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Wilson disease—treatment perspectives

Wilson disease (WD) is a genetic disorder caused by pathological tissue copper accumulation with secondary damage of affected organs (mainly, but not limited to, the liver and brain). The main clinical symptoms of WD are, in concordance with the pathogenesis, hepatic and/or neuropsychiatric. Current...

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Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Litwin, Tomasz, Dzieżyc, Karolina, Członkowska, Anna
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6531659/
https://ncbi.nlm.nih.gov/pubmed/31179305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2018.12.09
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