trolamine salicylate has been researched along with Chronic Infantile Neurologic, Cutaneous, and Articular Syndrome in 13 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 | 10 (76.92) | 24.3611 |
| 2020's | 3 (23.08) | 2.80 |
| Authors | Studies |
|---|---|
| Carapito, R; DeCauwer, A; Georgel, P; Lévy, D; Macquin, C; Mariotte, A; Maurier, F; Meyer, A; Molitor, A; Pichot, A | 1 |
| Abu-Shukair, M; Abushhaiwia, A; Al-Mayouf, SM; Albrawi, S; AlEnazi, A; AlMosawi, Z; Almuatiri, M; Almuatiri, N; Almutairi, A; Alsonbul, A; Alwahadneh, A; Alzyoud, R; Fathalla, BM; Khawaja, E; Khawaja, K; Madan, W; Zlenti, M | 1 |
| Bonnekoh, H; Butze, M; Kallinich, T; Kambe, N; Kokolakis, G; Krause, K | 1 |
| Brizi, MG; Cantarini, L; Caso, F; Galeazzi, M; Guerrini, S; Lucherini, OM; Magnotti, F; Muscari, I; Patti, M; Punzi, L; Rigante, D; Vitale, A | 1 |
| Al-Mayouf, SM; Bader-Meunier, B; Cantarini, L; Frenkel, J; Gattorno, M; Gérard, L; Hofer, M; Insalaco, A; Koné-Paut, I; Kuemmerle-Deschner, J; Lachmann, HJ; Levy, R; Martini, A; Martino, S; Meini, A; Modesto, C; Naselli, A; Neven, B; Nikishina, I; Ozen, S; Quartier, P; Ruperto, N; Schwarz, T; Woo, P | 1 |
| Bacherini, D; Bascherini, V; Cantarini, L; Emmi, G; Franceschini, R; Frediani, B; Granato, C; Iannone, F; Lopalco, G; Messina, M; Molinaro, F; Rigante, D; Salerni, A; Selmi, C; Vannozzi, L | 1 |
| Alix, L; Bedane, C; Berthelot, JM; Bonnet, C; Cathebras, P; Cuisset, L; Devauchelle-Pensec, V; Duffau, P; Duquesne, A; Fischbach, M; Frances, C; Gaillard, D; Garcier, F; Grall-Lerosey, M; Grateau, G; Guennoc, X; Hachulla, E; Hamidou, M; Houx, L; Jurquet, AL; Kone-Paut, I; Le Blay, P; Le Jeunne, C; Lemelle, I; Lequerré, T; Morell-Dubois, S; Neven, B; Pagnier, A; Pillet, P; Quartier, P; Richez, C; Smail, A; Stirnemann, J; Touitou, I; Touraine, R; Tran, TA | 1 |
| Angermair, E; Deuter, C; Doycheva, D; Kuemmerle-Deschner, J; Sobolewska, B; Zierhut, M | 1 |
| Shen, M; Wu, D | 1 |
| Afraei, S; Azizi, G; Ghiasy, S; Khadem Azarian, S; Khan Nazer, NH; Mirshafiey, A; Mohebi, A; Mosayebian, A; Nazeri, S; Sadri, G | 1 |
| Cassel, SL; Wilson, SP | 1 |
| Beck, PL; Mason, DR; Muruve, DA | 1 |
| Ibrahim, S; Pei, TS; Ping, TS; Sridharan, R; Zaki, FM | 1 |
7 review(s) available for trolamine salicylate and Chronic Infantile Neurologic, Cutaneous, and Articular Syndrome
| Article | Year |
|---|---|
Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms.
Topics: Arthritis; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Immunologic Deficiency Syndromes; Interferons; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Interleukin-18; Phospholipase C gamma; Sarcoidosis; Skin Diseases, Genetic; Synovitis; Uveitis | 2020 |
Biological treatments: new weapons in the management of monogenic autoinflammatory disorders.
Topics: Acne Vulgaris; Anemia, Dyserythropoietic, Congenital; Arthritis; Arthritis, Infectious; Biological Products; Cranial Nerve Diseases; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Immunologic Deficiency Syndromes; Inflammation; Intracellular Signaling Peptides and Proteins; Mevalonate Kinase Deficiency; Mutation; Osteomyelitis; Pyoderma Gangrenosum; Receptors, Interleukin-1; Sarcoidosis; Synovitis; T-Lymphocytes; Treatment Outcome; Uveitis | 2013 |
The protean ocular involvement in monogenic autoinflammatory diseases: state of the art.
Topics: Arthritis; Autoimmune Diseases; Cryopyrin-Associated Periodic Syndromes; Cytokines; Eye Diseases; Familial Mediterranean Fever; Female; Fever; Hereditary Autoinflammatory Diseases; Humans; Inflammation; Interleukin-1beta; Male; Mevalonate Kinase Deficiency; Mutation; Phosphotransferases (Alcohol Group Acceptor); Sarcoidosis; Synovitis; Uveitis | 2015 |
Monogenic Auto-inflammatory Syndromes: A Review of the Literature.
Topics: Acne Vulgaris; Antirheumatic Agents; Arthritis; Arthritis, Infectious; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Infliximab; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Macrophages; Mevalonate Kinase Deficiency; Monocytes; Pyoderma Gangrenosum; Sarcoidosis; Synovitis; Uveitis | 2016 |
Inflammasome-mediated autoinflammatory disorders.
Topics: Adaptor Proteins, Signal Transducing; Apoptosis Regulatory Proteins; Arthritis; Asbestosis; Carrier Proteins; Crohn Disease; Cryopyrin-Associated Periodic Syndromes; Diabetes Mellitus; Familial Mediterranean Fever; Humans; Immunity, Innate; Intracellular Signaling Peptides and Proteins; Mutation; NLR Family, Pyrin Domain-Containing 3 Protein; NLR Proteins; Nod2 Signaling Adaptor Protein; Receptors, Interleukin-1; Silicosis; Vitiligo | 2010 |
Nucleotide-binding oligomerization domain-like receptors and inflammasomes in the pathogenesis of non-microbial inflammation and diseases.
Topics: Animals; Arthritis; Atherosclerosis; Cryopyrin-Associated Periodic Syndromes; Diabetes Mellitus; Humans; Inflammasomes; Inflammation; Inflammation Mediators; Interleukin-18; Interleukin-1beta; Myocardial Infarction; Neurodegenerative Diseases; Obesity; Protein Structure, Tertiary; Receptors, Cell Surface | 2012 |
NOMID: the radiographic and MRI features and review of literature.
Topics: Ankle Joint; Arthritis; Child; Cryopyrin-Associated Periodic Syndromes; Exanthema; Humans; Knee Joint; Magnetic Resonance Imaging; Male; Radiography | 2012 |
6 other study(ies) available for trolamine salicylate and Chronic Infantile Neurologic, Cutaneous, and Articular Syndrome
| Article | Year |
|---|---|
Contrasting role of
Topics: Animals; Arthritis; Cryopyrin-Associated Periodic Syndromes; Female; Humans; Intracellular Signaling Peptides and Proteins; Mice; Mutation, Missense; Phenotype | 2021 |
Pattern and diagnostic evaluation of systemic autoinflammatory diseases other than familial Mediterranean fever among Arab children: a multicenter study from the Pediatric Rheumatology Arab Group (PRAG).
Topics: Acne Vulgaris; Adolescent; Anemia, Dyserythropoietic, Congenital; Antirheumatic Agents; Arabs; Arthritis; Arthritis, Infectious; Arthritis, Juvenile; Bahrain; Child; Child, Preschool; Consanguinity; Crohn Disease; Cross-Sectional Studies; Cryopyrin-Associated Periodic Syndromes; Diagnostic Errors; Female; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunologic Deficiency Syndromes; Infant; Intracellular Signaling Peptides and Proteins; Jordan; Kuwait; Libya; Male; Mevalonate Kinase Deficiency; Oman; Osteomyelitis; Pyoderma Gangrenosum; Retrospective Studies; Sarcoidosis; Saudi Arabia; Synovitis; United Arab Emirates; Uveitis | 2020 |
Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry.
Topics: Adolescent; Adult; Alleles; Arthralgia; Arthritis; Carrier Proteins; Child; Child, Preschool; Cohort Studies; Conjunctivitis; Cryopyrin-Associated Periodic Syndromes; Europe; Exanthema; Female; Genotype; Germ-Line Mutation; Headache; Hearing Loss, Sensorineural; Heterozygote; Humans; Infant; Male; Meningitis; Mutation; Myalgia; NLR Family, Pyrin Domain-Containing 3 Protein; Papilledema; Phenotype; Registries; Retrospective Studies; Severity of Illness Index; Uveitis; Young Adult | 2015 |
Musculoskeletal symptoms in patients with cryopyrin-associated periodic syndromes: a large database study.
Topics: Adolescent; Adult; Aged; Arthralgia; Arthritis; Child; Child, Preschool; Cryopyrin-Associated Periodic Syndromes; Databases, Factual; Female; Humans; Infant; Infant, Newborn; Male; Middle Aged; Musculoskeletal System; Mutation; Myalgia; Phenotype; Young Adult | 2015 |
NLRP3 A439V Mutation in a Large Family with Cryopyrin-associated Periodic Syndrome: Description of Ophthalmologic Symptoms in Correlation with Other Organ Symptoms.
Topics: Adolescent; Adult; Aged; Arthralgia; Arthritis; Child; Conjunctivitis; Cryopyrin-Associated Periodic Syndromes; Female; Humans; Male; Middle Aged; Mutation; NLR Family, Pyrin Domain-Containing 3 Protein; Pedigree; Phenotype; Retrospective Studies; Uveitis; Young Adult | 2016 |
Muckle-Wells syndrome in Chinese patients: a single center case series.
Topics: Adolescent; Adult; Arthritis; Asian People; China; Cryopyrin-Associated Periodic Syndromes; Exanthema; Heterozygote; Humans; Male; Middle Aged; Mutation; NLR Family, Pyrin Domain-Containing 3 Protein; Oral Ulcer; Phenotype; Young Adult | 2017 |