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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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Detaylı Bibliyografya
Yayımlandı:Turk Pediatri Ars
Asıl Yazarlar: Bayram, Ayşe Kaçar, Gümüş, Hakan, Arslan, Duran, Özçora, Güldemet Kaya, Kumandaş, Sefer, Karacabey, Neslihan, Canpolat, Mehmet, Per, Hüseyin
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Turkish Pediatrics Association 2016
Konular:
Online Erişim: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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