connective Tissue Diseases; Craniofacial Abnormalities; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Osteochondrodysplasias; Pedigree; Retinal Detachment | 2022 |
Autosomal Recessive Stickler Syndrome.
Topics: Arthritis; Child; Connective Tissue Diseases; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Mutation; Myopia; Osteochondrodysplasias; Pedigree; Retinal Detachment | 2022 |
Prevention of Blindness in Stickler Syndrome.
Topics: Arthritis; Blindness; Child; Connective Tissue Diseases; Craniofacial Abnormalities; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Osteochondrodysplasias; Retinal Detachment | 2022 |
Hearing Loss in Stickler Syndrome: An Update.
Topics: Arthritis; Collagen Type IX; Connective Tissue Diseases; Craniofacial Abnormalities; Deafness; Eye Diseases, Hereditary; Hearing Loss; Hearing Loss, Sensorineural; Humans; Mutation; Osteochondrodysplasias; Pedigree; Retinal Detachment | 2022 |
Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review.
Topics: Arthritis; Connective Tissue Diseases; DNA Mutational Analysis; Eye Diseases, Hereditary; Genetic Association Studies; Hearing Loss, Sensorineural; Humans; Mutation; Phenotype; Retinal Detachment | 2020 |
[Degenerative lesions of the peripheral retina].
Topics: Adolescent; Adult; Aged; Arthritis; Collagen Diseases; Connective Tissue Diseases; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Retina; Retinal Degeneration; Retinal Detachment; Retinal Perforations; Retinoschisis | 2014 |
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 |
Clinical and Molecular genetics of Stickler syndrome.
Topics: Abnormalities, Multiple; Arthritis; Child; Child, Preschool; Collagen; Connective Tissue Diseases; Eye Diseases, Hereditary; Face; Humans; Joints; Syndrome | 1999 |
1 trial(s) available for trolamine salicylate and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations.
Topics: Adolescent; Adult; Arthritis; Child; Child, Preschool; Collagen Type II; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Glaucoma; Hearing Loss, Sensorineural; Humans; Infant; Infant, Newborn; Male; Middle Aged; Mutation; Prognosis; Retinal Detachment; Retrospective Studies; Young Adult | 2018 |
12 other study(ies) available for trolamine salicylate and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Stickler syndrome - lessons from a national cohort.
Topics: Adult; Arthritis; Child; Connective Tissue Diseases; Craniofacial Abnormalities; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Mutation; Pedigree; Retinal Detachment | 2022 |
Laser Prophylaxis in Patients with Stickler Syndrome.
Topics: Adolescent; Arthritis; Child; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Hearing Loss, Sensorineural; Humans; Lasers; Retinal Detachment; Retrospective Studies | 2022 |
Risk and Prevention of Retinal Detachments in Patients with Stickler Syndrome.
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Hearing Loss, Sensorineural; Humans; Retinal Detachment; Retinal Perforations; Retrospective Studies | 2022 |
Preventing Retinal Detachment in Patients with Stickler Syndrome: The Effects of Preemptive Laser Photocoagulation.
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Lasers; Light Coagulation; Retinal Detachment | 2022 |
Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in
Topics: Arthritis; Collagen Type II; Connective Tissue Diseases; Eye Diseases, Hereditary; Fluorescein Angiography; Fovea Centralis; Fundus Oculi; Hearing Loss, Sensorineural; Humans; Macular Degeneration; Mutation, Missense; Osteochondrodysplasias; Retinal Detachment; Tomography, Optical Coherence; Vision Disorders | 2022 |
Genetic testing in four Indian families with suspected Stickler syndrome.
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Genetic Testing; Hearing Loss, Sensorineural; Humans; Male; Osteochondrodysplasias; Pedigree; Retinal Degeneration; Retinal Detachment | 2022 |
[Ultrasonographic manifestation and genetic analysis of a fetus with Stickler syndrome].
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Fetus; Hearing Loss, Sensorineural; Humans; Micrognathism; Mutation; Osteochondrodysplasias; Pedigree; Pregnancy; Retinal Detachment; Retrospective Studies | 2022 |
Retinal Detachments in Stickler Syndrome.
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Retinal Detachment | 2022 |
Hearing Outcomes in Stickler Syndrome: Variation Due to
Topics: Arthritis; Child; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; Craniofacial Abnormalities; Eye Diseases, Hereditary; Hearing; Hearing Loss; Hearing Loss, Sensorineural; Humans; Mutation; Osteochondrodysplasias; Retinal Detachment; Retrospective Studies | 2022 |
Pleiotropy of a Stickler syndrome genotype.
Topics: Arthritis; Connective Tissue Diseases; Eye Diseases, Hereditary; Genotype; Hearing Loss, Sensorineural; Humans; Mutation; Pedigree; Phenotype; Retinal Detachment | 2022 |
The uncommon occurrence of two common inherited disorders in a single patient: a mini case series.
Topics: Adolescent; Aged; Arthritis; ATP-Binding Cassette Transporters; Collagen Type XI; Connective Tissue Diseases; Eye Diseases, Hereditary; Female; Hearing Loss, Sensorineural; Humans; Macular Degeneration; Male; Mutation; Prognosis; Retinal Detachment; Stargardt Disease | 2018 |
COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia.
Topics: Animals; Animals, Newborn; Arthritis; Base Sequence; Cataract; Collagen Type IX; Collagen Type XI; Connective Tissue Diseases; Craniofacial Abnormalities; Dog Diseases; Dogs; Dwarfism; Eye Diseases, Hereditary; Female; Genes, Recessive; Genetic Association Studies; Hearing Loss, Sensorineural; Humans; Male; Molecular Sequence Data; Mutation; Osteochondrodysplasias; Pedigree; Retinal Detachment | 2010 |