trolamine salicylate has been researched along with Facies in 6 studies
| 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 | 5 (83.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bochet, P; Marotte, H; Ramond, F; Thomas, T; Touraine, R | 1 |
| Antunes, O; Baque-Juston, M; Fabre, A; Forbes, LR; Giovannini-Chami, L; Hiéronimus, S; Leroy, S; Roux, C; Tieulié, N; Trojani, MC; Vincent-Mefitiot, N; Vogel, TP | 1 |
| Anand, D; Buckley, M; Colley, A; Cowley, MJ; Dinger, M; Ewans, LJ; Forneris, F; Gaston-Massuet, C; Giunta, C; Gualtieri, A; Kirk, EP; Lachke, SA; McCabe, MJ; Miller, D; Roscioli, T; Scietti, L; Sillence, D; Walsh, C; Ying, K; Zhu, Y | 1 |
| Brogan, P; Compeyrot-Lacassagne, S; Dias, C; Klein, N; Melo Gomes, S; Omoyinmi, E; Sebire, NJ | 1 |
| Athanasakis, E; Biskup, S; Bruno, I; D'Adamo, AP; Esposito, L; Faletra, F; Gasparini, P | 1 |
| Acke, FR; De Leenheer, EM; De Pauw, GA; Dhooge, IJ; Malfait, F | 1 |
1 review(s) available for trolamine salicylate and Facies
| Article | Year |
|---|---|
Pathogenic variants in
Topics: Adolescent; Adult; Animals; Arthritis; Comparative Genomic Hybridization; Connective Tissue Diseases; Disease Models, Animal; Exome Sequencing; Facies; Female; Gene Expression; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Hearing Loss, Sensorineural; Humans; Immunohistochemistry; Male; Mice; Models, Molecular; Mutation; Pedigree; Phenotype; Phylogeny; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Protein Conformation; Retinal Detachment; Structure-Activity Relationship; Vascular Diseases; Young Adult | 2019 |
5 other study(ies) available for trolamine salicylate and Facies
| Article | Year |
|---|---|
Arthritis associated to cardio-facio-cutaneous syndrome related to a MAP2K1 mutation.
Topics: Arthritis; Ectodermal Dysplasia; Facies; Failure to Thrive; Heart Defects, Congenital; Humans; MAP Kinase Kinase 1; Mutation | 2020 |
STAT3 gain of function: a new aetiology of severe rheumatic disease.
Topics: Abnormalities, Multiple; Arthritis; Autoimmune Diseases; Contracture; Facies; Female; Gain of Function Mutation; Growth Disorders; Humans; Intellectual Disability; Intestinal Diseases; Lung Diseases, Interstitial; Microcephaly; Rheumatic Diseases; STAT3 Transcription Factor; Young Adult | 2019 |
Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome.
Topics: Abnormalities, Multiple; Anti-Inflammatory Agents, Non-Steroidal; Arthritis; Child; Codon, Nonsense; Diagnosis, Differential; DNA-Binding Proteins; Etanercept; Face; Facies; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Hypotrichosis; Intellectual Disability; Male; Methotrexate; Micrognathism; Neck; Transcription Factors | 2019 |
Autosomal recessive Stickler syndrome due to a loss of function mutation in the COL9A3 gene.
Topics: Adolescent; Arthritis; Bone and Bones; Child; Child, Preschool; Collagen Diseases; Collagen Type IX; Connective Tissue Diseases; DNA Mutational Analysis; Facies; Female; Genes, Recessive; Hearing Loss; Hearing Loss, Sensorineural; Homozygote; Humans; Male; Mutation; Pedigree; Radiography; Retinal Detachment | 2014 |
Cephalometrics in Stickler syndrome: Objectification of the typical facial appearance.
Topics: Adolescent; Adult; Arthritis; Cephalometry; Child; Cleft Palate; Collagen Type XI; Connective Tissue Diseases; Facies; Female; Hearing Loss, Sensorineural; Humans; Male; Mandible; Middle Aged; Mutation; Retinal Detachment; Vitreous Detachment; Young Adult | 2016 |