Wilson disease in Northern Portugal: a long-term follow-up study

INTRODUCTION: Wilson disease is an autosomal recessive disease of liver copper metabolism with predominant hepatic and neurological manifestations. Long-term data on the clinical follow-up and treatment efficacy are limited due to the low frequency of the disease. We evaluated a large cohort of Wils...

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Detalles Bibliográficos
Autores principales: Garrido, Isabel, Marques, Margarida, Liberal, Rodrigo, Cardoso, Hélder, Lopes, Susana, Macedo, Guilherme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867740/
https://www.ncbi.nlm.nih.gov/pubmed/35197085
http://dx.doi.org/10.1186/s13023-022-02245-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867740/
https://www.ncbi.nlm.nih.gov/pubmed/35197085
http://dx.doi.org/10.1186/s13023-022-02245-5

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