Expression of activin A in liver tissue and the outcome of patients with biliary atresia
Biliary atresia (BA) is a rare disease of unknown etiology which leads to cirrhosis and death if left untreated. The standard of care is an early hepatoportoenterostomy (HPE). Long-term follow-up is mandatory, during which most patients will require a liver transplant. Activin A belongs to the trans...
Saved in:
| Main Authors: | Petra Džepina, Marijana Ćorić, Matea Kovačić Perica, Mirna Natalija Aničić, Ruža Grizelj, Jurica Vuković |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2024-11-01
|
| Series: | Frontiers in Pediatrics |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2024.1457837/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Identification of clinical and laboratory factors predictive of long term-native liver survival after Kasai portoenterostomy
by: Takashi Kobayashi, et al.
Published: (2025-07-01) -
ETIOLOGY, PATHOGENESIS AND MORPHOLOGY OF BILIARY ATRESIA
by: O. E. Iryshkin, et al.
Published: (2012-09-01) -
Prevalence of liver disorders in children and adolescents with type 1 diabetes mellitus
by: Mirna Natalija Anicic, et al.
Published: (2025-08-01) -
Structural Disruption of Cilia and Increased Cytoplasmic Tubulin in Biliary Atresia—An Exploratory Study Focusing on Early Postoperative Prognosis Following Portoenterostomy
by: Patrícia Quelhas, et al.
Published: (2025-01-01) -
Three decades of progress: evolution of outcomes and prognostic indicators in biliary atresia management
by: Senol Emre, et al.
Published: (2025-07-01)