1 – 10 of 14
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2019
-
Mark
C3 glomerulopathy — understanding a rare complement-driven renal disease
2019) In Nature Reviews Nephrology(
- 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
- 2013
-
Mark
Analysis of genes coding for CD46, CD55 and C4b-binding protein in patients with idiopathic, recurrent, spontaneous pregnancy loss.
(
- Contribution to journal › Article
-
Mark
Eculizumab in an anephric patient with atypical haemolytic uraemic syndrome and advanced vascular lesions.
(
- Contribution to journal › Article
- 2012
-
Mark
A Novel C3 Mutation Causing Increased Formation of the C3 Convertase in Familial Atypical Hemolytic Uremic Syndrome.
(
- Contribution to journal › Article
- 2011
-
Mark
Complement factor I in health and disease.
(
- Contribution to journal › Article
-
Mark
Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritis
(
- Contribution to journal › Article
- 2010
-
Mark
Analysis of genes coding for CD46, CD55 and C4b-binding protein in patients with idiopathic, recurrent, spontaneous pregnancy loss
(
- Contribution to journal › Published meeting abstract
-
Mark
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
(
- Contribution to journal › Article
-
Mark
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
(
- Contribution to journal › Article