Sleep Abnormalities in Wilson’s Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
http://link.springer.com/article/10.1007/s11940-018-0531-4/fulltext.html
Reference48 articles.
1. Tanzi R, Petrukhin K, Chernov I, et al. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat Genet. 1993;3:344–50.
2. • Woimant F, Trocello J-M. Disorders of heavy metals. Elsevier, editor. Handb Clin Neurol. 2014;120:851–64. Insightful review of the current clinical, diagnostic, and treatment challenges in heavy metal disorders.
3. Poujois A, Woimant F. Wilson’s disease: a 2017 update. Clin Res Hepatol Gastroenterol 2018 (in press).
4. Biswas S, Paul N, Das SK. Nonmotor manifestations of Wilson’s disease. Int Rev Neurobiol. 2017;134:1443–59.
5. Giagheddu M, Tamburini G, Piga M, Tacconi P, Giagheddu A, Serra A, et al. Comparison of MRI, EEG, EPs and ECD-SPECT in Wilson’s disease. Acta Neurol Scand. 2001;103:71–81.
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