|1.||Martin, Tammy M: 13 articles (04/2012 - 10/2003)|
|2.||Rosenbaum, James T: 12 articles (06/2011 - 10/2003)|
|3.||Davey, Michael P: 10 articles (06/2011 - 10/2003)|
|4.||Punzi, Leonardo: 8 articles (01/2015 - 06/2005)|
|5.||Rose, Carlos D: 7 articles (06/2014 - 12/2005)|
|6.||Kanazawa, Nobuo: 7 articles (01/2014 - 02/2005)|
|7.||Planck, Stephen R: 7 articles (04/2010 - 10/2003)|
|8.||Rosenzweig, Holly L: 6 articles (05/2015 - 01/2008)|
|9.||Wouters, Carine H: 6 articles (06/2014 - 10/2006)|
|10.||Kambe, Naotomo: 6 articles (01/2014 - 02/2005)|
09/01/2010 - "Blau syndrome should be considered in the differential diagnosis of childhood uveitis and the genetic analysis of the CARD15/NOD2 gene is helpful in the diagnosis."
05/01/2015 - "To determine whether patients with juvenile systemic granulomatous disease (JSGD) (Blau syndrome) and uveitis have a characteristic ocular phenotype. "
01/01/2015 - "The etiology of Autoimmune chronic uveitis (ACU) is still unknown; NOD2/CARD15 gene mutations are responsible for the Blau Syndrome and can induce uveitis in animal models. "
09/01/2013 - "Blau syndrome-associated uveitis and the NOD2 gene."
06/01/2011 - "The innate immune receptor NOD2 is a genetic cause of uveitis (Blau syndrome). "
|2.||Sarcoidosis (Schaumann Disease)
04/01/2013 - "[The present and the prospect of study on Blau syndrome/early-onset sarcoidosis]."
12/01/2007 - "The aim of this study was to evaluate whether ethnic Danes with sarcoidosis have CARD15 mutations associated with Blau syndrome. "
11/01/2015 - "Role of NOD2 Pathway Genes in Sarcoidosis Cases with Clinical Characteristics of Blau Syndrome."
12/01/2014 - "Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis."
06/01/2011 - "The genetic and immunophenotypic characteristics of a 3-year-old patient with Blau syndrome (BS), an early onset sarcoidosis caused by mutations in NOD2, were investigated. "
|3.||Crohn Disease (Crohn's Disease)
10/31/2007 - "Recent studies have implicated Single Nucleotide Polymorphisms (SNPs) of the NOD2/CARD15 gene with the onset of several Inflammatory Bowel Disorders (Crohn's Disease, Blau syndrome) and the progression of several malignant diseases. "
12/01/2003 - "Together, studies on Nod2 (Card15) provide a conceptual link between inflammatory disorders, such as Crohn's disease and Blau syndrome, and bacterial sensing."
12/01/2014 - "Polymorphisms in NOD2 are the cause of the inflammatory disorder Blau syndrome and act as susceptibility factors for the inflammatory bowel condition Crohn's disease. "
08/01/2013 - "There are more than 100 NOD2 gene mutations, some of which have been linked to diseases such as Crohn disease, Blau syndrome, and NOD2-associated autoinflammatory disease (NAID). "
01/15/2013 - "Dysregulation of NOD2 signaling is associated with inflammatory diseases, such as Crohn's disease and Blau syndrome. "
01/01/2014 - "However, detailed information on arthritis in Blau syndrome on which the therapeutic strategy should be based on is lacking. "
01/01/2014 - "Arthritis is the most frequent manifestation of Blau syndrome, an autoinflammatory disorder caused by the genetic mutation of NOD2. "
12/01/2005 - "Blau syndrome and related genetic disorders causing childhood arthritis."
02/01/2005 - "These data suggest that sporadic granulomatous arthritis may in fact be the sporadic form of Blau syndrome, but arising from a spontaneous neomutation. "
02/01/2005 - "We investigated the hypothesis that an individual with sporadic early onset granulomatous arthritis may have a Blau syndrome mutation in CARD15/NOD2. "
|5.||Cryopyrin-Associated Periodic Syndromes
02/01/2007 - "NALP3 and NOD2, which belong to a cytosolic subgroup of PRMs, dubbed Nod-like-receptors (NLRs), have been associated recently with inflammatory diseases, specifically Crohn's disease and Blau syndrome (NOD2) and familial cold autoinflammatory syndrome, Muckle-Wells syndrome and chronic infantile neurological cutaneous and articular syndrome (NALP3). "
02/01/2009 - "Taken together, these data suggest that in contrast to related IL-1beta-dependent autoinflammatory cryopyrinopathies, Blau syndrome is not mediated by excess IL-1beta or other IL-1 activity."
04/01/2007 - "Recent studies have described the genetic association of polymorphisms in NOD-like receptor genes with complex chronic inflammatory barrier diseases, such as Crohn's disease and asthma and with rare auto-inflammatory syndromes including familial cold urticaria, Muckle-Wells syndrome and Blau syndrome. "
12/01/2012 - "The term autoinflammatory syndromes includes a broad variety of disorders, including cryopyrin-associated periodic syndromes (CAPS) such as neonatal onset multisystem inflammatory disease (NOMID), familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), periodic fever syndromes, including familial Mediterranean fever (FMF), TNF receptor-1 associated periodic syndrome (TRAPS), and Blau syndrome. "
01/01/2007 - "Furthermore, mutations in the genes that encode these proteins have been associated with complex inflammatory disorders including Crohn's disease, asthma, familial cold urticaria, Muckle-Wells syndrome, and Blau syndrome. "
|2.||glucuronyl glucosamine glycan sulfate (Vessel)
|4.||autosomal dominant familial Periodic fever
|5.||Interleukin-1 (Interleukin 1)
|6.||Immunoglobulin D (IgD)
|7.||Pyogenic arthritis, pyoderma gangrenosum, and acne
|8.||Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)
|9.||Proteins (Proteins, Gene)