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- 2018
-
Mark
Age and sex-associated changes of complement activity and complement levels in a healthy caucasian population
(
- Contribution to journal › Article
- 2015
-
Mark
Reversal of Immunoglobulin. A Deficiency in Children
(
- Contribution to journal › Article
-
Mark
Heat differentiated complement factor profiling.
(
- Contribution to journal › Article
-
Mark
Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency.
(
- Contribution to journal › Article
-
Mark
European Union funded project on the development of a whole complement deficiency screening ELISA-A story of success and an exceptional manager: Mohamed R. Daha.
(
- Contribution to journal › Scientific review
-
Mark
Anti-C1q antibodies in systemic lupus erythematosus.
(
- Contribution to journal › Article
-
Mark
Classical pathway deficiencies - A short analytical review.
(
- Contribution to journal › Scientific review
-
Mark
Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated Donor.
(
- Contribution to journal › Article
- 2014
-
Mark
Platelet activation and anti-phospholipid antibodies collaborate in the activation of the complement system on platelets in systemic lupus erythematosus.
(
- Contribution to journal › Article
-
Mark
Serological assessment for celiac disease in IgA deficient adults.
(
- Contribution to journal › Article
-
Mark
Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings.
(
- Contribution to journal › Article
- 2013
-
Mark
Contribution of IKBKE and IFIH1 gene variants to SLE susceptibility
(
- Contribution to journal › Article
- 2012
-
Mark
Vaccination against encapsulated bacteria in hereditary C2 deficiency results in antibody response and opsonization due to antibody-dependent complement activation.
(
- Contribution to journal › Article
-
Mark
Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene
(
- Contribution to journal › Article
-
Mark
Neutrophil Extracellular Traps That Are Not Degraded in Systemic Lupus Erythematosus Activate Complement Exacerbating the Disease.
(
- Contribution to journal › Article
- 2011
-
Mark
Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency.
(
- Contribution to journal › Article
-
Mark
Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations
(
- Contribution to journal › Article
-
Mark
Complement deficiency states and associated infections.
(
- Contribution to journal › Article
- 2010
-
Mark
Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases
(
- Contribution to journal › Article
-
Mark
Sensitive and specific assays for C3 nephritic factors permit dissection of mechanisms underlying complement dysregulation
(
- Contribution to journal › Published meeting abstract
-
Mark
Homozygosity For a Novel Mutation in the C1q C Chain Gene in a Turkish Family With Hereditary C1q Deficiency
(
- Contribution to journal › Article
- 2009
-
Mark
Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjogren's syndrome
(
- Contribution to journal › Article
-
Mark
C1q inhibits immune complex induced IFN-alpha production in plasmacytoid dendritic cells-A novel link between C1q deficiency and SLE pathogenesis
2009) 12th European Meeting on Complement in Human Disease In Molecular Immunology 46(14). p.2857-2857(
- Contribution to journal › Published meeting abstract
-
Mark
Influence of IgG allotypes on defense against Haemophilus influenzae type b in children-A complement-dependent mechanism?
2009) 12th European Meeting on Complement in Human Disease In Molecular Immunology 46(14). p.2867-2868(
- Contribution to journal › Published meeting abstract
-
Mark
Neutrophil degranulation and complement release in ANCA-associated vasculitis: an in vitro study
(
- Contribution to journal › Published meeting abstract
-
Mark
Complement classical pathway components are all important in clearance of apoptotic and secondary necrotic cells.
(
- Contribution to journal › Article
-
Mark
Mannose-binding lectin as a risk factor for acute coronary syndromes.
(
- Contribution to journal › Article
-
Mark
Genetic, molecular and functional analyses of complement factor I deficiency.
(
- Contribution to journal › Article
- 2008
-
Mark
SLE serum induces classical caspase-dependent apoptosis independent of death receptors
(
- Contribution to journal › Article
-
Mark
Impaired opsonization with C3b and phagocytosis of Streptococcus pneumoniae in sera from subjects with defects in the classical complement pathway
(
- Contribution to journal › Article
-
Mark
Functional C1-inhibitor diagnostics in hereditary angioedema: Assay evaluation and recommendations
(
- Contribution to journal › Article
-
Mark
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes.
(
- Contribution to journal › Article
- 2007
-
Mark
Design of recombinant antibody microarrays for serum protein profiling: Targeting of complement proteins
(
- Contribution to journal › Article
-
Mark
Gene-environment interactions in the aetiology of systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Complement analysis in the 21st century
(
- Contribution to journal › Article
-
Mark
Allergiska och immunologiska tillstånd.
2007) p.1087-1099(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
A polymorphic variant in the MHC2TA gene is not associated with systemic lupus erythematosus
(
- Contribution to journal › Article
- 2006
-
Mark
Mannan-binding lectin activates C3 and the alternative complement pathway without involvement of C2.
(
- Contribution to journal › Article
-
Mark
Complement deficiency and disease: An update.
(
- Contribution to journal › Scientific review
-
Mark
Homozygosity for the IgG2 subclass allotype G2M(n) protects against severe infection in hereditary C2 deficiency
(
- Contribution to journal › Article
- 2005
-
Mark
Critical role for complement receptor 3 (CD11b/CD18), but not for Fc receptors, in killing of Streptococcus pyogenes by neutrophils in human immune serum.
(
- Contribution to journal › Article
-
Mark
Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: bacterial colonization may be decisive for a relationship.
(
- Contribution to journal › Article
-
Mark
Hereditary C2 Deficiency in Sweden: Frequent Occurrence of Invasive Infection, Atherosclerosis, and Rheumatic Disease.
(
- Contribution to journal › Article
- 2004
-
Mark
Induction of apoptosis in monocytes and lymphocytes by serum from patients with systemic lupus erythematosus - an additional mechanism to increased autoantigen load?
(
- Contribution to journal › Article
- 2003
-
Mark
Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency
(
- Contribution to journal › Article
-
Mark
Cystic fibrosis patients heterozygous for MASP-2 gene mutation have lowered MASP-2 concentration, without relation to clinical findings
2003) 9th European Meeting on Complement in Human Disease In Molecular Immunology 40(2-4). p.208-208(
- Contribution to journal › Published meeting abstract
-
Mark
Total C4B deficiency due to gene deletion and gene conversion in a patient with severe infections
(
- Contribution to journal › Article
-
Mark
Serologisk diagnostik vid autoimmuna sjukdomar.
2003) p.243-243(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2002
-
Mark
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
(
- Contribution to journal › Article
- 2000
-
Mark
Binding of immune complexes to erythrocyte CR1 (CD35): difference in requirement of classical pathway components and indication of alternative pathway-mediated binding in C2-deficiency
(
- Contribution to journal › Article
- 1998
-
Mark
Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon
(
- Contribution to journal › Article
-
Mark
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations
(
- Contribution to journal › Article
- 1995
-
Mark
Serum concentrations of C4 isotypes and factor B in type I C2 deficiency suggest haplotype-dependent quantitative expression of MHC class III complement genes
(
- Contribution to journal › Article
- 1988
-
Mark
Protein HC-IgA complexes carry antibody activities
(
- Contribution to journal › Article