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Arthritis and Rheumatism|October 2, 2007
Laser Doppler flowmetry for assessing localized scleroderma in childrenLisa Weibel, Kevin J Howell, Maria Teresa Visentin, et al.
Plos One|October 25, 2012
Association of the IL-10 gene family locus on chromosome 1 with juvenile idiopathic arthritis (JIA)Ebun Omoyinmi, Paola Forabosco, Raja Hamaoui, et al.
Arthritis and Rheumatism|March 1, 2007
No evidence for genetic association of interferon regulatory factor 1 in juvenile idiopathic arthritisMark S Fife, Laura Gathercole, Emma M Ogilvie, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 24, 2007
Free Interleukin (IL)-18 levels, and the impact of IL18 and IL18BP genetic variation, in CHD patients and healthy menSimon R Thompson, Daniela Novick, Carmel J Stock, et al.
Arthritis Research & Therapy|September 9, 2006
Novel IL10 gene family associations with systemic juvenile idiopathic arthritisMark S Fife, Ana Gutierrez, Emma M Ogilvie, et al.
The British Journal of Ophthalmology|May 4, 2007
Ocular involvement in children with localised scleroderma: a multi-centre studyMaria Elisabetta Zannin, Giorgia Martini, Balu H Athreya, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|July 24, 2009
Validation of a protocol for the assessment of skin temperature and blood flow in childhood localised sclerodermaKevin J Howell, Antonia Lavorato, María Teresa Visentin, et al.
Arthritis Research & Therapy|March 4, 2005
Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control studyHulya Bukulmez, Mark Fife, Monica Tsoras, et al.
Arthritis Research & Therapy|February 21, 2013
Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literatureDorota M Rowczenio, Hadija Trojer, Tonia Russell, et al.
Archives of Dermatology|December 21, 2006
Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutationsKieron S Leslie, Helen J Lachmann, Elizabeth Bruning, et al.
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