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 *

120 related articles for article (PubMed ID: 11487218)

  • 41. A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.
    Lin Y; Liu T; Li J; Yang J; Du Q; Wang J; Yang Y; Liu X; Fan Y; Lu F; Chen Y; Pu Y; Zhang K; He X; Yang Z
    Mol Vis; 2008 Apr; 14():739-44. PubMed ID: 18432317
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Phenotypic differences in Dyt1 between ethnic groups.
    Lee WW; Ahn TB; Chung SJ; Jeon BS
    Curr Neurol Neurosci Rep; 2012 Aug; 12(4):341-7. PubMed ID: 22622408
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.
    Ozelius LJ; Kramer PL; de Leon D; Risch N; Bressman SB; Schuback DE; Brin MF; Kwiatkowski DJ; Burke RE; Gusella JF
    Am J Hum Genet; 1992 Mar; 50(3):619-28. PubMed ID: 1347197
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Evidence for locus heterogeneity in autosomal dominant torsion dystonia.
    Ahmad F; Davis MB; Waddy HM; Oley CA; Marsden CD; Harding AE
    Genomics; 1993 Jan; 15(1):9-12. PubMed ID: 8432555
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia (DYT1) - pathophysiological consideration.
    Nomura Y; Ikeuchi T; Tsuji S; Segawa M
    Brain Dev; 2000 Sep; 22 Suppl 1():S92-101. PubMed ID: 10984667
    [TBL] [Abstract][Full Text] [Related]  

  • 46. No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystonia.
    Tuffery-Giraud S; Cavalier L; Roubertie A; Guittard C; Carles S; Calvas P; Echenne B; Coubes P; Claustres M
    J Med Genet; 2001 Oct; 38(10):E35. PubMed ID: 11584049
    [No Abstract]   [Full Text] [Related]  

  • 47. Dystonia: phenotypes and genotypes.
    Bressman SB
    Rev Neurol (Paris); 2003 Oct; 159(10 Pt 1):849-56. PubMed ID: 14628853
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family.
    Kabakci K; Isbruch K; Schilling K; Hedrich K; de Carvalho Aguiar P; Ozelius LJ; Kramer PL; Schwarz MH; Klein C
    J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):860-2. PubMed ID: 15897512
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The genetics of primary dystonias and related disorders.
    Németh AH
    Brain; 2002 Apr; 125(Pt 4):695-721. PubMed ID: 11912106
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE; Ritch R; Lichter PR; Rozsa FW; Stringham HM; Caronia RM; Johnson D; Abundo GP; Willcockson J; Downs CA; Thompson DA; Musarella MA; Gupta N; Othman MI; Torrez DM; Herman SB; Wong DJ; Higashi M; Boehnke M
    Ophthalmology; 1998 Sep; 105(9):1698-707. PubMed ID: 9754180
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.
    Johnson AT; Richards JE; Boehnke M; Stringham HM; Herman SB; Wong DJ; Lichter PR
    Ophthalmology; 1996 May; 103(5):808-14. PubMed ID: 8637692
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Striatal dopamine in early-onset primary torsion dystonia with the DYT1 mutation.
    Furukawa Y; Hornykiewicz O; Fahn S; Kish SJ
    Neurology; 2000 Mar; 54(5):1193-5. PubMed ID: 10720299
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical and genetic evaluation in a French population presenting with primary focal dystonia.
    Dhaenens CM; Krystkowiak P; Douay X; Charpentier P; Bele S; Destée A; Sablonnière B
    Mov Disord; 2005 Jul; 20(7):822-5. PubMed ID: 15726581
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis.
    Kupke KG; Lee LV; Müller U
    Neurology; 1990 Sep; 40(9):1438-42. PubMed ID: 1975433
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic and clinical features of primary torsion dystonia.
    Ozelius LJ; Bressman SB
    Neurobiol Dis; 2011 May; 42(2):127-35. PubMed ID: 21168499
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.