Page last updated: 2024-08-22

trolamine salicylate and Abnormalities, Multiple

trolamine salicylate has been researched along with Abnormalities, Multiple in 19 studies

Research

Studies (19)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (21.05)	18.7374
1990's	2 (10.53)	18.2507
2000's	9 (47.37)	29.6817
2010's	4 (21.05)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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
Brogan, P; Compeyrot-Lacassagne, S; Dias, C; Klein, N; Melo Gomes, S; Omoyinmi, E; Sebire, NJ	1
Egbert, M; Gonzalez, M; Guerrero, CA; Van Sickels, JE	1
Altun, G; Glucksman, MJ; Martignetti, JA; Mosig, R; Sancak, S; Tuysuz, B	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
Camacho, C; Evans, BR; Glucksman, MJ; Grum-Tokars, V; Lobl, M; Martignetti, CR; Martignetti, JA; Mosig, RA	1
Emami Nia, A; Emaminia, A; Kashef, S; Mousavi Nasab, M; Nabavi, M	1
Hansen, US; Herlin, T	1
Snead, MP; Yates, JR	1
Al Aqeel, A; Al Sewairi, W; Desnick, RJ; Edress, B; Gorlin, RJ; Martignetti, JA	1
DeCunto, C; Denda, L; Dollfus, H; Dufier, JL; Gonzales, LD; Häfner, R; Hofmann, HM; Jorge, JP; Melo-Gomez, J; Premoli, J; Prieur, AM; Russo, RA; Stubna, M; Vesely, R	1
Vu, TH	1
Katsicas, MM; Russo, RA	1
Helin, P; Jacobsen, GK; Matthiesen, G; Nielsen, NS; Pedersen, VF	1
Chouery, E; Delague, V; Medlej-Hashim, M; Mégarbané, A; Sanders, A; Torbey, PH	1
Alvarez de Santos, M; Coronado-Monroy, A; García-Cervantes, ML; González-Quiroga, G; Medinilla-Vázquez, MG; Ramírez-del Río, JL	1
Preblud, SR	1
Dociu, I; Galaction-Nitelea, O; Murgu, V; Sirjita, N	1
Holmes, LB; Rosenblatt, D	1

Reviews

1 review(s) available for trolamine salicylate and Abnormalities, Multiple

Article	Year
Clinical and Molecular genetics of Stickler syndrome. Journal of medical genetics, 1999, Volume: 36, Issue:5 Topics: Abnormalities, Multiple; Arthritis; Child; Child, Preschool; Collagen; Connective Tissue Diseases; Eye Diseases, Hereditary; Face; Humans; Joints; Syndrome	1999

Other Studies

18 other study(ies) available for trolamine salicylate and Abnormalities, Multiple

Article	Year
STAT3 gain of function: a new aetiology of severe rheumatic disease. Rheumatology (Oxford, England), 2019, 02-01, Volume: 58, Issue:2 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. Pediatrics, 2019, Volume: 144, Issue:1 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
Vertical and horizontal mandibular lengthening of the ramus and body. Atlas of the oral and maxillofacial surgery clinics of North America, 2008, Volume: 16, Issue:2 Topics: Abnormalities, Multiple; Adolescent; Adult; Airway Obstruction; Ankylosis; Arthritis; Arthroplasty; Child; Dentition, Mixed; Facial Asymmetry; Female; Humans; Infant; Male; Mandible; Osteogenesis, Distraction; Osteotomy; Syndrome; Temporomandibular Joint Disorders; Vertical Dimension	2008
A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects. European journal of human genetics : EJHG, 2009, Volume: 17, Issue:5 Topics: Abnormalities, Multiple; Arthritis; Base Sequence; Binding Sites; Child; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Hajdu-Cheney Syndrome; Heart Defects, Congenital; Hemopexin; Humans; Male; Matrix Metalloproteinase 2; Models, Molecular; Mutation; Pedigree; Protein Structure, Tertiary; Syndrome; Turkey	2009
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients. European journal of human genetics : EJHG, 2010, Volume: 18, Issue:8 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
Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome. American journal of human genetics, 2012, Sep-07, Volume: 91, Issue:3 Topics: Abnormalities, Multiple; Amino Acid Sequence; Arthritis; Contracture; Corneal Opacity; Female; Growth Disorders; Hajdu-Cheney Syndrome; Humans; Matrix Metalloproteinase 14; Models, Molecular; Mutation; Osteolysis; Osteoporosis; Radiography	2012
Central nervous system involvement in Blau syndrome: a new feature of the syndrome? The Journal of rheumatology, 2007, Volume: 34, Issue:12 Topics: Abnormalities, Multiple; Adult; Arthritis; Central Nervous System Diseases; Child; Eye Diseases; Female; Humans; Male; Skin Diseases; Syndrome	2007
Chronic arthritis in a boy with 18q- syndrome. The Journal of rheumatology, 1994, Volume: 21, Issue:10 Topics: Abnormalities, Multiple; Adolescent; Arthritis; Chromosome Deletion; Chromosomes, Human, Pair 18; Chronic Disease; Humans; Intellectual Disability; Male	1994
Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family. American journal of medical genetics, 2000, Jul-03, Volume: 93, Issue:1 Topics: Abnormalities, Multiple; Adult; Arthritis; Consanguinity; Female; Humans; Male; Osteolysis, Essential; Pedigree; Radiography; Saudi Arabia; Syndrome	2000
Chronic infantile neurological cutaneous and articular/neonatal onset multisystem inflammatory disease syndrome: ocular manifestations in a recently recognized chronic inflammatory disease of childhood. Archives of ophthalmology (Chicago, Ill. : 1960), 2000, Volume: 118, Issue:10 Topics: Abnormalities, Multiple; Adolescent; Adult; Anterior Eye Segment; Arthritis; Child; Child, Preschool; Chronic Disease; Eye Abnormalities; Eye Diseases; Female; Fluorescein Angiography; Humans; Male; Meningitis; Optic Atrophy; Optic Disk; Papilledema; Skin Diseases; Syndrome; Uveitis, Anterior; Visual Acuity	2000
Don't mess with the matrix. Nature genetics, 2001, Volume: 28, Issue:3 Topics: Abnormalities, Multiple; Arthritis; Extracellular Matrix; Humans; Matrix Metalloproteinase 2; Osteolysis; Syndrome; Transforming Growth Factor beta	2001
Chronic infantile neurological cutaneous and articular syndrome: two new cases with rare manifestations. Acta paediatrica (Oslo, Norway : 1992), 2001, Volume: 90, Issue:9 Topics: Abnormalities, Multiple; Antirheumatic Agents; Arthritis; Azathioprine; Child, Preschool; Chronic Disease; Developmental Disabilities; Diagnosis, Differential; Exanthema; Eye Abnormalities; Female; Humans; Immunosuppressive Agents; Infant; Male; Syndrome	2001
Winchester syndrome. International orthopaedics, 2001, Volume: 25, Issue:5 Topics: Abnormalities, Multiple; Arthritis; Child; Contracture; Corneal Diseases; Follow-Up Studies; Growth Disorders; Hand Deformities, Acquired; Humans; Infant; Male; Methotrexate; Orthopedic Procedures; Osteolysis, Essential; Radiography; Severity of Illness Index; Syndrome; Treatment Outcome	2001
An unknown autoinflammatory syndrome associated with short stature and dysmorphic features in a young boy. The Journal of rheumatology, 2002, Volume: 29, Issue:5 Topics: Abnormalities, Multiple; Arthritis; Body Height; Child; Developmental Disabilities; Edema; Fever of Unknown Origin; Fingers; Humans; Male; Orbit; Pain; Subcutaneous Tissue	2002
[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
Some current issues relating to rubella vaccine. JAMA, 1985, Jul-12, Volume: 254, Issue:2 Topics: Abnormalities, Multiple; Adult; Antibodies, Viral; Arthritis; Child; Female; Humans; Infant, Newborn; Joint Diseases; Male; Pain; Pregnancy; Risk; Rubella; Rubella Vaccine; Rubella virus; Syndrome; Time Factors	1985
[Centrofacial lentiginosis. Observations on 9 patients]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1972, Volume: 23, Issue:9 Topics: Abnormalities, Multiple; Adolescent; Adult; Arthritis; Bone and Bones; Child; Cryptorchidism; Humans; Hypothalamic Diseases; Infant; Intellectual Disability; Lentigo; Male; Microcephaly; Middle Aged; Skull; Spinal Diseases; Spine	1972
Letter: Development of arthritis in Lowe's syndrome. The Journal of pediatrics, 1974, Volume: 84, Issue:6 Topics: Abnormalities, Multiple; Adult; Arthritis; Eye Diseases; Humans; Intellectual Disability; Renal Aminoacidurias; Syndrome	1974