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

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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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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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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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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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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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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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Humoral immune response to pneumococcal antigen 23-F in an asplenic patient with recurrent fulminant pneumococcaemia von Zimmerli, W., Schaffner, A., Scheidegger, C., Scherz, R., Späth, P.J.

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Complement in chronic cutaneous lupus erythematosus von Hunziker, Th, Mollnes, T.E., Misiano, G., Späth, P.J.

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Immunoglobulin-mediated shifting of immune complexes to increased complement-dependent solubility and immunoadherence von Spycher, M.O., Späth, P.J., Hässig, A., Nydegger, U.E.

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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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High doses of antigen-nonspecific IgG do not inhibit pemphigus acantholysis in skin organ cultures von HUNZIKER, T, NYDEGGER, U. E, SPATH, P. J, GERBER, H. A, HESS, M, WIESMANN, U, KREBS, A

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Chronic immune thrombocytopenic purpura ? Immunological analyses of a patient pre- and post-HIV seroconversion von Sp th, P. J., Elisa, A., B hlmann, U., Luginb hl, L., Imbach, P.

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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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