These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 8232931)

  • 21. The genetics of primary torsion dystonia.
    Müller U; Kupke KG
    Hum Genet; 1990 Jan; 84(2):107-15. PubMed ID: 2404852
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic linkage analysis in primary torsion dystonia.
    Bressman SB; Fahn S; Falk C; Allen FH; Suciu-Foca N
    Neurology; 1984 Nov; 34(11):1490-3. PubMed ID: 6493498
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A case-control study of idiopathic torsion dystonia.
    Fletcher NA; Harding AE; Marsden CD
    Mov Disord; 1991; 6(4):304-9. PubMed ID: 1758448
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Idiopathic torsion dystonia and writing tremor within a family.
    Hayashi M; Koide H
    Brain Dev; 1997 Dec; 19(8):556-8. PubMed ID: 9440801
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular genetic analysis of essential tremor].
    Illarioshkin SN; Rakhmonov RA; Ivanova-Smolenskaia IA; Brice A; Markova ED; Miklina NI; Kliushnikov SA; Limborskaia SA
    Genetika; 2002 Dec; 38(12):1704-9. PubMed ID: 12575458
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. The genetics of idiopathic torsion dystonia.
    Fahn S
    Int J Neurol; 1991-1992; 25-26():70-80. PubMed ID: 11980065
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3.
    Norgren N; Mattson E; Forsgren L; Holmberg M
    Neurogenetics; 2011 May; 12(2):137-43. PubMed ID: 21301909
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia.
    Brancati F; Defazio G; Caputo V; Valente EM; Pizzuti A; Livrea P; Berardelli A; Dallapiccola B
    Mov Disord; 2002 Mar; 17(2):392-7. PubMed ID: 11921130
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Genetic study of idiopathic torsion dystonia in Russia].
    Dadali EL; Markova ED; Petrin AN; Ivanova-Smolenskaia IA; Okuneva EG
    Genetika; 1996 Mar; 32(3):415-9. PubMed ID: 8723633
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Variable onset of adult inherited focal dystonia: a problem for genetic studies.
    Micheli S; Fernández-Pardal M; Quesada P; Brannan T; Obeso JA
    Mov Disord; 1994 Jan; 9(1):64-8. PubMed ID: 8139606
    [No Abstract]   [Full Text] [Related]  

  • 32. Human gene for torsion dystonia located on chromosome 9q32-q34.
    Ozelius L; Kramer PL; Moskowitz CB; Kwiatkowski DJ; Brin MF; Bressman SB; Schuback DE; Falk CT; Risch N; de Leon D
    Neuron; 1989 May; 2(5):1427-34. PubMed ID: 2576373
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Primary torsion dystonia: the search for genes is not over.
    Jarman PR; del Grosso N; Valente EM; Leube B; Cassetta E; Bentivoglio AR; Waddy HM; Uitti RJ; Maraganore DM; Albanese A; Frontali M; Auburger G; Bressman SB; Wood NW; Nygaard TG
    J Neurol Neurosurg Psychiatry; 1999 Sep; 67(3):395-7. PubMed ID: 10449567
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset.
    Gasser T; Windgassen K; Bereznai B; Kabus C; Ludolph AC
    Ann Neurol; 1998 Jul; 44(1):126-8. PubMed ID: 9667600
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genomic imprinting and anticipation in idiopathic torsion dystonia.
    LaBuda MC; Fletcher NA; Korczyn AD; Inzelberg R; Harding AE; Pauls DL
    Neurology; 1993 Oct; 43(10):2040-3. PubMed ID: 8413963
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DYT1 mutation in Japanese patients with primary torsion dystonia.
    Matsumoto S; Nishimura M; Kaji R; Sakamoto T; Mezaki T; Shimazu H; Murase N; Shibasaki H
    Neuroreport; 2001 Mar; 12(4):793-5. PubMed ID: 11277585
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
    Münchau A; Valente EM; Davis MB; Stinton V; Wood NW; Quinn NP; Bhatia KP
    Mov Disord; 2000 Sep; 15(5):954-9. PubMed ID: 11009204
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
    Defazio G; Brancati F; Valente EM; Caputo V; Pizzuti A; Martino D; Abbruzzese G; Livrea P; Berardelli A; Dallapiccola B
    Mov Disord; 2003 Feb; 18(2):207-12. PubMed ID: 12539217
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Intrafamilial correlation in idiopathic torsion dystonia.
    Fletcher NA; Harding AE; Marsden CD
    Mov Disord; 1991; 6(4):310-4. PubMed ID: 1758449
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Tiapride as treatment for certain patients with idiopathic torsion dystonia.
    Arlazoroff A; Klein C; Meiner Z; Milo R; Theitler J; Carpel CL
    Eur Neurol; 1991; 31(6):356-9. PubMed ID: 1756758
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.