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- 2023
-
Mark
Complement-mediated kidney diseases: Genotype, phenotype and inhibition studies
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome
(
- Contribution to journal › Article
- 2022
-
Mark
Aspects of Complement Activation in Thrombocytopenic Disorders
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome
(
- Contribution to journal › Article
- 2021
-
Mark
Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis
(
- Contribution to journal › Article
- 2020
-
Mark
Functional Assessment of Fatigue and Other Patient-Reported Outcomes in Patients Enrolled in the Global aHUS Registry
(
- Contribution to journal › Article
- 2018
-
Mark
Overactivity of alternative pathway convertases in patients with complement-mediated renal diseases
(
- Contribution to journal › Article
- 2017
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Mark
Orphan drug policies and use in pediatric nephrology
(
- Contribution to journal › Debate/Note/Editorial
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Mark
At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome : A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature
(
- Contribution to journal › Scientific review
- 2016
-
Mark
An international consensus approach to the management of atypical hemolytic uremic syndrome in children
(
- Contribution to journal › Scientific review