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2012 1
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Page 1
Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents.
Hospach T, Glowatzki F, Blankenburg F, Conzelmann D, Stirnkorb C, Müllerschön CS, von den Driesch P, Köhler LM, Rohlfs M, Klein C, Hauck F. Hospach T, et al. Pediatr Rheumatol Online J. 2019 Jul 8;17(1):37. doi: 10.1186/s12969-019-0338-1. Pediatr Rheumatol Online J. 2019. PMID: 31286990 Free PMC article. Review.
BACKGROUND: Deficiency of interleukin-36 receptor antagonist (DITRA) is a life threatening monogenic autoinflammatory disease caused by loss of function mutations in the IL36RN gene. ...
BACKGROUND: Deficiency of interleukin-36 receptor antagonist (DITRA) is a life threatening monogenic auto …
Cutaneous findings and treatments in deficiency of interleukin-36 receptor antagonist (DITRA): A review of the literature.
Okorie CL, Nayudu K, Nambudiri VE. Okorie CL, et al. Exp Dermatol. 2024 Jan;33(1):e14934. doi: 10.1111/exd.14934. Epub 2023 Sep 19. Exp Dermatol. 2024. PMID: 37726967 Review.
Deficiency of the interleukin-36 receptor antagonist (DITRA) is a rare autoinflammatory disorder caused by mutations in the IL36RN gene. This mutation leads to a lack of functional interleukin-36 receptor antagonists …
Deficiency of the interleukin-36 receptor antagonist (DITRA) is a rare autoinflammatory disorder caused b …
Role of Interleukin-36 in inflammatory joint diseases.
Wang C, Hu J, Shi J. Wang C, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Apr 25;52(2):249-259. doi: 10.3724/zdxbyxb-2023-0034. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 37283111 Free PMC article. Review. Chinese, English.
Interleukin (IL)-36 is a family of cytokines that belongs to the larger IL-1 superfamily. IL-36 agonist/antagonist binds to the interleukin-36 receptor involving in physiological inflammation regulation and pathogenesis of many inflammatory diseases. . …
Interleukin (IL)-36 is a family of cytokines that belongs to the larger IL-1 superfamily. IL-36 agonist/antagonist binds to the in …
The emergence of the IL-36 cytokine family as novel targets for inflammatory diseases.
Walsh PT, Fallon PG. Walsh PT, et al. Ann N Y Acad Sci. 2018 Apr;1417(1):23-34. doi: 10.1111/nyas.13280. Epub 2016 Oct 26. Ann N Y Acad Sci. 2018. PMID: 27783881 Review.
The IL-36 subfamily consists of three ligands-IL-36alpha, IL-36beta, and IL-36gamma-and the natural antagonist IL-36Ra. The cytokines exert their effects through a specific IL-36 receptor consisting of IL-36R and IL-1RAcP chains. ...In humans, inactivating mutations …
The IL-36 subfamily consists of three ligands-IL-36alpha, IL-36beta, and IL-36gamma-and the natural antagonist IL-36Ra. The cytokines …
Autoinflammatory diseases in pediatrics.
Hausmann JS, Dedeoglu F. Hausmann JS, et al. Dermatol Clin. 2013 Jul;31(3):481-94. doi: 10.1016/j.det.2013.04.003. Epub 2013 Jun 2. Dermatol Clin. 2013. PMID: 23827250 Review.
It discusses pharyngitis, and cervical adenitis and the monogenic autoinflammatory diseases that cause recurrent fevers including familial Mediterranean fever, hyper-immunoglobulin (Ig) D and periodic fever syndrome, tumor necrosis factor receptor-associated periodic syndr …
It discusses pharyngitis, and cervical adenitis and the monogenic autoinflammatory diseases that cause recurrent fevers including familial M …
Autoinflammatory pustular neutrophilic diseases.
Naik HB, Cowen EW. Naik HB, et al. Dermatol Clin. 2013 Jul;31(3):405-25. doi: 10.1016/j.det.2013.04.001. Epub 2013 Jun 2. Dermatol Clin. 2013. PMID: 23827244 Free PMC article. Review.
Monogenic diseases with pustular phenotypes are discussed, including deficiency of interleukin 1 receptor antagonist, deficiency of the interleukin 36 receptor antagonist, CARD14-associated pustular psoriasis, and pyogenic a …
Monogenic diseases with pustular phenotypes are discussed, including deficiency of interleukin 1 receptor antagonist, …
Designation of Autoinflammatory Skin Manifestations With Specific Genetic Backgrounds.
Kanazawa N. Kanazawa N. Front Immunol. 2020 Mar 18;11:475. doi: 10.3389/fimmu.2020.00475. eCollection 2020. Front Immunol. 2020. PMID: 32256502 Free PMC article. Review.
"Autoinflammatory disease (AiD)" has first been introduced in 1999 when the responsible gene for the familial Hibernean fever or autosomal dominant-type familial Mediterranean fever-like periodic fever syndrome was reportedly identified as tumor necrosis factor receptor su …
"Autoinflammatory disease (AiD)" has first been introduced in 1999 when the responsible gene for the familial Hibernean fever or autosomal d …
Monogenic autoinflammatory diseases: concept and clinical manifestations.
Almeida de Jesus A, Goldbach-Mansky R. Almeida de Jesus A, et al. Clin Immunol. 2013 Jun;147(3):155-74. doi: 10.1016/j.clim.2013.03.016. Epub 2013 Apr 9. Clin Immunol. 2013. PMID: 23711932 Free PMC article. Review.
The autoinflammatory diseases can be grouped based on clinical findings: 1. the three classic hereditary "periodic fever syndromes", familial Mediterranean Fever (FMF); TNF receptor associated periodic syndrome (TRAPS); and mevalonate kinase deficiency/hyperimmunogl …
The autoinflammatory diseases can be grouped based on clinical findings: 1. the three classic hereditary "periodic fever syndromes", familia …
Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways.
Kanazawa N. Kanazawa N. J Dermatol Sci. 2012 Jun;66(3):183-9. doi: 10.1016/j.jdermsci.2012.01.004. Epub 2012 Jan 18. J Dermatol Sci. 2012. PMID: 22336993 Review.
In this review, three categories of autoinflammatory disorders are discussed: inflammasomopathies, receptor antagonist deficiencies and proteasome disability syndromes. ...Analyses of these diseases have clarified some critical pathways regulating NLRP3 infla …
In this review, three categories of autoinflammatory disorders are discussed: inflammasomopathies, receptor antagonist defi …
11 results