Anders Sjöholm (Former)
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- 2009
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Mark
Genetic, molecular and functional analyses of complement factor I deficiency.
(
- Contribution to journal › Article
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Mark
Human complement activation by smooth and rough Proteus mirabilis lipopolysaccharides
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- Contribution to journal › Article
- 2008
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Mark
Genetic analysis of complement C1s deficiency associated with systemic lupus erythernatosus highlights alternative splicing of normal C1s gene
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- Contribution to journal › Article
- 2007
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Mark
Design of recombinant antibody microarrays for serum protein profiling: Targeting of complement proteins
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- Contribution to journal › Article
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Mark
C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations
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- Contribution to journal › Article
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Mark
Rheumatological manifestations, organ damage and autoimmunity in hereditary C2 deficiency.
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- Contribution to journal › Article
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Mark
Cooperation between MASP-1 and MASP-2 in the generation of C3 convertase through the MBL pathway
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- Contribution to journal › Article
- 2006
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Mark
Mannan-binding lectin activates C3 and the alternative complement pathway without involvement of C2.
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- Contribution to journal › Article
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Mark
Complement deficiency and disease: An update.
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- Contribution to journal › Scientific review
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Mark
Properdin deficiency in a boy with fulminant meningococcal septic shock
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- Contribution to journal › Article
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Mark
Influence of methotrexate, TNF blockers and prednisolone on antibody responses to pneumococcal polysaccharide vaccine in patients with rheumatoid arthritis.
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- Contribution to journal › Article
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Mark
Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.
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- Contribution to journal › Article
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Mark
Homozygosity for the IgG2 subclass allotype G2M(n) protects against severe infection in hereditary C2 deficiency
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- Contribution to journal › Article
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Mark
Antibodies against Four Proteins from a Streptococcus pyogenes Serotype M1 Strain and Levels of Circulating Mannan-Binding Lectin in Acute Poststreptococcal Glomerulonephritis.
(
- Contribution to journal › Article
- 2005
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Mark
Hereditary C2 Deficiency in Sweden: Frequent Occurrence of Invasive Infection, Atherosclerosis, and Rheumatic Disease.
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- Contribution to journal › Article
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Mark
Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: bacterial colonization may be decisive for a relationship.
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- Contribution to journal › Article
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Mark
Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis
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- Contribution to journal › Article
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Mark
Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA
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- Contribution to journal › Article
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Mark
Factor H binds to washed human platelets
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- Contribution to journal › Article
- 2003
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Mark
Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency
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- Contribution to journal › Article
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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
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Mark
Inherited deficiency of mannan-binding lectin-associated serine protease 2
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- Contribution to journal › Article
- 2002
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Mark
A hemolytic assay for the estimation of functional mannose-binding lectin levels in human serum
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- Contribution to journal › Article
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Mark
EndoS and SpeB from Streptococcus pyogenes inhibit immunoglobulin-mediated opsonophagocytosis.
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- Contribution to journal › Article
- 2000
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Mark
Novel roles of complement in systemic lupus erythematosus - Hypothesis for a pathogenetic vicious circle
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- Contribution to journal › Article
- 1998
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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
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- Contribution to journal › Article
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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
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- Contribution to journal › Article
- 1997
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Mark
Hypocomplementemia caused by C3 nephritic factors (C3 NeF): clinical findings and the coincidence of C3 NeF type II with anti-C1q autoantibodies.
(
- Contribution to journal › Article