The pathophysiology of Wilson’s disease visualized: A human (64)Cu PET study

BACKGROUND AND AIMS: Wilson’s disease (WD) is a genetic disease with systemic accumulation of copper that leads to symptoms from the liver and brain. However, the underlying defects in copper transport kinetics are only partly understood. We sought to quantify hepatic copper turnover in patients wit...

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Detalles Bibliográficos
Autores principales: Sandahl, Thomas Damgaard, Gormsen, Lars C., Kjærgaard, Kristoffer, Vendelbo, Mikkel Holm, Munk, Ditte Emilie, Munk, Ole Lajord, Bender, Dirk, Keiding, Susanne, Vase, Karina H., Frisch, Kim, Vilstrup, Hendrik, Ott, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305563/
https://www.ncbi.nlm.nih.gov/pubmed/34773664
http://dx.doi.org/10.1002/hep.32238

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305563/
https://www.ncbi.nlm.nih.gov/pubmed/34773664
http://dx.doi.org/10.1002/hep.32238

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