trolamine salicylate has been researched along with Myopia in 13 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (23.08) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 4 (30.77) | 24.3611 |
2020's | 6 (46.15) | 2.80 |
Authors | Studies |
---|---|
Choi, SI; Han, J; Jang, JH; Joo, K; Kim, SJ; Lee, BJ; Lim, HT; Oh, BL; Park, JY; So, MK; Woo, SJ | 1 |
Alexander, P; Martin, H; Nixon, TRW; Richards, AJ; Snead, MP | 1 |
Chen, C; Ding, X; Huang, L; Huang, S; Li, S; Luo, X; Sun, L; Wang, Z | 1 |
Jia, X; Li, S; Sun, W; Xiao, X; Zhang, Q | 1 |
Chen, C; Ding, X; Huang, L; Li, S; Luo, X; Sun, L; Wang, Z; Zhang, T | 1 |
Brejchova, K; Dudakova, L; Liskova, P; Malinka, F; Porter, LF; Skalicka, P | 1 |
Laurentino, TS; Marie, SKN; Oba-Shinjo, SM; Soares, RDS | 1 |
Claes, C; Collins, F; Flaherty, M; Pinner, J; Schrauwen, I; Sommen, M; Van Camp, G | 1 |
Guo, X; Jia, X; Li, J; Li, S; Li, Y; Liang, X; Wang, X; Wei, Y; Xiao, X | 1 |
Audran, M; Bouvard, B; Insalaco, P; Legrand, E | 1 |
HENKIND, P | 1 |
BELAU, PG; FARRELL, FJ; JONES, JD; PUGH, DG; STEINBERG, AG; STICKLER, GB; WARD, LE | 1 |
Alvarez de Santos, M; Coronado-Monroy, A; García-Cervantes, ML; González-Quiroga, G; Medinilla-Vázquez, MG; Ramírez-del Río, JL | 1 |
3 review(s) available for trolamine salicylate and Myopia
Article | Year |
---|---|
Autosomal Recessive Stickler Syndrome.
Topics: Arthritis; Child; Connective Tissue Diseases; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; Mutation; Myopia; Osteochondrodysplasias; Pedigree; Retinal Detachment | 2022 |
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 |
LOXL3 Function Beyond Amino Oxidase and Role in Pathologies, Including Cancer.
Topics: Amino Acid Oxidoreductases; Arthritis; Cleft Palate; Collagen; Connective Tissue Diseases; Elastin; Epithelial-Mesenchymal Transition; Extracellular Matrix; Gene Expression Regulation; Hearing Loss, Sensorineural; Humans; Isoenzymes; Myopia; Neoplasms; Organ Specificity; Retinal Detachment; Signal Transduction; Snail Family Transcription Factors; STAT3 Transcription Factor | 2019 |
10 other study(ies) available for trolamine salicylate and Myopia
Article | Year |
---|---|
Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1.
Topics: Adolescent; Adult; Arthritis; Asian People; Child; Child, Preschool; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; Female; Genetic Association Studies; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Infant; Male; Middle Aged; Mutation; Myopia; Pedigree; Phenotype; Republic of Korea; Retinal Detachment; Young Adult | 2021 |
Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing.
Topics: Adolescent; Arthritis; Child; Child, Preschool; Congenital Abnormalities; Connective Tissue Diseases; Cross-Sectional Studies; Developmental Disabilities; Exome Sequencing; Familial Exudative Vitreoretinopathies; Female; Genetic Testing; Hearing Loss, Sensorineural; Humans; Infant; Male; Marfan Syndrome; Myopia; Retinal Detachment; Risk Factors | 2020 |
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndrome.
Topics: Adolescent; Adult; Aged; Arthritis; Child; Collagen Type II; Connective Tissue Diseases; DNA; DNA Mutational Analysis; Female; Hearing Loss, Sensorineural; Humans; Male; Middle Aged; Mutation; Myopia; Pedigree; Retinal Detachment; Time Factors; Young Adult | 2020 |
Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment.
Topics: Adult; Arthritis; Child; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; Female; Hearing Loss, Sensorineural; Humans; Male; Mutation; Myopia; Pedigree; Retinal Detachment | 2020 |
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome.
Topics: Agenesis of Corpus Callosum; Arthritis; Base Sequence; Collagen Diseases; Connective Tissue Diseases; Eye; Hearing Loss, Sensorineural; Hernias, Diaphragmatic, Congenital; Humans; Low Density Lipoprotein Receptor-Related Protein-2; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Myopia; Pedigree; Phenotype; Proteinuria; Renal Tubular Transport, Inborn Errors; Retinal Detachment; Sequence Analysis, DNA | 2014 |
Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome.
Topics: Adolescent; Adult; Arthritis; Asian People; Child; Child, Preschool; China; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; DNA Mutational Analysis; Female; Genetic Association Studies; Hearing Loss, Sensorineural; Humans; Male; Middle Aged; Multiplex Polymerase Chain Reaction; Mutation; Myopia; Pedigree; Retinal Detachment | 2016 |
Osteoporosis in Stickler syndrome. A new family case with bone histology study.
Topics: Adult; Arthritis; Back Pain; Bone and Bones; Child; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; Densitometry; Hearing Loss, Sensorineural; Humans; Male; Mutation; Myopia; Osteoporosis; Phenotype; Radiography; Retinal Detachment | 2017 |
IATROGENIC EYE MANIFESTATIONS IN RHEUMATIC DISEASE.
Topics: Adrenal Cortex Hormones; Arthritis; Arthritis, Rheumatoid; Blindness; Cataract; Conjunctivitis; Diplopia; Drug Therapy; Edema; Eye Diseases; Eye Manifestations; Glaucoma; Gold; Humans; Iatrogenic Disease; Intraocular Pressure; Iridocyclitis; Iritis; Keratitis; Lupus Erythematosus, Systemic; Myopia; Rheumatic Diseases; Salicylates; Spondylitis; Spondylitis, Ankylosing; Toxicology; Uveitis | 1965 |
HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY.
Topics: Arthritis; Biochemical Phenomena; Biochemistry; Blindness; Cataract; Connective Tissue Diseases; Genetics, Medical; Glaucoma; Hearing Loss, Sensorineural; Humans; Joint Diseases; Keratitis; Myopia; Pathology; Radiography; Retinal Detachment; Uveitis | 1965 |
[Stickler syndrome].
Topics: Abnormalities, Multiple; Adult; Arthritis; Bone and Bones; Child; Cleft Palate; Diagnostic Errors; Face; Female; Genes, Dominant; Humans; Male; Middle Aged; Myopia; Pedigree; Pierre Robin Syndrome; Retinal Detachment | 1986 |