trolamine salicylate has been researched along with Panuveitis in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (40.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Asano, N; Eishi, Y; Hasegawa, S; Honda, Y; Hoshii, Y; Izawa, K; Korenaga, Y; Nakamura, T; Nishikomori, R; Ohga, S; Okazaki, F; Tanabe, T; Uchi, S; Uchida, K; Wakiguchi, H; Yanai, R; Yasudo, H | 1 |
Achille, M; Gabriele, S; Ilaria, P; Ilir, A; Piergiorgio, N; Roberto, C; Rolando, C; Teresa, G | 1 |
Jung, LK; Miller, MM; Raiji, VR | 1 |
Becker, ML; Rose, CD | 1 |
Bless, D; Daikeler, T; Koitschev, A; Kötter, I; Schlote, T; Stübiger, N; Zierhut, M | 1 |
1 review(s) available for trolamine salicylate and Panuveitis
Article | Year |
---|---|
Blau syndrome and related genetic disorders causing childhood arthritis.
Topics: Adolescent; Age of Onset; Arthritis; Arthritis, Juvenile; Biopsy, Needle; Child; Exanthema; Female; Granuloma; Humans; Immunohistochemistry; Intracellular Signaling Peptides and Proteins; Male; Nod2 Signaling Adaptor Protein; Panuveitis; Prognosis; Risk Assessment; Sensitivity and Specificity; Syndrome | 2005 |
4 other study(ies) available for trolamine salicylate and Panuveitis
Article | Year |
---|---|
A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes.
Topics: Antirheumatic Agents; Arthritis; Biopsy; Child; Dermatitis; Female; Granuloma; Humans; Immunohistochemistry; Methotrexate; Mutation; Nod2 Signaling Adaptor Protein; Panuveitis; Prednisolone; Propionibacterium acnes; Sarcoidosis; Skin; Synovitis; Treatment Outcome; Uveitis | 2021 |
Successful treatment with adalimumab for severe multifocal choroiditis and panuveitis in presumed (early-onset) ocular sarcoidosis.
Topics: Adalimumab; Anti-Inflammatory Agents; Arthritis; Child; Choroiditis; Female; Humans; Panuveitis; Sarcoidosis; Synovitis; Treatment Outcome; Uveitis | 2016 |
Uveitis in Blau syndrome from a de novo mutation of the NOD2/CARD15 gene.
Topics: Arthritis; Child, Preschool; Chromosomes, Human, Pair 16; Cranial Nerve Diseases; Female; Humans; Immunosuppressive Agents; Nod2 Signaling Adaptor Protein; Panuveitis; Point Mutation; Sarcoidosis; Synovitis; Uveitis; Visual Acuity | 2011 |
[Cogan I syndrome: clinical aspects, therapy and prognosis].
Topics: Adolescent; Adrenal Cortex Hormones; Adult; Aged; Arthritis; Cataract; Deafness; Female; Humans; Immunosuppressive Agents; Keratitis; Male; Middle Aged; Panuveitis; Pericarditis; Prognosis; Retrospective Studies; Scleritis; Syndrome; Time Factors; Tinnitus; Uveitis, Anterior; Uveitis, Posterior | 2000 |