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The familial form of spondylarthropathy: a clinical study of 115 multiplex families. Groupe Français d'Etude Génétique des Spondylarthropathies.
Said-Nahal R, Miceli-Richard C, Berthelot JM, Duché A, Dernis-Labous E, Le Blévec G, Saraux A, Perdriger A, Guis S, Claudepierre P, Sibilia J, Amor B, Dougados M, Breban M. Said-Nahal R, et al. Arthritis Rheum. 2000 Jun;43(6):1356-65. doi: 10.1002/1529-0131(200006)43:6<1356::AID-ANR20>3.0.CO;2-Y. Arthritis Rheum. 2000. PMID: 10857795 Free article.
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. Miceli-Richard C, et al. Nat Genet. 2001 Sep;29(1):19-20. doi: 10.1038/ng720. Nat Genet. 2001. PMID: 11528384
CARD15/NOD2 analyses in spondylarthropathy.
Miceli-Richard C, Zouali H, Lesage S, Thomas G, Hugot JP, Said-Nahal R, Breban M. Miceli-Richard C, et al. Arthritis Rheum. 2002 May;46(5):1405-6. doi: 10.1002/art.10196. Arthritis Rheum. 2002. PMID: 12115249 Free article. No abstract available.
138 results