trolamine salicylate has been researched along with Hyper IgD Syndrome in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 5 (55.56) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| 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 |
| 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 |
| 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 |
| Afraei, S; Azizi, G; Ghiasy, S; Khadem Azarian, S; Khan Nazer, NH; Mirshafiey, A; Mohebi, A; Mosayebian, A; Nazeri, S; Sadri, G | 1 |
| Caroli, F; Ceccherini, I; Martini, G; Meneghesso, D; Zulian, F | 1 |
| Anikster, Y; Kleid, D; Megged, O; Navon-Elkan, P | 1 |
| Daragon, A; Klemmer, N; Le Loët, X; Lequerré, T; Mejjad, O; Pouplin, S; Prieur, AM; Vittecoq, O | 1 |
| Aksentijevich, I; Farasat, S; Toro, JR | 1 |
4 review(s) available for trolamine salicylate and Hyper IgD Syndrome
| Article | Year |
|---|---|
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 |
Autoinflammatory diseases: clinical and genetic advances.
Topics: Arthritis; Autoimmune Diseases; Familial Mediterranean Fever; Humans; Mevalonate Kinase Deficiency; Pyoderma Gangrenosum; Receptors, Tumor Necrosis Factor; Urticaria | 2008 |
5 other study(ies) available for trolamine salicylate and Hyper IgD Syndrome
| Article | Year |
|---|---|
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 |
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 |
Recurrent arthritis as a unique manifestation of hyperimmunoglobulinaemia D.
Topics: Abdominal Pain; Arthritis; Child, Preschool; Diagnosis, Differential; Female; Fever; Humans; Mevalonate Kinase Deficiency; Recurrence | 2009 |
Recurrent Fever, arthritis, lymphadenopathy, and hepatosplenomegaly.
Topics: Arthritis; Child; Female; Fever; Humans; Lymphatic Diseases; Mevalonate Kinase Deficiency; Recurrence | 2011 |
Mevalonate kinase deficiency syndrome with structural damage responsive to anakinra.
Topics: Adult; Arthritis; Dose-Response Relationship, Drug; Drug Administration Schedule; Female; Follow-Up Studies; Humans; Interleukin 1 Receptor Antagonist Protein; Mevalonate Kinase Deficiency; Pain Measurement; Recovery of Function; Treatment Outcome | 2007 |