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]