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Journal Abstract Search

312 related items for PubMed ID: 22821420

  • 1. 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
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  • 2. [Early-onset sarcoidosis/Blau syndrome].
    Kambe N, Satoh T, Nakano M, Nakamura Y, Matsue H.
    Nihon Rinsho Meneki Gakkai Kaishi; 2011 Jul; 34(5):378-81. PubMed ID: 22041425
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  • 3. Blau arteritis resembling Takayasu disease with a novel NOD2 mutation.
    Khubchandani RP, Hasija R, Touitou I, Khemani C, Wouters CH, Rose CD.
    J Rheumatol; 2012 Sep; 39(9):1888-92. PubMed ID: 22859352
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  • 5. 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
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  • 6. A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
    Ong LT, Nachbur U, Rowczenio D, Ziegler JB, Fischer E, Lin MW.
    Innate Immun; 2017 Oct; 23(7):578-583. PubMed ID: 28836875
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  • 9. Uveitis in Blau syndrome from a de novo mutation of the NOD2/CARD15 gene.
    Raiji VR, Miller MM, Jung LK.
    J AAPOS; 2011 Apr; 15(2):205-7. PubMed ID: 21596301
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  • 10. Granulomatous pneumonitis associated with adult-onset Blau-like syndrome.
    Yao Q, Piliang M, Nicolacakis K, Arrossi A.
    Am J Respir Crit Care Med; 2012 Sep 01; 186(5):465-6. PubMed ID: 22942351
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  • 11. Exacerbation of symptoms in Blau syndrome/early-onset sarcoidosis following delivery.
    Mizawa M, Makino T, Nakamura T, Yamaguchi S, Taki H, Shimizu T.
    Eur J Dermatol; 2015 Sep 01; 25(6):620-2. PubMed ID: 26712281
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  • 13. Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis.
    Takada S, Saito MK, Kambe N.
    G Ital Dermatol Venereol; 2020 Oct 01; 155(5):537-541. PubMed ID: 32618442
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  • 17. Blau syndrome-associated uveitis and the NOD2 gene.
    Pillai P, Sobrin L.
    Semin Ophthalmol; 2013 Oct 01; 28(5-6):327-32. PubMed ID: 24010719
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  • 18. Blau syndrome with a rare mutation in exon 9 of NOD2 gene.
    Velickovic J, Silan F, Bir FD, Silan C, Albuz B, Ozdemir O.
    Autoimmunity; 2019 Oct 01; 52(7-8):256-263. PubMed ID: 31556326
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  • 19. Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism.
    Mensa-Vilaro A, Cham WT, Tang SP, Lim SC, González-Roca E, Ruiz-Ortiz E, Ariffin R, Yagüe J, Aróstegui JI.
    Arthritis Rheumatol; 2016 Apr 01; 68(4):1039-44. PubMed ID: 26606664
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  • 20. Blau Syndrome With Delayed Cutaneous Manifestations: A Case Report.
    Panah E, Garfield E, Zahirsha Z, Muhlbauer A, Lake E, Speiser J.
    Am J Dermatopathol; 2024 Jun 01; 46(6):381-382. PubMed ID: 38648024
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