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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...
Tallennettuna:
| Julkaisussa: | Turk Pediatri Ars |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Turkish Pediatrics Association
2016
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| Aiheet: | |
| Linkit: | 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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