Compounds > trolamine salicylate
Page last updated: 2024-08-22

trolamine salicylate and Myopia

trolamine salicylate has been researched along with Myopia in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19903 (23.08)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (30.77)24.3611
2020's6 (46.15)2.80

Authors

AuthorsStudies
Choi, SI; Han, J; Jang, JH; Joo, K; Kim, SJ; Lee, BJ; Lim, HT; Oh, BL; Park, JY; So, MK; Woo, SJ1
Alexander, P; Martin, H; Nixon, TRW; Richards, AJ; Snead, MP1
Chen, C; Ding, X; Huang, L; Huang, S; Li, S; Luo, X; Sun, L; Wang, Z1
Jia, X; Li, S; Sun, W; Xiao, X; Zhang, Q1
Chen, C; Ding, X; Huang, L; Li, S; Luo, X; Sun, L; Wang, Z; Zhang, T1
Brejchova, K; Dudakova, L; Liskova, P; Malinka, F; Porter, LF; Skalicka, P1
Laurentino, TS; Marie, SKN; Oba-Shinjo, SM; Soares, RDS1
Claes, C; Collins, F; Flaherty, M; Pinner, J; Schrauwen, I; Sommen, M; Van Camp, G1
Guo, X; Jia, X; Li, J; Li, S; Li, Y; Liang, X; Wang, X; Wei, Y; Xiao, X1
Audran, M; Bouvard, B; Insalaco, P; Legrand, E1
HENKIND, P1
BELAU, PG; FARRELL, FJ; JONES, JD; PUGH, DG; STEINBERG, AG; STICKLER, GB; WARD, LE1
Alvarez de Santos, M; Coronado-Monroy, A; García-Cervantes, ML; González-Quiroga, G; Medinilla-Vázquez, MG; Ramírez-del Río, JL1

Reviews

3 review(s) available for trolamine salicylate and Myopia

ArticleYear
Autosomal Recessive Stickler Syndrome.
    Genes, 2022, 06-24, Volume: 13, Issue:7

    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.
    Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 2020, Volume: 164, Issue:2

    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.
    International journal of molecular sciences, 2019, Jul-23, Volume: 20, Issue:14

    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

Other Studies

10 other study(ies) available for trolamine salicylate and Myopia

ArticleYear
Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1.
    Genes, 2021, 10-05, Volume: 12, Issue:10

    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.
    American journal of ophthalmology, 2020, Volume: 218

    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.
    Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists), 2020, Volume: 40, Issue:3

    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.
    Genes, 2020, 08-03, Volume: 11, Issue:8

    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.
    Clinical genetics, 2014, Volume: 86, Issue:3

    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.
    Molecular vision, 2016, Volume: 22

    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.
    Morphologie : bulletin de l'Association des anatomistes, 2017, Volume: 101, Issue:332

    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.
    Geriatrics, 1965, Volume: 20

    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.
    Mayo Clinic proceedings, 1965, Volume: 40

    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].
    Boletin medico del Hospital Infantil de Mexico, 1986, Volume: 43, Issue:4

    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