Cargando…
Stimulation of Liver Fibrosis by N2 Neutrophils in Wilson’s Disease
BACKGROUND & AIMS: Wilson’s disease is an inherited hepatoneurologic disorder caused by mutations in the copper transporter ATP7B. Liver disease from Wilson’s disease is one leading cause of cirrhosis in adolescents. Current copper chelators and zinc salt treatments improve hepatic presentations...
Autores principales: | Mi, Xiaoxiao, Song, Yu, Deng, Chaohua, Yan, Jian, Li, Zhihui, Li, Yingniang, Zheng, Jun, Yang, Wenjun, Gong, Ling, Shi, Junping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514429/ https://www.ncbi.nlm.nih.gov/pubmed/37406734 http://dx.doi.org/10.1016/j.jcmgh.2023.06.012 |
Ejemplares similares
-
Evaluation of liver fibrosis in patients with Wilson’s disease
por: Przybyłkowski, Adam, et al.
Publicado: (2020) -
Biliary sepsis complication with congenital hepatic fibrosis: an unexpected outcome
por: Sun, Jiawei, et al.
Publicado: (2023) -
Pediatric Wilson disease presenting as acute liver failure: Prognostic indices
por: Fang, Wei-Yuan, et al.
Publicado: (2021) -
Elastography of the Liver in Wilson’s Disease
por: Nehring, Piotr, et al.
Publicado: (2023) -
Dr. Wm. N. Wilson
por: Hamilton, Frank A.
Publicado: (1905)