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NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain.
Arthritis Rheum. 2009 Jun;60(6):1797-803. doi: 10.1002/art.24533.
Arthritis Rheum. 2009.
PMID: 19479837
Free PMC article.
Genotype analysis of polymorphisms in autoimmune susceptibility genes, CTLA-4 and PTPN22, in an acute anterior uveitis cohort.
Martin TM, Bye L, Modi N, Stanford MR, Vaughan R, Smith JR, Wade NK, Mackensen F, Suhler EB, Rosenbaum JT, Wallace GR.
Martin TM, et al.
Mol Vis. 2009;15:208-12. Epub 2009 Jan 26.
Mol Vis. 2009.
PMID: 19180256
Free PMC article.
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Incomplete penetrance of the NOD2 E383K substitution among members of a pediatric granulomatous arthritis pedigree.
Saulsbury FT, Wouters CH, Martin TM, Austin CR, Doyle TM, Goodwin KA, Rosé CD.
Saulsbury FT, et al.
Arthritis Rheum. 2009 Jun;60(6):1804-6. doi: 10.1002/art.24532.
Arthritis Rheum. 2009.
PMID: 19479836
Free article.
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The NOD2 defect in Blau syndrome does not result in excess interleukin-1 activity.
Martin TM, Zhang Z, Kurz P, Rosé CD, Chen H, Lu H, Planck SR, Davey MP, Rosenbaum JT.
Martin TM, et al.
Arthritis Rheum. 2009 Feb;60(2):611-8. doi: 10.1002/art.24222.
Arthritis Rheum. 2009.
PMID: 19180500
Free PMC article.
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