BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 28639104)

  • 21. Blau syndrome associated with a CARD15/NOD2 mutation.
    Snyers B; Dahan K
    Am J Ophthalmol; 2006 Dec; 142(6):1089-92. PubMed ID: 17157607
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Early-onset sarcoidosis/Blau syndrome].
    Kambe N; Satoh T; Nakano M; Nakamura Y; Matsue H
    Nihon Rinsho Meneki Gakkai Kaishi; 2011; 34(5):378-81. PubMed ID: 22041425
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity.
    Rose CD
    Pediatr Dermatol; 2017 Mar; 34(2):216-218. PubMed ID: 27874205
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Favourable effect of TNF-alpha inhibitor (infliximab) on Blau syndrome in monozygotic twins with a de novo CARD15 mutation.
    Milman N; Andersen CB; Hansen A; van Overeem Hansen T; Nielsen FC; Fledelius H; Ahrens P; Nielsen OH
    APMIS; 2006 Dec; 114(12):912-9. PubMed ID: 17207093
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Sporadic Blau syndrome with onset of widespread granulomatous dermatitis in the newborn period.
    Stoevesandt J; Morbach H; Martin TM; Zierhut M; Girschick H; Hamm H
    Pediatr Dermatol; 2010; 27(1):69-73. PubMed ID: 20199415
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Intractable leg ulcers in Blau syndrome.
    Kamio Y; Kanazawa N; Mine Y; Utani A
    J Dermatol; 2016 Sep; 43(9):1096-7. PubMed ID: 26969879
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Optic nerve and retinal features in uveitis associated with juvenile systemic granulomatous disease (Blau syndrome).
    Carreño E; Guly CM; Chilov M; Hinchcliffe A; Arostegui JI; Lee RW; Dick AD; Ramanan AV
    Acta Ophthalmol; 2015 May; 93(3):253-7. PubMed ID: 25209167
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Role of NOD2 Pathway Genes in Sarcoidosis Cases with Clinical Characteristics of Blau Syndrome.
    Bello GA; Adrianto I; Dumancas GG; Levin AM; Iannuzzi MC; Rybicki BA; Montgomery C
    Am J Respir Crit Care Med; 2015 Nov; 192(9):1133-5. PubMed ID: 26517420
    [No Abstract]   [Full Text] [Related]  

  • 34. Clinical Profile in Genetically Proven Blau Syndrome: A Case Series from South India.
    Babu K; Rao AP
    Ocul Immunol Inflamm; 2021 Feb; 29(2):250-256. PubMed ID: 32293936
    [No Abstract]   [Full Text] [Related]  

  • 35. A Case of Blau Syndrome with NOD2 E383K Mutation.
    Harada J; Nakajima T; Kanazawa N
    Pediatr Dermatol; 2016 Nov; 33(6):e385-e387. PubMed ID: 27339507
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Blau syndrome revisited.
    Rose CD; Martin TM; Wouters CH
    Curr Opin Rheumatol; 2011 Sep; 23(5):411-8. PubMed ID: 21788900
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members.
    Milman N; Ursin K; Rødevand E; Nielsen FC; Hansen TV
    Scand J Rheumatol; 2009; 38(3):190-7. PubMed ID: 19169908
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Blau syndrome, the prototypic auto-inflammatory granulomatous disease.
    Wouters CH; Maes A; Foley KP; Bertin J; Rose CD
    Pediatr Rheumatol Online J; 2014; 12():33. PubMed ID: 25136265
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A sporadic case of granulomatous disease negative for NOD2 mutations and mimicking Blau syndrome.
    Oda F; Murakami M; Hanakawa Y; Tohyama M; Nakano N; Nishikomori R; Kambe N; Sayama K
    Clin Exp Dermatol; 2018 Jan; 43(1):57-58. PubMed ID: 29082556
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.