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Similar articles for PubMed (Select 14516815)

1.

With a mere nod, uveitis enters a new era.

Rosenbaum JT, Planck SR, Davey MP, Iwanaga Y, Kurz DE, Martin TM.

Am J Ophthalmol. 2003 Oct;136(4):729-32. Review.

PMID:
14516815
2.

Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15).

Martin TM, Doyle TM, Smith JR, Dinulescu D, Rust K, Rosenbaum JT.

Am J Ophthalmol. 2003 Nov;136(5):933-5.

PMID:
14597055
3.

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 May-Jun;38(3):190-7. doi: 10.1080/03009740802464194.

PMID:
19169908
4.

CARD15 mutations in Blau syndrome.

Miceli-Richard C, Lesage S, Rybojad M, Prieur AM, Manouvrier-Hanu S, Häfner R, Chamaillard M, Zouali H, Thomas G, Hugot JP.

Nat Genet. 2001 Sep;29(1):19-20.

PMID:
11528384
5.

Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation.

Kurokawa T, Kikuchi T, Ohta K, Imai H, Yoshimura N.

Ophthalmology. 2003 Oct;110(10):2040-4. Review.

PMID:
14522785
6.

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. doi: 10.1002/art.24134.

7.

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.

8.

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.

9.

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.

PMID:
15693102
10.

Blau syndrome associated with a CARD15/NOD2 mutation.

Snyers B, Dahan K.

Am J Ophthalmol. 2006 Dec;142(6):1089-92. Epub 2006 Aug 2.

PMID:
17157607
11.

The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders.

Kambe N, Nishikomori R, Kanazawa N.

J Dermatol Sci. 2005 Aug;39(2):71-80. Review.

PMID:
15927452
12.

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. doi: 10.1016/j.autrev.2008.07.034. Epub 2008 Aug 19.

PMID:
18718560
13.

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 Jan-Feb;27(1):69-73. doi: 10.1111/j.1525-1470.2009.01060.x.

PMID:
20199415
14.

Blau syndrome revisited.

Rose CD, Martin TM, Wouters CH.

Curr Opin Rheumatol. 2011 Sep;23(5):411-8. doi: 10.1097/BOR.0b013e328349c430. Review.

PMID:
21788900
15.

Cloning, sequencing and expression analysis of the mouse NOD2/CARD15 gene.

Iwanaga Y, Davey MP, Martin TM, Planck SR, DePriest ML, Baugh MM, Suing CM, Rosenbaum JT.

Inflamm Res. 2003 Jun;52(6):272-6.

PMID:
12835899
16.

Nucleotide-binding oligomerization domain containing 2: structure, function, and diseases.

Yao Q.

Semin Arthritis Rheum. 2013 Aug;43(1):125-30. doi: 10.1016/j.semarthrit.2012.12.005. Epub 2013 Jan 24. Review.

PMID:
23352252
17.

[Blau syndrome--a chronic granulomatous, genetic disease].

Milman N, Byg KE.

Ugeskr Laeger. 2006 Oct 16;168(42):3612-4. Danish.

PMID:
17069723
18.

Blau syndrome.

Latkany P.

Ophthalmology. 2004 Apr;111(4):853; author reply 853-4. No abstract available.

PMID:
15051234
19.

Blau syndrome and related genetic disorders causing childhood arthritis.

Becker ML, Rose CD.

Curr Rheumatol Rep. 2005 Dec;7(6):427-33. Review.

PMID:
16303101
20.

Altered host:pathogen interactions conferred by the Blau syndrome mutation of NOD2.

Kim TH, Payne U, Zhang X, Iwanaga Y, Davey MP, Rosenbaum JT, Inman RD.

Rheumatol Int. 2007 Jan;27(3):257-62. Epub 2006 Nov 10.

PMID:
17096091
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