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Neurological features and management of Wilson disease in children: an evaluation of 12 cases

AIM: Wilson’s disease is an autosomal recessive disorder of copper metabolism which leads to copper overload in different tissues of the body. The aim of this study was to present the neurologic features of Wilson’s disease and to assess the clinical course of neurological findings in children recei...

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Detalhes bibliográficos
Publicado no:Turk Pediatri Ars
Main Authors: Bayram, Ayşe Kaçar, Gümüş, Hakan, Arslan, Duran, Özçora, Güldemet Kaya, Kumandaş, Sefer, Karacabey, Neslihan, Canpolat, Mehmet, Per, Hüseyin
Formato: Artigo
Idioma:Inglês
Publicado em: Turkish Pediatrics Association 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4829162/
https://ncbi.nlm.nih.gov/pubmed/27103860
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2016.3080
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