These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

303 related articles for article (PubMed ID: 26509073)

  • 1. Autoinflammatory granulomatous diseases: from Blau syndrome and early-onset sarcoidosis to NOD2-mediated disease and Crohn's disease.
    Caso F; Galozzi P; Costa L; Sfriso P; Cantarini L; Punzi L
    RMD Open; 2015; 1(1):e000097. PubMed ID: 26509073
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis.
    Caso F; Costa L; Rigante D; Vitale A; Cimaz R; Lucherini OM; Sfriso P; Verrecchia E; Tognon S; Bascherini V; Galeazzi M; Punzi L; Cantarini L
    Autoimmun Rev; 2014 Dec; 13(12):1220-9. PubMed ID: 25182201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.
    Okafuji I; Nishikomori R; Kanazawa N; Kambe N; Fujisawa A; Yamazaki S; Saito M; Yoshioka T; Kawai T; Sakai H; Tanizaki H; Heike T; Miyachi Y; Nakahata T
    Arthritis Rheum; 2009 Jan; 60(1):242-50. PubMed ID: 19116920
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NOD2-associated diseases: Bridging innate immunity and autoinflammation.
    Borzutzky A; Fried A; Chou J; Bonilla FA; Kim S; Dedeoglu F
    Clin Immunol; 2010 Mar; 134(3):251-61. PubMed ID: 19467619
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Using genes to triangulate the pathophysiology of granulomatous autoinflammatory disease: NOD2, PLCG2 and LACC1.
    Szymanski AM; Ombrello MJ
    Int Immunol; 2018 Apr; 30(5):205-213. PubMed ID: 29538758
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations].
    Kanazawa N
    Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr; 30(2):123-32. PubMed ID: 17473515
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.
    Rosé CD; Doyle TM; McIlvain-Simpson G; Coffman JE; Rosenbaum JT; Davey MP; Martin TM
    J Rheumatol; 2005 Feb; 32(2):373-5. PubMed ID: 15693102
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NOD2/CARD15 disease associations other than Crohn's disease.
    Henckaerts L; Vermeire S
    Inflamm Bowel Dis; 2007 Feb; 13(2):235-41. PubMed ID: 17206682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review.
    Punzi L; Furlan A; Podswiadek M; Gava A; Valente M; De Marchi M; Peserico A
    Autoimmun Rev; 2009 Jan; 8(3):228-32. PubMed ID: 18718560
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis.
    Whyte MP; Lim E; McAlister WH; Gottesman GS; Trinh L; Veis DJ; Bijanki VN; Boden MG; Nenninger A; Mumm S; Buchbinder D
    J Bone Miner Res; 2018 Nov; 33(11):2071-2080. PubMed ID: 29933504
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nucleotide-binding oligomerization domain containing 2: structure, function, and diseases.
    Yao Q
    Semin Arthritis Rheum; 2013 Aug; 43(1):125-30. PubMed ID: 23352252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early-onset sarcoidosis caused by a rare CARD15/NOD2 de novo mutation and responsive to infliximab: a case report with long-term follow-up and review of the literature.
    La Torre F; Lapadula G; Cantarini L; Lucherini OM; Iannone F
    Clin Rheumatol; 2015 Feb; 34(2):391-5. PubMed ID: 24445386
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Blau syndrome-associated uveitis and the NOD2 gene.
    Pillai P; Sobrin L
    Semin Ophthalmol; 2013; 28(5-6):327-32. PubMed ID: 24010719
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of infantile Takayasu arteritis with a p.D382E NOD2 mutation: an unusual phenotype of Blau syndrome/early-onset sarcoidosis?
    Inoue Y; Kawaguchi Y; Shimojo N; Yamaguchi K; Morita Y; Nakano T; Arima T; Tomiita M; Kohno Y
    Mod Rheumatol; 2013 Jul; 23(4):837-9. PubMed ID: 22821420
    [TBL] [Abstract][Full Text] [Related]  

  • 15. How NOD2 mutations predispose to Crohn's disease?
    Vignal C; Singer E; Peyrin-Biroulet L; Desreumaux P; Chamaillard M
    Microbes Infect; 2007 Apr; 9(5):658-63. PubMed ID: 17379562
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nod2-Nodosome in a Cell-Free System: Implications in Pathogenesis and Drug Discovery for Blau Syndrome and Early-Onset Sarcoidosis.
    Iwasaki T; Kaneko N; Ito Y; Takeda H; Sawasaki T; Heike T; Migita K; Agematsu K; Kawakami A; Morikawa S; Mokuda S; Kurata M; Masumoto J
    ScientificWorldJournal; 2016; 2016():2597376. PubMed ID: 27403452
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The autoinflammatory diseases.
    Federici S; Caorsi R; Gattorno M
    Swiss Med Wkly; 2012; 142():w13602. PubMed ID: 22714396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new CARD15 mutation in Blau syndrome.
    van Duist MM; Albrecht M; Podswiadek M; Giachino D; Lengauer T; Punzi L; De Marchi M
    Eur J Hum Genet; 2005 Jun; 13(6):742-7. PubMed ID: 15812565
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.
    Aróstegui JI; Arnal C; Merino R; Modesto C; Antonia Carballo M; Moreno P; García-Consuegra J; Naranjo A; Ramos E; de Paz P; Rius J; Plaza S; Yagüe J
    Arthritis Rheum; 2007 Nov; 56(11):3805-13. PubMed ID: 17968944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W.
    van Steensel MA; Badeloe S; Winnepenninckx V; Vreeburg M; Steijlen PM; van Geel M
    Exp Dermatol; 2008 Dec; 17(12):1057-8. PubMed ID: 18616576
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.