Lillemor Melander Skattum
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- 2012
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Mark
Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation
(
- Contribution to journal › Article
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Mark
Screening for anti-factor B autoantibody in a patient with acute renal injury due to dense deposit disease.
(
- Contribution to journal › Article
- 2011
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Mark
Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations
(
- Contribution to journal › Article
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Mark
Complement deficiency states and associated infections.
(
- Contribution to journal › Article
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Mark
Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange.
(
- Contribution to journal › Article
- 2010
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Mark
Sensitive and specific assays for C3 nephritic factors permit dissection of mechanisms underlying complement dysregulation
(
- Contribution to journal › Published meeting abstract
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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
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Mark
Neutrophil degranulation and complement release in ANCA-associated vasculitis: an in vitro study
(
- Contribution to journal › Published meeting abstract
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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
- 2008
-
Mark
Complement aberrations and autoantibodies to complement proteins in relation to disease mechanisms.
(
- Thesis › Doctoral thesis (compilation)