Variant form of STAT4 is associated with primary Sjögren's syndrome von Korman, B D, Alba, M I, Le, J M, Alevizos, I, Smith, J A, Nikolov, N P, Kastner, D L, Remmers, E F, Illei, G G

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Evaluation of KIR3DL1/KIR3DS1 polymorphism in Behçet’s disease von Erer, B, Takeuchi, M, Ustek, D, Tugal-Tutkun, I, Seyahi, E, Özyazgan, Y, Duymaz-Tozkir, J, Gül, A, Kastner, D L, Remmers, E F, Ombrello, M J

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OP0174 Exome sequencing identifies a hypermorphic missense mutation in the PLCG2 gene as the cause of a dominantly inherited autoinflammatory disease with immunodeficiency von Aksentijevich, I., Zhou, Q., Lee, G.-S., Katan, M., Datta, S., Milner, J., Khan, J., Kastner, D.L.

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Mice with mutations of TNFRSF1A may reveal insights into pathogenesis of TRAPS, a dominantly inherited autoinflammatory disease von Komarow, H.D., Chae, J.J., Raben, N., Wood, G., Kastner, D.L.

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A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts von Shinar, Y, Ben-Zeev, B, Brand, N, Lahat, H, Gross-Zur, V, MacGregor, D, Bahan, T, Kastner, D L, Pras, E

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Lack of Evidence for an Association between Two Genetic Polymorphisms in the Tumor Necrosis Factor Receptor 1 Gene and Multiple Sclerosis in Ashkenazi Jews von Pras, E., Aksentijevich, I., Shinar, Y., Kastner, D.L., Achiron, A.

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Refined mapping of the gene causing familial mediterranean fever, by linkage and homozygosity studies von AKSENTIJEVICH, I, PRAS, E, DEAN, M, PRAS, M, AMOS, C. I, KASTNER, D. L, GRUBERG, L, YANG SHEN, HOLMAN, K, HELLING, S, PROSEN, L, SUTHERLAND, G. R, RICHARDS, R. I, RAMSBURG, M

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Familial Mediterranean Fever (FMF) in Moroccan Jews: Demonstration of a founder effect by extened haplotype analysis von Aksentijevich, I., Pras, E., Helling, S., Prosen, L., Kastner, D.L., Gruberg, L., Pras, M.

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Portable radiation spectrometer using low power digital pulse processing von Jordanov, V.T., Hall, D.L., Kastner, M., Woodward, G.H., Zakrzewski, R.A.

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