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- 2006
-
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