trolamine salicylate has been researched along with Craniofacial Abnormalities in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (16.67) | 29.6817 |
| 2010's | 4 (33.33) | 24.3611 |
| 2020's | 6 (50.00) | 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 |
| Alexander, P; Martin, H; McNinch, A; Richards, AJ; Snead, MP; Soh, Z | 1 |
| Alexander, P; Snead, MP | 1 |
| Acke, FRE; De Leenheer, EMR | 1 |
| Janssen, EJM; Stegmann, APA; Stumpel, CTRM | 1 |
| Bath, F; Chinnadurai, S; Roby, BB; Swanson, D; Zavala, H | 1 |
| Hasegawa, K; Higuchi, Y; Tanaka, H; Tsukahara, H; Yamashita, M | 1 |
| Fujii, M; Kinouchi, K; Nishio, J; Tachibana, K; Takeuchi, M | 1 |
| Beemer, FA; Bendix, L; Björck, E; Bonduelle, M; Boute, O; Cormier-Daire, V; Coucke, PJ; De Buyzere, M; De Die-Smulders, C; De Paepe, A; Dewinter, C; Dieux-Coeslier, A; Dollfus, H; Elting, M; Green, A; Guerci, VI; Hennekam, RC; Hilhorts-Hofstee, Y; Holder, M; Hoornaert, KP; Hoyng, C; Jones, KJ; Josifova, D; Kaitila, I; Kjaergaard, S; Kroes, YH; Lagerstedt, K; Lees, M; Lemerrer, M; Leroy, BP; Leroy, JG; Magnani, C; Marcelis, C; Martorell, L; Mathieu, M; McEntagart, M; Mendicino, A; Mortier, GR; Morton, J; Orazio, G; Paquis, V; Reish, O; Rosenberg, T; Simola, KO; Smithson, SF; Temple, KI; Van Aken, E; Van Bever, Y; van den Ende, J; Van Hagen, JM; Vereecke, I; Zelante, L; Zordania, R | 1 |
| Acland, GM; Aguirre, GD; Goldstein, O; Guyon, R; Johnson, J; Kukekova, A; Kuznetsova, TN; Pearce-Kelling, SE | 1 |
| Chen, Y; Colarossi, C; Dabovic, B; Obata, H; Rifkin, DB; Zambuto, L | 1 |
| Abe, E; Apte, SS; Aqeel, AA; Bianco, P; DiFeo, A; Diouri, J; Doty, SB; Dowling, O; Madri, J; Majeska, RJ; Martignetti, JA; Mosig, RA; Oblander, SA; Parker, IC; Ramirez, MC; Schaffler, MB; Wylie, JD; Zaidi, M | 1 |
4 review(s) available for trolamine salicylate and Craniofacial Abnormalities
| Article | Year |
|---|---|
Dominant Stickler Syndrome.
Topics: Arthritis; Connective Tissue Diseases; Craniofacial Abnormalities; Eye Diseases, Hereditary; Hearing Loss, Sensorineural; Humans; 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 |
A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature.
Topics: Arthritis; Cataract; Child; Child, Preschool; Cleft Palate; Collagen Type II; Collagen Type XI; Connective Tissue Diseases; Craniofacial Abnormalities; Diagnosis, Differential; Growth Disorders; Hearing Loss, Sensorineural; Humans; Male; Micrognathism; Mutation; Osteochondrodysplasias; Palate, Soft; Phenotype; Retinal Detachment | 2017 |
8 other study(ies) available for trolamine salicylate and Craniofacial Abnormalities
| 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 |
Distinguishing Marshall from Stickler syndrome: a clinical and genetic challenge.
Topics: Alleles; Arthritis; Cataract; Collagen Type XI; Connective Tissue Diseases; Craniofacial Abnormalities; Diagnosis, Differential; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Genotype; Hearing Loss, Sensorineural; Humans; Infant; Male; Osteochondrodysplasias; Phenotype; Retinal Detachment | 2021 |
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 |
Perioperative management of 19 infants undergoing glossopexy (tongue-lip adhesion) procedure: a retrospective study.
Topics: Airway Management; Arthritis; Connective Tissue Diseases; Craniofacial Abnormalities; Female; Fiber Optic Technology; Hearing Loss, Sensorineural; Humans; Infant; Infant, Newborn; Intubation, Intratracheal; Lip; Male; Mandibulofacial Dysostosis; Perioperative Care; Pierre Robin Syndrome; Retinal Detachment; Retrospective Studies; Tongue; Tracheostomy | 2015 |
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.
Topics: Abnormalities, Multiple; Arthritis; Cleft Palate; Collagen Type II; Connective Tissue Diseases; Craniofacial Abnormalities; DNA Mutational Analysis; Genetic Association Studies; Hearing Loss, Sensorineural; Humans; Retinal Detachment; Sequence Analysis, DNA; Sequence Analysis, RNA | 2010 |
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 |
Bone defects in latent TGF-beta binding protein (Ltbp)-3 null mice; a role for Ltbp in TGF-beta presentation.
Topics: Adaptor Proteins, Signal Transducing; Animals; Arthritis; Biomarkers; Blotting, Northern; Bone and Bones; Carrier Proteins; Cartilage, Articular; Craniofacial Abnormalities; Gene Targeting; Hedgehog Proteins; Immunohistochemistry; In Situ Hybridization; Latent TGF-beta Binding Proteins; Mice; Mice, Knockout; Parathyroid Hormone-Related Protein; Peptide Hormones; Trans-Activators | 2002 |
Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth.
Topics: Animals; Arthritis; Bone and Bones; Bone Remodeling; Calcification, Physiologic; Cell Proliferation; Cells, Cultured; Craniofacial Abnormalities; Gene Deletion; Humans; Immunohistochemistry; Joints; Matrix Metalloproteinase 2; Mice; Mice, Knockout; Osteoblasts; Osteoclasts; Reverse Transcriptase Polymerase Chain Reaction; RNA, Small Interfering; Time Factors; Tomography, X-Ray Computed | 2007 |