Neuroacanthocytosis

Practical Neurology

Volumn 4, Issue 5, 2004, Pages 298-301

  Zeman, Adam ^a   Shenton, Geoff ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b WESTERN GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ABETALIPOPROTEINEMIA; ACANTHOCYTOSIS; ADULT; AREFLEXIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BEHAVIOR DISORDER; CASE REPORT; CHOREOATHETOSIS; COMPUTER ASSISTED TOMOGRAPHY; GENE MUTATION; HUMAN; HYPOBETALIPOPROTEINEMIA; MALE; MUSCLE ATROPHY; NEUROLOGIC DISEASE; NEUROLOGIC EXAMINATION; PATHOPHYSIOLOGY; SLEEP DISORDER;

EID: 7244247052     PISSN: 14747758     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1474-7766.2004.00249.x     Document Type: Article

References (5)

1. Cummings JL (1993) Frontal-subcortical circuits and human behaviour. Archives of Neurology, 30, 873-80.
2. Danek A, Rubin JP, Rampoldi L et al. (2001) McLeod Neuroacanthocytosis: genotype and phenotype. Annals of Neurology, 50, 755-64.
3. Rampoldi L, Danek A & Monaco AP (2002) Clinical features and molecular basis of neuroacanthocytosis. Journal of Molecular Medicine 80, 475-91.
4. Stevenson VL & Hardie RJ (2001) Acanthocytosis and neurological disorders. Journal of Neurology, 248, 87-94.
5. Walker RH, Morgello S, Davidoff-Feldman B et al. (2002) Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions. Neurology, 58, 1031-7.