Gunnar Sturfelt (Former)
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- 2006
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Mark
Complement deficiency and disease: An update.
(
- Contribution to journal › Scientific review
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Mark
Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus
(
- 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
(
- Contribution to journal › Article
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Mark
Polyarteritis nodosa when applying the Chapel Hill nomenclature--a descriptive study on ten patients.
(
- Contribution to journal › Article
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Mark
Predictors of infusion reactions during infliximab treatment in patients with arthritis.
(
- Contribution to journal › Article
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Mark
Critical comparative analyses of anti-alpha-actinin and glomerulus-bound antibodies in human and murine lupus nephritis
(
- Contribution to journal › Article
- 2005
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Mark
Do we have blind spots in our diagnostic vision?
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- Contribution to journal › Letter
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Mark
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1
(
- Contribution to journal › Article
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Mark
Hereditary C2 Deficiency in Sweden: Frequent Occurrence of Invasive Infection, Atherosclerosis, and Rheumatic Disease.
(
- Contribution to journal › Article