Chorea-acanthocytosis Neurological disease with acanthocytosis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1983.tb04815.x/fullpdf
Reference22 articles.
1. Malformation of the erythrocytes in a case of atypical retinitis pigmentosa;Bassen;Blood,1959
2. Quantitative chromatographic analysis of plasma and red blood cell lipids in patients with acanthocytosis;Phillips;J Lab Clin Med,1962
3. Congenital betalipoprotein deficiency: an hereditary disorder involving a defect in the absorption and transport of lipids;Isselbacher;Medicine (Baltim),1964
4. Hemolysis and changes in erythrocyte membrane lipids;Shohet;N Engl J Med,1972
5. Familial hypobetalipoproteinemia. A genetic disorder of lipid metabolism with nervous system involvement;Mars;Am J Med,1969
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1. Movement disorders of the mouth: a review of the common phenomenologies;Journal of Neurology;2022-07-29
2. ELECTROMYOGRAPHIG FINDINGS IN CHOREA-ACANTHOCYTOSIS;Acta Neurologica Scandinavica;2009-01-29
3. Autonomic Dysfunction in Neuroacanthocytosis and Causes of Sudden Death: Analysis of a Case of Chorea-Acanthocytosis with Dysautonomia;Neuroacanthocytosis Syndromes II;2008
4. Familial Temporal Lobe Epilepsy as a Presenting Feature of Choreoacanthocytosis;Epilepsia;2005-08
5. Neuroacanthocytosis;American Journal of Psychiatry;2004-09
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