AAAAAA

   
Results: 1-25 |
Results: 25

Authors: KOROLEVA IV SJOHOLM AG SCHALEN C
Citation: Iv. Koroleva et al., BINDING OF COMPLEMENT SUBCOMPONENT CLQ TO STREPTOCOCCUS-PYOGENES - EVIDENCE FOR INTERACTIONS WITH THE M5 AND FCRA76 PROTEINS, FEMS immunology and medical microbiology, 20(1), 1998, pp. 11-20

Authors: JUNKER A BAATRUP G SVEHAG SE WANG P HOLMSTROM E STURFELT G SJOHOLM AG
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

Authors: FREDRIKSON GN GULLSTRAND B WESTBERG J SJOHOLM AG UHLEN M TRUEDSSON L
Citation: Gn. Fredrikson et al., EXPRESSION OF PROPERDIN IN COMPLETE AND INCOMPLETE DEFICIENCY - NORMAL IN-VITRO SYNTHESIS BY MONOCYTES IN 2 CASES WITH PROPERDIN DEFICIENCYTYPE-II DUE TO DISTINCT MUTATIONS, Journal of clinical immunology, 18(4), 1998, pp. 272-282

Authors: FREDRIKSON GN GULLSTRAND B SCHNEIDER PM WITZELSCHLOMP K SJOHOLM AG ALPER CA AWDEH Z TRUEDSSON L
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

Authors: SKATTUM L MARTENSSON U SJOHOLM AG
Citation: L. Skattum et al., HYPOCOMPLEMENTEMIA CAUSED BY C3 NEPHRITIC FACTORS (C3 NEF) - CLINICALFINDINGS AND THE COINCIDENCE OF C3 NEF TYPE-II WITH ANTI-C1Q AUTOANTIBODIES, Journal of internal medicine, 242(6), 1997, pp. 455-464

Authors: SJOHOLM AG MARTENSSON U STURFELT G
Citation: Ag. Sjoholm et al., SERIAL ANALYSIS OF AUTOANTIBODY RESPONSES TO THE COLLAGEN-LIKE REGIONOF CLQ, COLLAGEN TYPE-II, AND DOUBLE-STRANDED DNA IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS, Journal of rheumatology, 24(5), 1997, pp. 871-878

Authors: TRUEDSSON L WESTBERG J FREDRIKSON GN SJOHOLM AG KUIJPER EJ FIJEN CAP SPATH PJ UHLEN M
Citation: L. Truedsson et al., HUMAN PROPERDIN DEFICIENCY HAS A HETEROGENEOUS GENETIC BACKGROUND, Immunopharmacology, 38(1-2), 1997, pp. 203-206

Authors: BERGE A KIHLBERG BM SJOHOLM AG BJORCK L
Citation: A. Berge et al., STREPTOCOCCAL PROTEIN-H FORMS SOLUBLE COMPLEMENT-ACTIVATING COMPLEXESWITH IGG, BUT INHIBITS COMPLEMENT ACTIVATION BY IGG-COATED TARGETS, The Journal of biological chemistry, 272(33), 1997, pp. 20774-20781

Authors: STURFELT G RYDGREN L TRUEDSSON L ALM P SJOHOLM AG
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

Authors: WOPENKA U THYSELL H SJOHOLM AG TRUEDSSON L
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

Authors: MARTENSSON U THIEL S JENSENIUS JC SJOHOLM AG
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

Authors: FREDRIKSON GN WESTBERG J KUIJPER EJ TIJSSEN CC SJOHOLM AG UHLEN M TRUEDSSON L
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

Authors: AKESSON P SJOHOLM AG BJORCK L
Citation: P. Akesson et al., PROTEIN SIC, A NOVEL EXTRACELLULAR PROTEIN OF STREPTOCOCCUS-PYOGENES INTERFERING WITH COMPLEMENT FUNCTION, The Journal of biological chemistry, 271(2), 1996, pp. 1081-1088

Authors: KIHLBERG BM SJOHOLM AG BJORCK L SJOBRING U
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

Authors: STURFELT G LENHOFF S SALLERFORS B NIVED O TRUEDSSON L SJOHOLM AG
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

Authors: WESTBERG J FREDRIKSON GN TRUEDSSON L SJOHOLM AG UHLEN M
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

Authors: JONSSON H STURFELT G MARTENSSON U TRUEDSSON L SJOHOLM AG
Citation: H. Jonsson et al., PROSPECTIVE ANALYSIS OF C1 DISSOCIATION AND COMPLEMENT ACTIVATION IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS, Clinical and experimental rheumatology, 13(5), 1995, pp. 573-580

Authors: AGARDI D PIGG M SJOHOLM AG TRUEDSSON L SPATH PJ KUIJPER EJ TIJSSEN CC TRANEBJAERG L GUSTAVSON KH ULFENDAHL PJ WADELIUS C
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

Authors: EKDAHL K TRUEDSSON L SJOHOLM AG BRACONIER JH
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

Authors: STURFELT G MARTENSSON U SJOHOLM AG
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

Authors: LITTORIN M TRUEDSSON L WELINDER H SKARPING G MARTENSSON U SJOHOLM AG
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

Authors: LINDGREN S HANSEN B SJOHOLM AG MANTHORPE R
Citation: S. Lindgren et al., COMPLEMENT ACTIVATION IN PATIENTS WITH PRIMARY SJOGRENS-SYNDROME - ANINDICATOR OF SYSTEMIC-DISEASE, Autoimmunity, 16(4), 1993, pp. 297-300

Authors: TRUEDSSON L ALPER CA AWDEH ZL JOHANSEN P SJOHOLM AG STURFELT G
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

Authors: FREDRIKSON GN TRUEDSSON L SJOHOLM AG
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

Authors: STURFELT G JONSSON H HELLMER G 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
Risultati: 1-25 |