Rutger Maas
Overview
Explore the profile of Rutger Maas including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
4
Citations
60
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Rao D, Maas R, Cornelissen M, Wetzels J, van Geel M
Nephron
. 2024 Mar;
PMID: 38547857
Alport syndrome (AS) is a hereditary kidney disorder of type IV collagen caused by pathogenic variants in the COL4A3, COL4A4 and COL4A5 genes. Previously several cases of digenic AS, caused...
2.
den Braanker D, Maas R, Parr N, Deegens J, Smeets B, Wetzels J, et al.
PLoS One
. 2022 Sep;
17(9):e0274959.
PMID: 36137166
Recurrence of proteinuria after kidney transplantation in primary focal segmental glomerulosclerosis (FSGS) is unpredictable. Several putative circulating permeability factors (CPFs) have been suggested, but none have been validated. A clinically...
3.
Gauckler P, Shin J, Alberici F, Audard V, Bruchfeld A, Busch M, et al.
Kidney Int Rep
. 2021 Apr;
6(4):881-893.
PMID: 33912740
Membranous nephropathy (MN) is the most common cause of primary nephrotic syndrome among adults. The identification of phospholipase A2 receptor (PLA2R) as target antigen in most patients changed the management...
4.
Gauckler P, Shin J, Alberici F, Audard V, Bruchfeld A, Busch M, et al.
Autoimmun Rev
. 2020 Sep;
19(11):102671.
PMID: 32942039
Primary forms of minimal change disease and focal segmental glomerulosclerosis are rare podocytopathies and clinically characterized by nephrotic syndrome. Glucocorticoids are the cornerstone of the initial immunosuppressive treatment in these...