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Year Number of Results
2002 1
2005 1
2006 2
2007 4
2008 5
2009 3
2010 4
2011 4
2012 5
2013 13
2014 12
2015 6
2016 5
2017 8
2018 14
2019 14
2020 17
2021 14
2022 16
2023 17
2024 9

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151 results

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Page 1
An update on VEXAS syndrome.
Al-Hakim A, Savic S. Al-Hakim A, et al. Expert Rev Clin Immunol. 2023 Feb;19(2):203-215. doi: 10.1080/1744666X.2023.2157262. Epub 2022 Dec 26. Expert Rev Clin Immunol. 2023. PMID: 36537591 Free article. Review.
INTRODUCTION: VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a recently described, late-onset, acquired autoinflammatory disorder caused by mutations in the UBA1 gene. The various clinical manifestations of VEXAS broadly divided into in …
INTRODUCTION: VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a recently described, late-onset, acquired aut …
Pyoderma gangrenosum.
Maverakis E, Marzano AV, Le ST, Callen JP, Brüggen MC, Guenova E, Dissemond J, Shinkai K, Langan SM. Maverakis E, et al. Nat Rev Dis Primers. 2020 Oct 8;6(1):81. doi: 10.1038/s41572-020-0213-x. Nat Rev Dis Primers. 2020. PMID: 33033263 Review.
The cause of PG is not well understood, but PG is generally considered an autoinflammatory disorder. Studies have focused on the role of T cells, especially at the wound margin; these cells may support the destructive autoinflammatory response by the innate immune s …
The cause of PG is not well understood, but PG is generally considered an autoinflammatory disorder. Studies have focused on t …
Adult-onset Still's disease.
Gerfaud-Valentin M, Jamilloux Y, Iwaz J, Sève P. Gerfaud-Valentin M, et al. Autoimmun Rev. 2014 Jul;13(7):708-22. doi: 10.1016/j.autrev.2014.01.058. Epub 2014 Mar 19. Autoimmun Rev. 2014. PMID: 24657513 Free article. Review.
Chronic recurrent multifocal osteomyelitis. A narrative and pictorial review.
Sergi CM, Miller E, Demellawy DE, Shen F, Zhang M. Sergi CM, et al. Front Immunol. 2022 Aug 22;13:959575. doi: 10.3389/fimmu.2022.959575. eCollection 2022. Front Immunol. 2022. PMID: 36072576 Free PMC article. Review.
Chronic recurrent and multifocal osteomyelitis (CRMO) is a nonsporadic autoinflammatory disorder. Currently, it is diagnosed based on clinical, radiologic, pathological, and longitudinal data. ...
Chronic recurrent and multifocal osteomyelitis (CRMO) is a nonsporadic autoinflammatory disorder. Currently, it is diagnosed b …
NLRP3 inflammasome and NLRP3-related autoinflammatory diseases: From cryopyrin function to targeted therapies.
Moltrasio C, Romagnuolo M, Marzano AV. Moltrasio C, et al. Front Immunol. 2022 Oct 6;13:1007705. doi: 10.3389/fimmu.2022.1007705. eCollection 2022. Front Immunol. 2022. PMID: 36275641 Free PMC article. Review.
Cryopyrin associated periodic syndrome (CAPS) is a rare inherited autoinflammatory disorder, clinically characterized by cutaneous and systemic, musculoskeletal, and central nervous system inflammation. ...
Cryopyrin associated periodic syndrome (CAPS) is a rare inherited autoinflammatory disorder, clinically characterized by cutan …
Tumor necrosis factor-associated periodic syndrome in adults.
Menon SG, Efthimiou P. Menon SG, et al. Rheumatol Int. 2018 Jan;38(1):3-11. doi: 10.1007/s00296-017-3820-4. Epub 2017 Sep 23. Rheumatol Int. 2018. PMID: 28942479 Review.
Tumor necrosis factor-associated periodic syndrome is an autoinflammatory disorder classified under hereditary periodic fever syndromes. ...
Tumor necrosis factor-associated periodic syndrome is an autoinflammatory disorder classified under hereditary periodic fever …
A Cohort Study on Deficiency of ADA2 from China.
Li GM, Han X, Wu Y, Wang W, Tang HX, Lu MP, Tang XM, Lin Y, Deng F, Yang J, Wang XN, Liu CC, Zheng WJ, Wu BB, Zhou F, Luo H, Zhang L, Liu HM, Guan WZ, Wang SH, Tao PF, Jin TJ, Fang R, Wu Y, Zhang J, Zhang Y, Zhang TN, Yin W, Guo L, Tang WJ, Chang H, Zhang QY, Li XZ, Li JG, Zhou ZX, Yang SR, Yang KK, Xu H, Song HM, Deuitch NT, Lee PY, Zhou Q, Sun L. Li GM, et al. J Clin Immunol. 2023 May;43(4):835-845. doi: 10.1007/s10875-023-01432-8. Epub 2023 Feb 18. J Clin Immunol. 2023. PMID: 36807221 Free PMC article.
PURPOSE: Deficiency of adenosine deaminase 2 (DADA2), an autosomal recessive autoinflammatory disorder caused by biallelic loss-of-function variants in adenosine deaminase 2 (ADA2), has not been systemically investigated in Chinese population yet. ...
PURPOSE: Deficiency of adenosine deaminase 2 (DADA2), an autosomal recessive autoinflammatory disorder caused by biallelic los …
Systemic Juvenile Idiopathic Arthritis: Diagnosis and Management.
Kumar S. Kumar S. Indian J Pediatr. 2016 Apr;83(4):322-7. doi: 10.1007/s12098-016-2060-z. Epub 2016 Feb 26. Indian J Pediatr. 2016. PMID: 26916892 Review.
In sJIA, systemic inflammation has been associated with dysregulation of the innate immune system, suggesting that it is an autoinflammatory disorder. IL-1 and IL-6 play a major role in the pathogenesis of sJIA and treatment with IL-1 and IL-6 inhibitors has shown t …
In sJIA, systemic inflammation has been associated with dysregulation of the innate immune system, suggesting that it is an autoinflammat …
Adult-onset Still's disease as a cutaneous marker of systemic disease.
Damevska K, França K, Nikolovska S, Gucev F. Damevska K, et al. Clin Dermatol. 2019 Nov-Dec;37(6):668-674. doi: 10.1016/j.clindermatol.2019.07.034. Epub 2019 Aug 1. Clin Dermatol. 2019. PMID: 31864446 Review.
The disease has been recently classified as a polygenic autoinflammatory disorder at the "crossroads" of autoinflammatory and autoimmune diseases. ...
The disease has been recently classified as a polygenic autoinflammatory disorder at the "crossroads" of autoinflammatory and …
151 results