Treatment options in Huntington's disease

Neuroacanthocytosis Syndromes

Volumn , Issue , 2005, Pages 243-250

  Dose, Matthias ^a  

^a Bezirkskrankenhaus Taufkirchen ^*  (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 70349705183     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/1-4020-2898-9_27     Document Type: Chapter

References (23)

1. Bachoud-Levi AC, Remy P, Nguyen JP et al (2000) Motor and cognitive improvements in patients with Huntington's disease after neural transplantation. Lancet 356:1975-1979.
2. Bauer P, Knoblich R, Mix E, Pahnke J, Rolfs A (2002) Aktueller Stand und Perspektive der Zelltransplantation bei neurodegenerativen Erkrankungen. Nervenheilkunde 21:88-93.
3. Davenport CB, Muncey EB (1916) Huntington's chorea in relation to heredity and eugenics. Eugenics Record Office Bulletin 17:195-222.
4. Di Figlia M, Sapp E, Chase KO, Davies SW, Bates GP, Vonsattel JP, Aronin N (1997) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science 277:1990-1993.
5. Dose M (1997) Klinische Diagnostik und Therapie bei Anlageträgern der Huntington-Krankheit. Medizinische Genetik 9:570-579.
6. Flint-Beal M et al (2001) Novel therapies in the search for a cure for Huntington's disease. Proc Natl Acad Sci USA 98:3-4.
7. Freed CR, Greene PE, Breeze RE et al (2001) Transplantation of embryonic dopamine neurons for severe Parkinson's disease. New Engl J Med 344:710-719.
8. Gervais FG et al (2002) Recruitment and activation of caspase-8 by the Huntingtoninteracting protein Hip-1 and a novel partner Hippi. Nat Cell Biol 4:95-105.
9. Harper P (1991) Huntington's Disease. Saunders, London
10. Hughes RE, Olson JM (2001) Therapeutic opportunities in polyglutamine diseases. Nature Med 4:419-423.
11. Huntington G (1872) On chorea. Medical and Surgical Reporter 26:320-321.
12. Hoffmann J (1888) Über Chorea chronica progressiva (Huntington'sche Chorea, Chorea hereditaria). Virchows Archiv 111:513-548.
13. Klee E (1983) "Euthanasie" im NS-Staat. Fischer, Frankfurt/Main
14. Maat-Schieman ML, Dorsman JC, Smoor MA, Siesling S et al (1999) Distribution of inclusions in neuronal nuclei and dystrophic neurites in Huntington's disease brain. J Neuropathol Exp Neurol 58:129-137.
15. Phelps RM (1892) A new consideration of hereditary chorea. J Nervous Mental Dis 19:765-776.
16. Punnett RC (1908) Mendelian inheritance in man. Proc Royal Soc Med 1:135-168.
17. Rosenblatt A, Margolis RL, Becher MW et al (1998) Does CAG repeat number predict the rate of pathological changes in Huntington's disease? Ann Neurol 44:708-709.
18. Saudou F, Finkbeiner S, Devys D, Greenberg ME (1998) Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell 95:55-66.
19. Siesling S, Van Vugt JP, Roos RA (1997) Hypokinesia: A prominent feature in Huntington's disease. Kinesis 2:17-22.
20. The Huntington's Disease Collaborative Study Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983.
21. Weindl A, Ceballos-Baumann AO (2001) Chorea. In: Neurologische Therapie. Lehmann-Horn F, Ludolph H (eds) Urban und Fischer, MÜnchen, 126-149
22. Westphal C (1883) Über eine dem Bilde der cerebrospinalen grauen Degeneration ähnliche Erkrankung des zentralen Nervensystems ohne anatomischen Befund, nebst einigen Bemerkungen Über paradoxe Kontraktion. Arch Psychiatr Nervenkrankh 14:87-96; 767-773.
23. World Federation of Neurology Research Group on Huntington's Disease (1989) Ethical issues policy statement on Huntington's disease molecular predicitive test. J Neurol Sci 94:327-332.