WCN24-1884 THROMBOTIC MICROANGIOPATHY, SYSTEMIC LUPUS ERYTHEMATOSUS, AND A VITAMIN B12 MUTATION: A CAUSE OF PRIMARY ATYPICAL HEMOLYTIC UREMIC SYNDROME?
Saved in:
| Main Authors: | Jose Heriberto Díaz Góngora, Hernan Trimarchi, Mariano Forrester, Sandra Liliana Borda, Mariana Ursino, Matias Monkowski, Mauro Lampo |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-04-01
|
| Series: | Kidney International Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2468024924011781 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
WCN24-1780 A TEN-YEAR EXPERIENCE OF ATYPICAL HEMOLYTIC UREMIC SYNDROME: A MONOCENTRIC PROSPECTIVE EXPERIENCE
by: Mariana Ursino, et al.
Published: (2024-04-01) -
Ten tips for managing complement-mediated thrombotic microangiopathies (formerly atypical hemolytic uremic syndrome): narrative review
by: Pilar Musalem
Published: (2025-03-01) -
Atypical hemolytic uremic syndrome: a case report and review of thrombotic mechanisms
by: George N. Zsidisin
Published: (2025-04-01) -
WCN24-1921 NEPHROTIC SYNDROME SECONDARY AND FOCAL SEGMENTAL GLOMERULOSCLEROSIS DUE TO PODOCYTE KANK-2 MUTATION
by: Sandra Liliana Borda Galindo, et al.
Published: (2024-04-01) -
Ex vivo C5b-9 Deposition Test to Monitor Complement Activity in Clinical and Subclinical Atypical Hemolytic Uremic Syndrome and in Transplantation-Associated Thrombotic Microangiopathy
by: Maria Martin, et al.
Published: (2024-07-01)