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Citation: A. Junker et al., BINDING OF PROPERDIN TO SOLID-PHASE IMMUNE-COMPLEXES - CRITICAL ROLE OF THE CLASSICAL ACTIVATION PATHWAY OF COMPLEMENT, Scandinavian journal of immunology, 47(5), 1998, pp. 481-486
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Citation: Gn. Fredrikson et al., CHARACTERIZATION OF NONEXPRESSED C4 GENES IN A CASE OF COMPLETE C4 DEFICIENCY - IDENTIFICATION OF A NOVEL POINT MUTATION LEADING TO A PREMATURE STOP CODON, Human immunology, 59(11), 1998, pp. 713-719
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Citation: G. Sturfelt et al., C1 INHIBITOR DEFICIENCY IN A PATIENT WITH RHEUMATOID-ARTHRITIS - INCREASED RISK OF ADVERSE-EFFECTS OF PENICILLAMINE, Journal of rheumatology, 23(2), 1996, pp. 378-381
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Citation: U. Wopenka et al., C4 PHENOTYPES IN IGA NEPHROPATHY - DISEASE PROGRESSION ASSOCIATED WITH C4A DEFICIENCY BUT NOT WITH C4 ISOTYPE CONCENTRATIONS, Clinical nephrology, 45(3), 1996, pp. 141-145
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Citation: U. Martensson et al., HUMAN AUTOANTIBODIES AGAINST C1Q - LACK OF CROSS-REACTIVITY WITH THE COLLECTINS MANNAN-BINDING PROTEIN, LUNG SURFACTANT PROTEIN-A AND BOVINE CONGLUTININ, Scandinavian journal of immunology, 43(3), 1996, pp. 314-320
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Citation: Gn. Fredrikson et al., MOLECULAR CHARACTERIZATION OF PROPERDIN DEFICIENCY TYPE-III - DYSFUNCTION PRODUCED BY A SINGLE-POINT MUTATION IN EXON-9 OF THE STRUCTURAL GENE CAUSING A TYROSINE TO ASPARTIC-ACID INTERCHANGE, The Journal of immunology, 157(8), 1996, pp. 3666-3671
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SJOHOLM AG
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Citation: Bm. Kihlberg et al., CHARACTERIZATION OF THE BINDING-PROPERTIES OF PROTEIN LG, AN IMMUNOGLOBULIN-BINDING HYBRID PROTEIN, European journal of biochemistry, 240(3), 1996, pp. 556-563
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Citation: G. Sturfelt et al., TRANSPLANTATION WITH ALLOGENIC BONE-MARROW FROM A DONOR WITH SYSTEMICLUPUS-ERYTHEMATOSUS (SLE) - SUCCESSFUL OUTCOME IN THE RECIPIENT AND INDUCTION OF AN SLE FLARE IN THE DONOR, Annals of the Rheumatic Diseases, 55(9), 1996, pp. 638-641
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Citation: J. Westberg et al., SEQUENCE-BASED ANALYSIS OF PROPERDIN DEFICIENCY - IDENTIFICATION OF POINT MUTATIONS IN 2 PHENOTYPIC FORMS OF AN X-LINKED IMMUNODEFICIENCY, Genomics, 29(1), 1995, pp. 1-8
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Citation: D. Agardi et al., FLUORESCENT DETECTION OF MICROSATELLITE POLYMORPHISMS - PROPERDIN DEFICIENCY LINKED TO PFC MICROSATELLITE, Experimental and clinical immunogenetics, 12(2), 1995, pp. 111-114
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Citation: K. Ekdahl et al., COMPLEMENT ANALYSIS IN ADULT PATIENTS WITH A HISTORY OF BACTEREMIC PNEUMOCOCCAL INFECTIONS OR RECURRENT PNEUMONIA, Scandinavian journal of infectious diseases, 27(2), 1995, pp. 111-117
Citation: G. Sturfelt et al., ANTIBODIES TO C1Q AND COLLAGEN TYPE-II IN PATIENTS WITH SLE - SERIAL INVESTIGATION AND LACK OF MAJOR CROSS-REACTION, Arthritis and rheumatism, 38(9), 1995, pp. 118-118
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Citation: M. Littorin et al., ACUTE RESPIRATORY DISORDER, RHINOCONJUNCTIVITIS AND FEVER ASSOCIATED WITH THE PYROLYSIS OF POLYURETHANE DERIVED FROM DIPHENYLMETHANE DIISOCYANATE, Scandinavian journal of work, environment & health, 20(3), 1994, pp. 216-222
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Citation: L. Truedsson et al., CHARACTERIZATION OF TYPE-I COMPLEMENT C2-DEFICIENCY MHC HAPLOTYPES - STRONG CONSERVATION OF THE COMPLOTYPE HLA-B-REGION AND ABSENCE OF DISEASE ASSOCIATION DUE TO LINKED CLASS-II GENES/, The Journal of immunology, 151(10), 1993, pp. 5856-5863
Citation: Gn. Fredrikson et al., NEW PROCEDURE FOR THE DETECTION OF COMPLEMENT DEFICIENCY BY ELISA - ANALYSIS OF ACTIVATION PATHWAYS AND CIRCUMVENTION OF RHEUMATOID-FACTOR INFLUENCE, Journal of immunological methods, 166(2), 1993, pp. 263-270
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SJOHOLM AG
Citation: G. Sturfelt et al., CLUSTERING OF NEUTROPHIL LEUKOCYTES IN SERUM - POSSIBLE ROLE OF C1Q-CONTAINING IMMUNE-COMPLEXES, Clinical and experimental immunology, 93(2), 1993, pp. 237-241