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3. The neuropharmacology of tardive dyskinesia, spontaneous dyskinesia, and other dystonias. Stahl SM; Davis KL; Berger PA J Clin Psychopharmacol; 1982 Oct; 2(5):321-8. PubMed ID: 6127351 [TBL] [Abstract][Full Text] [Related]
4. Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion. Quinn NP; Rothwell JC; Thompson PD; Marsden CD Adv Neurol; 1988; 50():391-401. PubMed ID: 3400498 [No Abstract] [Full Text] [Related]
5. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis. Kramer PL; Ozelius L; Gusella JF; Fahn S; Kidd KK; Breakefield XO Genet Epidemiol; 1987; 4(5):377-86. PubMed ID: 3692135 [TBL] [Abstract][Full Text] [Related]
6. [Symposium on diseases of the basal ganglia. Nature of dystonia. I]. Denny-Brown D Rev Bras Med; 1968 Nov; 25(11):769-73 contd. PubMed ID: 5720951 [No Abstract] [Full Text] [Related]
7. Update on the genetics of primary torsion dystonia loci DYT6, DYT7, and DYT13 and the dystonia-plus locus DYT12. Ozelius LJ Adv Neurol; 2004; 94():109-12. PubMed ID: 14509662 [No Abstract] [Full Text] [Related]
8. Tardive dystonia. Kang UJ; Burke RE; Fahn S Adv Neurol; 1988; 50():415-29. PubMed ID: 3400500 [TBL] [Abstract][Full Text] [Related]
9. Exclusion of the DYT1 locus in familial torticollis. Bressman SB; Warner TT; Almasy L; Uitti RJ; Greene PE; Heiman GA; Raymond D; Ford B; de Leon D; Fahn S; Kramer PL; Risch NJ; Maraganore DM; Nygaard TG; Harding AE Ann Neurol; 1996 Oct; 40(4):681-4. PubMed ID: 8871591 [TBL] [Abstract][Full Text] [Related]
12. Hereditary progressive dystonia with marked diurnal fluctuation--consideration on its pathophysiology based on the characteristics of clinical and polysomnographical findings. Segawa M; Nomura Y; Tanaka S; Hakamada S; Nagata E; Soda M; Kase M Adv Neurol; 1988; 50():367-76. PubMed ID: 3041759 [No Abstract] [Full Text] [Related]
13. Dystonia musculorum deformans--a status report. Menkes JH Bull Los Angeles Neurol Soc; 1976 Oct; 41(4):184-8. PubMed ID: 23190 [No Abstract] [Full Text] [Related]
15. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol. Klein C; Pramstaller PP; Castellan CC; Breakefield XO; Kramer PL; Ozelius LJ Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609 [TBL] [Abstract][Full Text] [Related]
16. [Genetic dissection of dystonia]. Tamiya G No To Shinkei; 2005 Nov; 57(11):935-44. PubMed ID: 16363633 [No Abstract] [Full Text] [Related]
17. Late onset rest-tremor in DYT1 dystonia. Stamelou M; Edwards MJ; Bhatia KP Parkinsonism Relat Disord; 2013 Jan; 19(1):136-7. PubMed ID: 22721973 [No Abstract] [Full Text] [Related]
18. Abnormal low frequency drive in myoclonus-dystonia patients correlates with presence of dystonia. Foncke EM; Bour LJ; van der Meer JN; Koelman JH; Tijssen MA Mov Disord; 2007 Jul; 22(9):1299-307. PubMed ID: 17486590 [TBL] [Abstract][Full Text] [Related]
19. The hereditary dystonias: an emerging story with a twist. Korf BR Ann Neurol; 1998 Jul; 44(1):4-5. PubMed ID: 9667585 [No Abstract] [Full Text] [Related]
20. Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature. Edwards M; Wood N; Bhatia K Mov Disord; 2003 Jun; 18(6):706-11. PubMed ID: 12784278 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]