trolamine salicylate has been researched along with Intellectual Disability in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (53.33) | 18.7374 |
1990's | 1 (6.67) | 18.2507 |
2000's | 2 (13.33) | 29.6817 |
2010's | 3 (20.00) | 24.3611 |
2020's | 1 (6.67) | 2.80 |
Authors | Studies |
---|---|
Hagen, M; Karempelis, P; Morrell, N; Roby, BB | 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 |
Brogan, P; Compeyrot-Lacassagne, S; Dias, C; Klein, N; Melo Gomes, S; Omoyinmi, E; Sebire, NJ | 1 |
Alessio, M; Anton, J; Boros, C; Brogan, PA; Calvo Penades, I; Cantarini, L; Cattalini, M; Consolini, R; Doglio, M; Frenkel, J; Gattorno, M; Hoppenreijs, E; Insalaco, A; Jeyaratnam, J; Lachmann, HJ; Lane, T; Lepore, L; Martini, A; Martino, S; Modesto, C; Pachlopnik Schmid, J; Quartier, P; Rigante, D; Ruperto, N; Russo, R; Simon, A; Ter Haar, NM | 1 |
Offit, PA | 1 |
RAUNIO, P; VAHVANEN, V | 1 |
HUEBNER, R; ROMANIUK, PA | 1 |
Magaña, S; Smith, MJ | 1 |
Griscelli, C; Prieur, AM | 1 |
Hansen, US; Herlin, T | 1 |
Lampert, F | 1 |
Gussen, R | 1 |
Dociu, I; Galaction-Nitelea, O; Murgu, V; Sirjita, N | 1 |
Holmes, LB; Rosenblatt, D | 1 |
Ballivet, J; Binnert, D; Loche, D | 1 |
15 other study(ies) available for trolamine salicylate and Intellectual Disability
Article | Year |
---|---|
Associated syndromes in patients with Pierre Robin Sequence.
Topics: 22q11 Deletion Syndrome; Adolescent; Arthritis; Arthrogryposis; Child; Child, Preschool; Chromosome Disorders; Cleft Palate; Clubfoot; Connective Tissue Diseases; De Lange Syndrome; Duane Retraction Syndrome; Female; Hand Deformities, Congenital; Hearing Loss, Sensorineural; Heart Defects, Congenital; Humans; Hypoventilation; Infant; Infant, Newborn; Intellectual Disability; Male; Mandibulofacial Dysostosis; Mobius Syndrome; Muscle Hypotonia; Pierre Robin Syndrome; Retinal Detachment; Retrospective Studies; Sleep Apnea, Central | 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 |
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry.
Topics: Abdominal Pain; Adolescent; Age of Onset; Amyloidosis; Arthralgia; Arthritis; Cerebellar Diseases; Child; Child, Preschool; Conjunctivitis; Diarrhea; Female; Genotype; Headache; Humans; Infant; Infant, Newborn; Intellectual Disability; Lymphadenopathy; Male; Mevalonate Kinase Deficiency; Myalgia; Pharyngitis; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Registries; Retrospective Studies; Skin Diseases; Stomatitis, Aphthous; Uveitis; Vomiting | 2016 |
The power of 'box a'.
Topics: Adult; Arthritis; Autistic Disorder; Causality; Child, Preschool; Cohort Studies; Decision Making; Denmark; Humans; Infant; Intellectual Disability; Lyme Disease Vaccines; Measles-Mumps-Rubella Vaccine; Parents; Pertussis Vaccine; Public Opinion; Retrospective Studies; Risk; Vaccination | 2003 |
[WEBER-CHRISTIAN SYNDROME].
Topics: Abducens Nerve Diseases; Arthritis; Genetic Diseases, X-Linked; Humans; Intellectual Disability; Osteochondrodysplasias; Panniculitis; Panniculitis, Nodular Nonsuppurative | 1964 |
[PANNICULITIS NODOSA (PFEIFER-WEBER-CHRISTIAN SYNDROME) A RARE PECULIAR INFLAMMATION OF THE ADIPOSE TISSUE. CONTRIBUTION TO THE DIFFERENTIAL DIAGNOSIS OF LIPOID CALCINOGRANULOMATOSIS].
Topics: Abducens Nerve Diseases; Adipose Tissue; Arthritis; Arthritis, Rheumatoid; Diagnosis, Differential; Genetic Diseases, X-Linked; Geriatrics; Hip Joint; Humans; Inflammation; Intellectual Disability; Osteochondrodysplasias; Panniculitis; Panniculitis, Nodular Nonsuppurative; Radiography | 1964 |
Health outcomes of midlife and older Latina and black American mothers of children with developmental disabilities.
Topics: Adolescent; Adult; Aged; Arthritis; Black People; Caregivers; Child; Cross-Sectional Studies; Depression; Developmental Disabilities; Disability Evaluation; Female; Health Surveys; Hispanic or Latino; Humans; Intellectual Disability; Middle Aged; Morbidity; Mothers; Reference Values; United States; White People | 2006 |
Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation.
Topics: Adolescent; Arthritis; Cephalometry; Child, Preschool; Eye Diseases; Female; Humans; Intellectual Disability; Knee Joint; Male; Meningitis; Neutrophils; Parapsoriasis; Radiography | 1981 |
Chronic arthritis in a boy with 18q- syndrome.
Topics: Abnormalities, Multiple; Adolescent; Arthritis; Chromosome Deletion; Chromosomes, Human, Pair 18; Chronic Disease; Humans; Intellectual Disability; Male | 1994 |
Infantile multisystem inflammatory disease: another case of a new syndrome.
Topics: Arthritis; Child, Preschool; Chronic Disease; Female; Humans; Inflammation; Intellectual Disability; Syndrome; Urticaria | 1986 |
Unusual lesion of incudomalleal joint.
Topics: Adult; Arthritis; Autopsy; Bronchopneumonia; Ear Ossicles; Epilepsy, Tonic-Clonic; Female; Humans; Intellectual Disability; Middle Aged; Otitis Media; Sclerosis; Staining and Labeling; Synovial Membrane | 1971 |
[Centrofacial lentiginosis. Observations on 9 patients].
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.
Topics: Abnormalities, Multiple; Adult; Arthritis; Eye Diseases; Humans; Intellectual Disability; Renal Aminoacidurias; Syndrome | 1974 |
[Familial disease with ulcero-mutilans acropathia, pyramidal syndrome and debility].
Topics: Adolescent; Adult; Arthritis; Bone Diseases; Female; Finger Joint; Foot Dermatoses; Humans; Intellectual Disability; Leg Ulcer; Pedigree; Pyramidal Tracts | 1970 |