Individualised therapeutic approach to the patient with atypical haemolytic-uraemic syndrome
Atypical haemolytic-uraemic syndrome (aHUS) is a rare disease associated with uncontrolled activation of the alternative complement pathway, leading to thrombotic microangiopathy (TMA). Early diagnosis and treatment with eculizumab, a monoclonal antibody targeting the complement component C5, are cr...
Saved in:
| Main Authors: | Ivana Mikačić, Nikolina Marić |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-11-01
|
| Series: | Clinical Medicine |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1470211824054356 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Complement-Inhibiting Therapy of Atypical Haemolytic Uremic Syndrome in a Patient With Factor H Mutation
by: Irina N. Lupan, et al.
Published: (2019-02-01) -
Kidney transplantation using complement inhibitor in a patient suffering from atypical hemolytic-uremic syndrome associated with factor H antibodies: successful prevention of recurrence of the underlying disease
by: E. I. Prokopenko, et al.
Published: (2020-07-01) -
SOLUBLE ADHESION MOLECULES IN CHILDREN WITH HEMOLYTIC UREMIC SYNDROME
by: T. E. Pankratenko, et al.
Published: (2018-12-01) -
SUCCESSFUL TREATMENT FOR ATYPICAL HEMOLYTIC UREMIC SYNDROME IN A PUERPERA
by: O. N. Ulitkina, et al.
Published: (2016-01-01) -
Real-World effectiveness of eculizumab in atypical hemolytic uremic syndrome: a retrospective study from Western China
by: Yun Hu, et al.
Published: (2025-06-01)