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Journal Abstract Search

278 related items for PubMed ID: 11980065

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

  • 22. Linkage analysis in British and French families with idiopathic torsion dystonia.
    Warner TT, Fletcher NA, Davis MB, Ahmad F, Conway D, Feve A, Rondot P, Marsden CD, Harding AE.
    Brain; 1993 Jun; 116 ( Pt 3)():739-44. PubMed ID: 8513401
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Temporal discrimination threshold: VBM evidence for an endophenotype in adult onset primary torsion dystonia.
    Bradley D, Whelan R, Walsh R, Reilly RB, Hutchinson S, Molloy F, Hutchinson M.
    Brain; 2009 Sep; 132(Pt 9):2327-35. PubMed ID: 19525326
    [Abstract] [Full Text] [Related]

  • 25. Functional brain networks in DYT1 dystonia.
    Eidelberg D, Moeller JR, Antonini A, Kazumata K, Nakamura T, Dhawan V, Spetsieris P, deLeon D, Bressman SB, Fahn S.
    Ann Neurol; 1998 Sep; 44(3):303-12. PubMed ID: 9749595
    [Abstract] [Full Text] [Related]

  • 26. Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystonia.
    Gambarin M, Valente EM, Liberini P, Barrano G, Bonizzato A, Padovani A, Moretto G, Fiorio M, Dallapiccola B, Smania N, Fiaschi A, Tinazzi M.
    Mov Disord; 2006 Oct; 21(10):1782-4. PubMed ID: 16874761
    [Abstract] [Full Text] [Related]

  • 27. Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.
    Kwiatkowski DJ, Ozelius L, Kramer PL, Perman S, Schuback DE, Gusella JF, Fahn S, Breakefield XO.
    Am J Hum Genet; 1991 Aug; 49(2):366-71. PubMed ID: 1867195
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. 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 Feb; 4(5):377-86. PubMed ID: 3692135
    [Abstract] [Full Text] [Related]

  • 30. A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.
    Bressman SB, Heiman GA, Nygaard TG, Ozelius LJ, Hunt AL, Brin MF, Gordon MF, Moskowitz CB, de Leon D, Burke RE.
    Neurology; 1994 Feb; 44(2):283-7. PubMed ID: 8309575
    [Abstract] [Full Text] [Related]

  • 31. Sporadic adult onset primary torsion dystonia is a genetic disorder by the temporal discrimination test.
    Kimmich O, Bradley D, Whelan R, Mulrooney N, Reilly RB, Hutchinson S, O'Riordan S, Hutchinson M.
    Brain; 2011 Sep; 134(Pt 9):2656-63. PubMed ID: 21840890
    [Abstract] [Full Text] [Related]

  • 32. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium.
    Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO.
    Genome Res; 1997 May; 7(5):483-94. PubMed ID: 9149944
    [Abstract] [Full Text] [Related]

  • 33. [Molecular-genetic analysis of torsion dystonia in Russia].
    Markova ED, Slominskiĭ PA, Illarioshkin SN, Miklina NI, Shadrina MI, Popova SN, Limborskaia SA, Ivanova-Smolenskaia IA.
    Genetika; 2000 Jul; 36(7):952-8. PubMed ID: 10994500
    [Abstract] [Full Text] [Related]

  • 34. Inherited and de novo mutations in sporadic cases of DYT1-dystonia.
    Hjermind LE, Werdelin LM, Sørensen SA.
    Eur J Hum Genet; 2002 Mar; 10(3):213-6. PubMed ID: 11973627
    [Abstract] [Full Text] [Related]

  • 35. Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.
    Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S.
    Mol Psychiatry; 2008 Apr; 13(4):442-50. PubMed ID: 17579605
    [Abstract] [Full Text] [Related]

  • 36. Defective temporal processing of sensory stimuli in DYT1 mutation carriers: a new endophenotype of dystonia?
    Fiorio M, Gambarin M, Valente EM, Liberini P, Loi M, Cossu G, Moretto G, Bhatia KP, Defazio G, Aglioti SM, Fiaschi A, Tinazzi M.
    Brain; 2007 Jan; 130(Pt 1):134-42. PubMed ID: 17105745
    [Abstract] [Full Text] [Related]

  • 37. Linkage analysis with chromosome 9 markers in hereditary essential tremor.
    Conway D, Bain PG, Warner TT, Davis MB, Findley LJ, Thompson PD, Marsden CD, Harding AE.
    Mov Disord; 1993 Jul; 8(3):374-6. PubMed ID: 8341306
    [Abstract] [Full Text] [Related]

  • 38. Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
    Valente EM, Povey S, Warner TT, Wood NW, Davis MB.
    Ann Hum Genet; 1999 Jan; 63(Pt 1):1-8. PubMed ID: 10738516
    [Abstract] [Full Text] [Related]

  • 39. Laterality of onset in idiopathic torsion dystonia.
    Inzelberg R, Zilber N, Kahana E, Korczyn AD.
    Mov Disord; 1993 Jul; 8(3):327-30. PubMed ID: 8341297
    [Abstract] [Full Text] [Related]

  • 40. Genetics, geography and intelligence in the torsion dystonias.
    Eldridge R, Edgar A, Cooper IS.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):167-77. PubMed ID: 5173357
    [Abstract] [Full Text] [Related]

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