BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 37246600)

  • 1. Blau syndrome with NOD2 mutation in a 54-year-old man: A case report.
    Wang Z; Yang M; Zhang Q; Zhang S; Sui H; Liu J; Yang Q
    Int J Rheum Dis; 2023 Oct; 26(10):2080-2084. PubMed ID: 37246600
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Blau syndrome with pulmonary nodule in a child.
    Su J; Liu D
    Australas J Dermatol; 2021 May; 62(2):217-220. PubMed ID: 33742458
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes.
    Okazaki F; Wakiguchi H; Korenaga Y; Nakamura T; Yasudo H; Uchi S; Yanai R; Asano N; Hoshii Y; Tanabe T; Izawa K; Honda Y; Nishikomori R; Uchida K; Eishi Y; Ohga S; Hasegawa S
    Pediatr Rheumatol Online J; 2021 Feb; 19(1):18. PubMed ID: 33602264
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel Pathogenic
    Rodrigues FG; Petrushkin H; Webster AR; Bickerstaff M; Moraitis E; Rowczenio D; Aróstegui JI; Westcott M
    Ophthalmic Genet; 2021 Dec; 42(6):753-764. PubMed ID: 34251956
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Lipogranulomatous subconjunctival nodules: a novel presentation in Blau syndrome.
    Ahmad M; Hermanson ME; Enzenauer R; Palestine A; Lin C; Meeks N; McCourt E
    J AAPOS; 2017 Jun; 21(3):249-251. PubMed ID: 28532706
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the
    Matsuda T; Kambe N; Ueki Y; Kanazawa N; Izawa K; Honda Y; Kawakami A; Takei S; Tonomura K; Inoue M; Kobayashi H; Okafuji I; Sakurai Y; Kato N; Maruyama Y; Inoue Y; Otsubo Y; Makino T; Okada S; Kobayashi I; Yashiro M; Ito S; Fujii H; Kondo Y; Okamoto N; Ito S; Iwata N; Kaneko U; Doi M; Hosokawa J; Ohara O; Saito MK; Nishikomori R; ;
    Ann Rheum Dis; 2020 Nov; 79(11):1492-1499. PubMed ID: 32647028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Granulomatous skin involvement in a patient with an unusual NOD2 mutation.
    Kuye IO; Adisa M; Nazarian RM; Arvikar SL; Smith GP
    Australas J Dermatol; 2017 May; 58(2):142-144. PubMed ID: 26768519
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis.
    Takada S; Saito MK; Kambe N
    G Ital Dermatol Venereol; 2020 Oct; 155(5):537-541. PubMed ID: 32618442
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial Blau syndrome:First molecularly confirmed report from India.
    Janarthanan M; Poddar C; Sudharshan S; Seabra L; Crow YJ
    Indian J Ophthalmol; 2019 Jan; 67(1):165-167. PubMed ID: 30574935
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 25(6):620-2. PubMed ID: 26712281
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis.
    Zhong Z; Ding J; Su G; Liao W; Gao Y; Zhu Y; Deng Y; Li F; Du L; Gao Y; Yang P
    Ophthalmology; 2022 Jul; 129(7):821-828. PubMed ID: 35314268
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Blau Syndrome: Report of a Rare Entity with Congenital Ostium Secundum Atrial Septal Defect in a 7-year-old Chinese Girl.
    Yang XH; Lin L; Sun JF; Jiang YQ
    Acta Derm Venereol; 2019 Sep; 99(10):923-924. PubMed ID: 31120540
    [No Abstract]   [Full Text] [Related]  

  • 15. A Novel Mutation in Helical Domain 2 of NOD2 in Sporadic Blau Syndrome.
    Jain L; Gupta N; Reddy MM; Mittal R; Barik MR; Panigrahi B; Monie T; Basu S
    Ocul Immunol Inflamm; 2018; 26(2):292-294. PubMed ID: 27625029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blau syndrome: a case report from Palestine.
    Iriqat S; Safieh MA; Fatouleh M; Alkaiyat A
    Pediatr Rheumatol Online J; 2021 Aug; 19(1):138. PubMed ID: 34465352
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 46(6):381-382. PubMed ID: 38648024
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Blau syndrome with a rare mutation in exon 9 of
    Velickovic J; Silan F; Bir FD; Silan C; Albuz B; Ozdemir O
    Autoimmunity; 2019; 52(7-8):256-263. PubMed ID: 31556326
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a novel missense mutation in the NOD2 gene in a Chinese child with early-onset sarcoidosis.
    Wang X; Zhang X; Zhang W; Sun J
    Indian J Dermatol Venereol Leprol; 2018; 84(5):645. PubMed ID: 29067935
    [No Abstract]   [Full Text] [Related]  

  • 20. A Novel NOD2-associated Mutation and Variant Blau Syndrome: Phenotype and Molecular Analysis.
    Ebrahimiadib N; Samra KA; Domina AM; Stiles ER; Ewer R; Bocian CP; Foster CS
    Ocul Immunol Inflamm; 2018; 26(1):57-64. PubMed ID: 27419275
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.