IVIG blocks complement deposition mediated by anti-GM1 antibodies in multifocal motor neuropathy von Yuki, N, Watanabe, H, Nakajima, T, Späth, P J

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IVIG – mechanisms of action von Simon, H. U., Späth, P. J.

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Glomerulonephritis in a patient with complement factor I deficiency von Sadallah, Salima, Gudat, Fred, Laissue, Jean A., Spath, Peter J., Schifferli, Jürg-Alfred

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Hypocomplementemic urticarial vasculitis or systemic lupus erythematosus? von Trendelenburg, Marten, Courvoisier, Salome, Späth, Peter J., Moll, Solange, Mihatsch, Michael, Itin, Peter, Schifferli, Jürg A.

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Hereditary complement factor I deficiency von VYSE, T.J., SPÄTH, P.J., DAVIES, K.A., MORLEY, B.J., PHILIPPE, P., ATHANASSIOU, P., GILES, C.M., WALPORT, M.J.

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A C3 convertase assay for nephritic factor functional activity von Jelezarova, Emiliana, Schlumberger, Markus, Sadallah, Salima, Späth, Peter J., Schifferli, Jürg A., Lutz, Hans U.

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Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G... von SPÄTH, P. J, SJÖHOLM, A. G, WADELIUS, C, TRUEDSSON, L, FREDRIKSON, G. N, MISIANO, G, SCHERZ, R, SCHAAD, U. B, UHRING-LAMBERT, B, HAUPTMANN, G, WESTBERG, J, UHLEN, M

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Immunoglobulin G for the Treatment of Chronic Pain: Report of an Expert Workshop von Tamburin, Stefano, Borg, Kristian, Caro, Xavier J., Jann, Stefano, Clark, Alexander J., Magrinelli, Francesca, Sobue, Gen, Werhagen, Lars, Zanette, Giampietro, Koike, Haruki, Späth, Peter J., Vincent, Angela, Goebel, Andreas

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Intravenously applied IgG stimulates complement attenuation in a complement-dependent autoimmune disease at the amplifying C3 convertase level von Lutz, Hans U., Stammler, Pia, Bianchi, Valentina, Trüeb, Ralph M., Hunziker, Thomas, Burger, Reinhard, Jelezarova, Emiliana, Späth, Peter J.

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Human properdin deficiency has a heterogeneous genetic background von Truedsson, L., Westberg, J., Nordin Fredrikson, G., Sjöholm, A.G., Kuijper, E.J., Fijen, C.A.P., Späth, P.J., Uhlén, M.

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Screening for complement deficiency in bacterial meningitis von Ernst, T, Späth, PJ, Aebi, C, Schaad, UB, Bianchetti, MG

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Complement profiles in human skin lymph during the course of irritant contact dermatitis von Brand, C U, Späth, P J, Hunziker, T, Limat, A, Braathen, L R

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The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure von Witzel-Schlomp, K, Spath, PJ, Hobart, MJ, Fernie, BA, Rittner, C, Kaufmann, T, Schneider, PM

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Effect of Fibronectin on C3b and Fc Receptor-mediated Phagocytosis by Peripheral Blood Monocytes in Uraemic Patients von Pertosa, G., Mastrolitti, R.T., Späth, P.J., Fracasso, A.R., Manno, C., Schena, F.P.

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Malignancy masquerading as food hypersensitivity von Scheidegger, E. P., Späth, P. J., Furrer, M., Vogt, M., Fontana, A., Wüthrich, B.

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High doses of immunoglobulin G attenuate immune aggregate-mediated complement activation by enhancing physiologic cleavage of C3b in C3bn-IgG complexes von LUTZ, H. U, STAMMLER, P, JELEZAROVA, E, NATER, M, SPÄTH, P. J

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Genetic detection of the silent allele (Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components von Alvarez, Victoria, Coto, Eliecer, Setién, Fernando, Spath, Peter J., López-Larrea, Carlos

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Laboratory workshop on the characterization of anti-platelet antibodies in immune thrombocytopenic purpura von Gerber, Hans, Sp th, Peter J., Perret, Beat A., Burckhardt, Johann J.

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Human serum induced opsonization of immunoglobulin G-coated polystyrene microspheres with complement components C3 and C4 as measured by flow cytometry von Spycher, M.O., Spycher-Burger, M., Späth, P.J., Burckhardt, J.J.

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Solubilization of immune precipitates by complement in the absence of properdin or factor D von Späth, P.J., Pascual, M., Meyer-Hänni, Liselotte, Schaad, U.B., Schifferli, J.A.

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