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- 2020
-
Mark
Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies
(
- Contribution to journal › Article
- 2019
-
Mark
Analysis of anti-C1q autoantibodies by western blot
(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2018
-
Mark
Inherited Classical and Alternative Pathway Complement Deficiencies in Children : A Single Center Experience
(
- Contribution to journal › Article
- 2015
-
Mark
Heat differentiated complement factor profiling.
(
- Contribution to journal › Article
- 2014
-
Mark
Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings.
(
- Contribution to journal › Article
- 2012
-
Mark
Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation
(
- Contribution to journal › Article
- 2011
-
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
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