Genetics in movement disorders: Dystonia, tremor and chorea;Genetikk ved bevegelsesforstyrrelser - Dystoni, tremor og chorea

Tidsskrift for den Norske Laegeforening

Volumn 124, Issue 17, 2004, Pages 2236-2237

  Dietrichs, Espen ^a   Tallaksen, Chantal M E ^b  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CHOREA; DYSTONIA; ESSENTIAL TREMOR; GENETIC COUNSELING; GENETIC DISORDER; GENETIC HETEROGENEITY; HUMAN; HUNTINGTON CHOREA; MOTOR DYSFUNCTION; PATHOGENESIS; REVIEW; TREMOR; GENETICS; PHENOTYPE;

DYSTONIC DISORDERS; ESSENTIAL TREMOR; GENETIC COUNSELING; HUMANS; HUNTINGTON DISEASE; PHENOTYPE;

EID: 4644302959     PISSN: 00292001     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (20)

1. Toft M, Aasly J. Genetikk ved Parkinsons sykdom. Tidsskr Nor Lasgeforen 2004; 124: 922-4.
2. Tallaksen CME, Dietrichs E. Genetikk ved bevegelsesforstyrrelser - spinocerebellære lidelser. Tidsskr Nor Lægeforen 2004; 124: 2233-5.
3. Nutt JG, Muenter MD, Aronson A et al. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord 1988; 3: 188-94.
4. Le K-D, Nilsen B, Dietrichs E. Prevalence of primary focal and segmental dystonia in Oslo. Neurology 2003; 61: 1294-6.
5. Risch N, deLeon D, Ozelius L et al. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. Am J Human Genet 1995; 9: 152-9.
6. Bressman SB, Sabatti C, Raymond D et al. The DYT1 phenotype and guidelines for diagnostic testing. Neurology 2000; 54: 1746-52.
7. Farbu E, Bindoff LA. Doparesponsiv dystoni - en arvelig dystoni som er lett å behandle. Tidsskr Nor Lasgeforen 2002; 122: 379-81.
8. Aguiar PM, Ozelius LJ. Classification and genetics of dystonia. Lancet Neurol 2002; 1: 316-25.
9. Solano A, Roig M, Vives-Baza C et al. Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene. Ann Neurol 2003; 54: 527-30.
10. Lund JC. Chorea St. Viti i Sætersdalen. Beretning om Sundhetstilstanden m.m. i Norge, 1860: 137-8.
11. Folstein SE, Chase GA, Wahl WE et al. Huntington's disease in Maryland: clinical aspects and racial variation. Am J Hum Genet 1987; 41: 168-79.
12. SuttonBrown M, Suchowersky O. Clinical and research advances in Huntington's disease. Can J Neurol Sci 2003; 30 (suppl 1): 45-52.
13. Zuhlke C, Riess O, Bockel B et al. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington's disease gene. Hum Mol Genet 1993; 2: 2063-7.
14. Louis ED, Fried LP, Fitzpatrick AL et al. Regional and racial differences in the prevalences of physician diagnosed essential tremor in the United States. Mov Disord 2003; 18: 1035-40.
15. Sethi KD. Tremor. Curr Opin Neurol 2003; 16: 481-5.
16. Helle JR, Braathen GJ. Skodje T et al. Diagnostisk DNA testing for Huntingtons sykdom. Tidsskr Nor Lægeforen 2000; 120: 2408-10.
17. Helle JR, Braathen GJ, Pedersen JC et al. Genetisk veiledning ved presymptomatisk testing for Huntingtons sykdom. Tidsskr Nor Lægeforen 2000; 120: 2412-6.
18. Kerty E, Gjerstad L, Nyberg-Hansen R. Botulinumtoksinbehandling av spastisk torticollis. Tidsskr Nor Lægeforen 1992; 112: 2660-2
19. Lozano AM, Abosch A. Pallidal stimulation for dystonia. Adv Neurol 2004; 94: 301-8.
20. Vaillancourt DE, Sturman MM, Verhagen Metman L et al. Deep brain stimulation of the VIM thalamic nucleus modifies several features of essential tremor. Neurology 2003; 61: 919-25.