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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2001 1
2002 2
2003 5
2004 1
2005 3
2006 4
2007 9
2008 2
2009 5
2010 1
2011 5
2012 5
2013 5
2014 6
2015 5
2016 3
2017 7
2018 3
2019 5
2020 8
2021 7
2022 2
2023 2

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87 results

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Page 1
Periodic fever syndromes.
Lachmann HJ. Lachmann HJ. Best Pract Res Clin Rheumatol. 2017 Aug;31(4):596-609. doi: 10.1016/j.berh.2017.12.001. Epub 2018 Jan 11. Best Pract Res Clin Rheumatol. 2017. PMID: 29773275 Review.
Progress in the genetics of uveitis.
Huang XF, Brown MA. Huang XF, et al. Genes Immun. 2022 Apr;23(2):57-65. doi: 10.1038/s41435-022-00168-6. Epub 2022 Apr 4. Genes Immun. 2022. PMID: 35379982 Free PMC article. Review.
In addition, a few monogenic autoinflammatory disorders can also cause uveitis, such as Blau Syndrome and haploinsufficiency of A20 (HA20). Although the exact pathogenesis of non-infectious uveitis is still unclear, it is well-recognised that it involves both geneti …
In addition, a few monogenic autoinflammatory disorders can also cause uveitis, such as Blau Syndrome and haploinsufficiency o …
Blau syndrome revisited.
Rose CD, Martin TM, Wouters CH. Rose CD, et al. Curr Opin Rheumatol. 2011 Sep;23(5):411-8. doi: 10.1097/BOR.0b013e328349c430. Curr Opin Rheumatol. 2011. PMID: 21788900 Review.
PURPOSE OF REVIEW: Blau syndrome is a monogenic disease resulting from mutations in nucleotide oligomerization domain 2 (NOD2) and is phenotypically characterized by granulomatous polyarthritis and uveitis. ...A brief review of more recent advances in relevant pathw …
PURPOSE OF REVIEW: Blau syndrome is a monogenic disease resulting from mutations in nucleotide oligomerization domain 2 (NOD2) …
Ocular manifestations of Blau syndrome.
Suresh S, Tsui E. Suresh S, et al. Curr Opin Ophthalmol. 2020 Nov;31(6):532-537. doi: 10.1097/ICU.0000000000000705. Curr Opin Ophthalmol. 2020. PMID: 33009086 Review.
PURPOSE OF REVIEW: This article summarizes the systemic and ocular manifestations of Blau syndrome, its genetic basis, and reviews recently published literature. ...Case reports have demonstrated the successful use of newer biologic agents. SUMMARY: Blau s …
PURPOSE OF REVIEW: This article summarizes the systemic and ocular manifestations of Blau syndrome, its genetic basis, and rev …
Distinguishing Blau Syndrome from Systemic Sarcoidosis.
Kaufman KP, Becker ML. Kaufman KP, et al. Curr Allergy Asthma Rep. 2021 Feb 9;21(2):10. doi: 10.1007/s11882-021-00991-3. Curr Allergy Asthma Rep. 2021. PMID: 33560445 Free PMC article. Review.
PURPOSE OF REVIEW: The purpose of this review is to provide a framework to distinguish Blau syndrome/Early Onset Sarcoidosis and Sarcoidosis clinically. ...Blau syndrome and Early Onset Sarcoidosis are due to one of numerous possible gain-of-function m …
PURPOSE OF REVIEW: The purpose of this review is to provide a framework to distinguish Blau syndrome/Early Onset Sarcoidosis a …
Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis.
Takada S, Saito MK, Kambe N. Takada S, et al. G Ital Dermatol Venereol. 2020 Oct;155(5):537-541. doi: 10.23736/S0392-0488.19.06524-6. Epub 2020 Jul 2. G Ital Dermatol Venereol. 2020. PMID: 32618442 Review.
Blau Syndrome, or early-onset sarcoidosis, is hereditary juvenile-onset systemic granulomatosis. ...Although tumor necrosis factor alpha (TNFalpha) antagonists are effective for controlling some of the symptoms of Blau Syndrome, there is no specific cu …
Blau Syndrome, or early-onset sarcoidosis, is hereditary juvenile-onset systemic granulomatosis. ...Although tumor necrosis fa …
Vasculitis in the autoinflammatory diseases.
Peleg H, Ben-Chetrit E. Peleg H, et al. Curr Opin Rheumatol. 2017 Jan;29(1):4-11. doi: 10.1097/BOR.0000000000000347. Curr Opin Rheumatol. 2017. PMID: 27755121 Review.
It is rarely described in hyper IgD with periodic fever syndrome, cryopyrin associated periodic syndromes, TNF receptor-associated periodic syndrome, deficiency of interleukin-1 receptor antagonist and pyoderma gangrenosum and acne syndrome. In most AID where …
It is rarely described in hyper IgD with periodic fever syndrome, cryopyrin associated periodic syndromes, TNF receptor-associated pe …
Autoinflammatory syndromes.
Galeazzi M, Gasbarrini G, Ghirardello A, Grandemange S, Hoffman HM, Manna R, Podswiadek M, Punzi L, Sebastiani GD, Touitou I, Doria A. Galeazzi M, et al. Clin Exp Rheumatol. 2006 Jan-Feb;24(1 Suppl 40):S79-85. Clin Exp Rheumatol. 2006. PMID: 16466630 Review.
The autoinflammatory diseases comprise both hereditary (Familial Mediterranean Fever, FMF; Mevalonate Kinase Deficiency, MKD; TNF Receptor Associated Periodic Syndrome, TRAPS; Cryopyrin Associated Periodic Syndrome, CAPS; Blau syndrome; Pyogenic steril …
The autoinflammatory diseases comprise both hereditary (Familial Mediterranean Fever, FMF; Mevalonate Kinase Deficiency, MKD; TNF Receptor A …
A Chinese girl of Blau syndrome with renal arteritis and a literature review.
Zeng Q, Liu H, Li G, Li Y, Guan W, Zhang T, Gong Y, Zhang X, Lv Q, Wu B, Xu H, Sun L. Zeng Q, et al. Pediatr Rheumatol Online J. 2023 Mar 13;21(1):23. doi: 10.1186/s12969-023-00804-z. Pediatr Rheumatol Online J. 2023. PMID: 36915122 Free PMC article. Review.
BACKGROUND: Blau syndrome is a rare autoinflammatory disease caused by autosomal dominant mutations in the CARD15/NOD2 gene. Vascular involvement is a rare phenotype in Blau syndrome patients. In this study, we aimed to describe a 20-year- old Chinese …
BACKGROUND: Blau syndrome is a rare autoinflammatory disease caused by autosomal dominant mutations in the CARD15/NOD2 gene. V …
87 results