Page last updated: 2024-08-22

trolamine salicylate and Hereditary Autoinflammation Diseases

trolamine salicylate has been researched along with Hereditary Autoinflammation Diseases in 23 studies

Research

Studies (23)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (4.35)29.6817
2010's16 (69.57)24.3611
2020's6 (26.09)2.80

Authors

AuthorsStudies
Brunetta, E; Folci, M; Nasone, I; Rodolfi, S; Selmi, C1
Ayaz, NA; Çakan, M; Çakmak, F; Demir, F; Karadağ, ŞG; Sönmez, HE; Sözeri, B; Tanatar, A1
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, M1
Bonnekoh, H; Butze, M; Kallinich, T; Kambe, N; Kokolakis, G; Krause, K1
Kosmider, O; Lacombe, V; Lavigne, C; Prévost, M; Urbanski, G1
Barba, T; Bourbon, E; Durel, CA; Hot, A; Jamilloux, Y; Mestrallet, F; Sujobert, P1
Abdollahi-Roodsaz, S; Boekhorst, J; Ederveen, THA; Frambach, SJCM; Garssen, J; Knol, J; Koenders, MI; Manasson, J; Rogier, R; Scher, JU; van den Berg, WB; van der Kraan, PM; van Hijum, SAFT; Wopereis, H1
Ankli, B; Daikeler, T; Khanlari, B; Pegios, V; Zettl, A1
Carlomagno, R; Hentgen, V1
Brizi, MG; Cantarini, L; Caso, F; Galeazzi, M; Guerrini, S; Lucherini, OM; Magnotti, F; Muscari, I; Patti, M; Punzi, L; Rigante, D; Vitale, A1
Eguchi, K; Migita, K; Nonaka, F1
Federici, S; Gattorno, M1
Bertin, J; Foley, KP; Maes, A; Rose, CD; Wouters, CH1
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, L1
Blank, N; Hegenbart, U; Schönland, S1
Ben-Chetrit, E; Peleg, H1
Afraei, S; Azizi, G; Ghiasy, S; Khadem Azarian, S; Khan Nazer, NH; Mirshafiey, A; Mohebi, A; Mosayebian, A; Nazeri, S; Sadri, G1
Barbosa, CM; Hilário, MO; Len, CA; Matos, TC; Petry, DG; Terreri, MT1
Bendtzen, K1
Aosai, F; Iwakura, Y; Moroda, M; Washino, T1
Feldmeyer, L1
Caso, F; Galozzi, P; Gava, A; Punzi, L; Sfriso, P; Tognon, S1
Soubrier, M; Tatar, Z; Vayssade, M1

Reviews

10 review(s) available for trolamine salicylate and Hereditary Autoinflammation Diseases

ArticleYear
Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms.
    Acta dermato-venereologica, 2020, Mar-25, Volume: 100, Issue:7

    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.
    Mediators of inflammation, 2013, Volume: 2013

    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
A practical approach to the diagnosis of autoinflammatory diseases in childhood.
    Best practice & research. Clinical rheumatology, 2014, Volume: 28, Issue:2

    Topics: Arthritis; Child; Chronic Disease; Diagnosis, Differential; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Mutation; Syndrome

2014
Blau syndrome, the prototypic auto-inflammatory granulomatous disease.
    Pediatric rheumatology online journal, 2014, Volume: 12

    Topics: Arthritis; Cranial Nerve Diseases; Dermatitis; Granuloma; Hereditary Autoinflammatory Diseases; Humans; Mutation; Nod2 Signaling Adaptor Protein; Prospective Studies; Sarcoidosis; Signal Transduction; Synovitis; Uveitis

2014
The protean ocular involvement in monogenic autoinflammatory diseases: state of the art.
    Clinical rheumatology, 2015, Volume: 34, Issue:7

    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
[Causes and treatment of systemic amyloidosis].
    Zeitschrift fur Rheumatologie, 2016, Volume: 75, Issue:2

    Topics: Amyloidosis; Arthritis; Cohort Studies; Evidence-Based Medicine; Hereditary Autoinflammatory Diseases; Humans; Inflammatory Bowel Diseases; Kidney Diseases; Lung Diseases; Rare Diseases; Treatment Outcome

2016
Vasculitis in the autoinflammatory diseases.
    Current opinion in rheumatology, 2017, Volume: 29, Issue:1

    Topics: Arthritis; Autoimmune Diseases; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; IgA Vasculitis; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Pyoderma Gangrenosum; Sarcoidosis; Skin Diseases; Synovitis; Uveitis; Vasculitis

2017
Monogenic Auto-inflammatory Syndromes: A Review of the Literature.
    Iranian journal of allergy, asthma, and immunology, 2016, Volume: 15, Issue:6

    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
Blau syndrome, clinical and genetic aspects.
    Autoimmunity reviews, 2012, Volume: 12, Issue:1

    Topics: Arthritis; Cranial Nerve Diseases; Hereditary Autoinflammatory Diseases; Humans; Nod2 Signaling Adaptor Protein; Sarcoidosis; Synovitis; Uveitis

2012
[Palindromic rheumatism].
    La Revue de medecine interne, 2013, Volume: 34, Issue:1

    Topics: Arthritis; Arthritis, Rheumatoid; Citrulline; Cytoskeletal Proteins; Diagnosis, Differential; Disease Progression; Hereditary Autoinflammatory Diseases; Humans; Mutation; Pyrin; Rheumatic Diseases; Rheumatoid Factor

2013

Other Studies

13 other study(ies) available for trolamine salicylate and Hereditary Autoinflammation Diseases

ArticleYear
Autoinflammatory manifestations in adult patients.
    Clinical and experimental immunology, 2022, 12-31, Volume: 210, Issue:3

    Topics: Adult; Arthritis; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Inflammasomes; Interleukin-1

2022
Performance of Tel-Hashomer, Livneh, pediatric and new Eurofever/PRINTO classification criteria for familial Mediterranean fever in a referral center.
    Rheumatology international, 2020, Volume: 40, Issue:1

    Topics: Adolescent; Arthritis; Case-Control Studies; Chest Pain; Child; Child, Preschool; Colchicine; Consanguinity; Drug Resistance; Exons; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Heterozygote; Homozygote; Humans; Male; Mutation; Pyrin; Reproducibility of Results; Retrospective Studies; Severity of Illness Index; Tubulin Modulators

2020
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).
    Rheumatology international, 2020, Volume: 40, Issue:1

    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
Severe Joint Involvement in VEXAS Syndrome: A Case Report.
    Annals of internal medicine, 2021, Volume: 174, Issue:7

    Topics: Aged; Anemia, Macrocytic; Arthritis; Bone Marrow Examination; Cartilage Diseases; Genes, X-Linked; Hereditary Autoinflammatory Diseases; Humans; Male; Skin Diseases; Syndrome; Ubiquitin-Activating Enzymes; Venous Thromboembolism

2021
VEXAS syndrome in a woman.
    Rheumatology (Oxford, England), 2021, 11-03, Volume: 60, Issue:11

    Topics: Acute-Phase Proteins; Anemia, Macrocytic; Arthritis; Diagnosis, Differential; Female; Hearing Loss, Sensorineural; Hereditary Autoinflammatory Diseases; Humans; Middle Aged; Mutation; Myelodysplastic Syndromes; Myeloid Progenitor Cells; Scleritis; Symptom Assessment; Ubiquitin-Activating Enzymes; Vacuoles

2021
Aberrant intestinal microbiota due to IL-1 receptor antagonist deficiency promotes IL-17- and TLR4-dependent arthritis.
    Microbiome, 2017, 06-23, Volume: 5, Issue:1

    Topics: Animals; Anti-Bacterial Agents; Arthritis; Autoimmune Diseases; Gastrointestinal Microbiome; Genetic Variation; Helicobacter; Hereditary Autoinflammatory Diseases; High-Throughput Nucleotide Sequencing; Interleukin 1 Receptor Antagonist Protein; Interleukin-17; Intestinal Mucosa; Mice; Mice, Knockout; Mucous Membrane; Prevotella; RNA, Ribosomal, 16S; Ruminococcus; Th17 Cells; Toll-Like Receptor 4

2017
Whipple's disease mimicking an auto-inflammatory disease with myositis and soft tissue inflammation.
    Joint bone spine, 2018, Volume: 85, Issue:5

    Topics: Aged; Arthritis; Biopsy, Needle; Diagnosis, Differential; Female; Hereditary Autoinflammatory Diseases; Humans; Immunohistochemistry; Myositis; Risk Assessment; Soft Tissue Infections; Thigh; Whipple Disease

2018
[Recurrent auto-inflammatory fevers : a practical diagnostic flow chart].
    Revue medicale suisse, 2018, Feb-14, Volume: 14, Issue:594

    Topics: Arthritis; Child; Fever; Hereditary Autoinflammatory Diseases; Humans; Inflammation; Syndrome

2018
[Autoinflammatory diseases reach adolescence].
    Arerugi = [Allergy], 2013, Volume: 62, Issue:8

    Topics: Adolescent; Arthritis; Cranial Nerve Diseases; Erythema Nodosum; Familial Mediterranean Fever; Fever; Fingers; Hereditary Autoinflammatory Diseases; Humans; Sarcoidosis; Synovitis; Uveitis

2013
Autoinflammatory syndromes: report on three cases.
    Sao Paulo medical journal = Revista paulista de medicina, 2009, Volume: 127, Issue:5

    Topics: Adult; Arthritis; Arthritis, Juvenile; Child; Diagnosis, Differential; Fatal Outcome; Female; Fever; Genetic Testing; Hereditary Autoinflammatory Diseases; Humans; Male; Recurrence; Syndrome; Young Adult

2009
[Danger signals and inflammasomes in autoinflammatory and autoimmune diseases].
    Ugeskrift for laeger, 2011, Sep-19, Volume: 173, Issue:38

    Topics: Arteriosclerosis; Arthritis; Autoimmune Diseases; Cytokines; Diabetes Mellitus, Type 1; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Inflammasomes; Inflammation; Nod Signaling Adaptor Proteins; Receptors, Pattern Recognition; Receptors, Tumor Necrosis Factor; Toll-Like Receptors

2011
Toxoplasma gondii infection inhibits Th17-mediated spontaneous development of arthritis in interleukin-1 receptor antagonist-deficient mice.
    Infection and immunity, 2012, Volume: 80, Issue:4

    Topics: Animals; Arthritis; CD11c Antigen; CD4-Positive T-Lymphocytes; GATA3 Transcription Factor; Hereditary Autoinflammatory Diseases; Interferon-gamma; Interleukin 1 Receptor Antagonist Protein; Interleukin-10; Interleukin-12 Subunit p40; Interleukin-17; Interleukin-1beta; Interleukin-4; Interleukin-6; Lymph Nodes; Mice; Mice, Inbred BALB C; Mice, Knockout; Nuclear Receptor Subfamily 1, Group F, Member 3; RNA, Messenger; Spleen; Th1 Cells; Th17 Cells; Th2 Cells; Toxoplasma; Toxoplasmosis

2012
[Autoinflammatory syndromes in dermatology].
    Revue medicale suisse, 2012, Apr-04, Volume: 8, Issue:335

    Topics: Arthritis; Cranial Nerve Diseases; Hereditary Autoinflammatory Diseases; Humans; Receptors, Interleukin-1 Type I; Sarcoidosis; Schnitzler Syndrome; Skin Diseases; Still's Disease, Adult-Onset; Synovitis; Uveitis

2012