Reversible Huntington's disease?

Lancet

Volumn 352, Issue 9139, 1998, Pages 1520-1521

  Bonelli, Raphael ^a   Költringer, Peter ^b   Kenner, Lukas ^b   Reisecker, Franz ^b  

^a Hospital BHB Eggenberg   (Austria)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; HUMAN; HUNTINGTON CHOREA; MALE; PRIORITY JOURNAL;

EID: 0032494725     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)60326-1     Document Type: Article

References (5)

1. 1 The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993; 72: 971-83.
2. 2 Westphal C. Über eine dem Bilde der cerebrospinalen grauen Degeneration ähnlichen Erkrankung des centralen Nervensystems ohne anatomischen Befund, nebst einigen Bemerkungen über paradoxe Contraktionen. Arch Pyschiatr Nervenkr 1883; 14: 187-234.
3. 3 Nivelon-Chvallier A, Giround M, Fabre JL, et al. Effect of metoclopramide in a subject at risk of Huntington's chorea. J Genet Hum 1985; 33: 131-33.
4. 4 Barr AN, Fischer JH, Koller WC, et al. Serum haloperidol concentration and choreiform movements in Huntington's disease. Neurology 1988; 38: 84-88.
5. 5 Davis MB, Bateman D, Quinn NP, et al. Mutation analysis with possible but apparent sporadic Huntington's disease. Lancet 1994; 344: 714-17.