Hereditary haemochromatosis is unlikely to cause movement disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-004-0445-9.pdf
Reference14 articles.
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2. Berg D, Hoggenmuller U, Hofmann E, Fischer R, Kraus M, Scheurlen M, Becker G (2000) The basal ganglia in haemochromatosis. Neuroradiology 42:9–13
3. Cammermeyer J (1947) Deposition of iron in the paraventricular areas of the human brain in hemochromatosis. J Neuropathol Exp Neurol 6:111–127
4. Demarquay G, Setiey A,Morel Y, Trepo C, Chazot G, Broussolle E (2000) Clinical Report of Three Patients With Hereditary Hemochromatosis and Movement Disorders. Mov Disord 15:1204–1209
5. Hanson EH, Imperatore G, Burke W (2001) HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology. Am J Epidemiol 154(3):193–206
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