BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 12821514)

  • 1. Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation.
    Edwards MJ; Huang YZ; Wood NW; Rothwell JC; Bhatia KP
    Brain; 2003 Sep; 126(Pt 9):2074-80. PubMed ID: 12821514
    [TBL] [Abstract][Full Text] [Related]  

  • 2. One-Hz repetitive transcranial magnetic stimulation of the premotor cortex alters reciprocal inhibition in DYT1 dystonia.
    Huang YZ; Edwards MJ; Bhatia KP; Rothwell JC
    Mov Disord; 2004 Jan; 19(1):54-9. PubMed ID: 14743361
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Physiological studies in carriers of the DYT1 gene mutation.
    Rothwell JC; Edwards M; Huang YZ; Bhatia KP
    Rev Neurol (Paris); 2003 Oct; 159(10 Pt 1):880-4. PubMed ID: 14615676
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Motor deficits and hyperactivity in cerebral cortex-specific Dyt1 conditional knockout mice.
    Yokoi F; Dang MT; Mitsui S; Li J; Li Y
    J Biochem; 2008 Jan; 143(1):39-47. PubMed ID: 17956903
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers.
    Edwards MJ; Huang YZ; Mir P; Rothwell JC; Bhatia KP
    Mov Disord; 2006 Dec; 21(12):2181-6. PubMed ID: 17078060
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.
    Walter M; Bonin M; Pullman RS; Valente EM; Loi M; Gambarin M; Raymond D; Tinazzi M; Kamm C; Glöckle N; Poths S; Gasser T; Bressman SB; Klein C; Ozelius LJ; Riess O; Grundmann K
    Neurobiol Dis; 2010 May; 38(2):192-200. PubMed ID: 20053375
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression of the early-onset torsion dystonia gene (DYT1) in human brain.
    Augood SJ; Penney JB; Friberg IK; Breakefield XO; Young AB; Ozelius LJ; Standaert DG
    Ann Neurol; 1998 May; 43(5):669-73. PubMed ID: 9585364
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormal blink reflex recovery cycle in manifesting and nonmanifesting carriers of the DYT1 gene mutation.
    Fong PY; Edwards MJ; Lu CS; Chen RS; Rothwell JC; Bhatia KP; Huang YZ
    Neuroreport; 2016 Sep; 27(14):1046-9. PubMed ID: 27508977
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
    Grundmann K; Laubis-Herrmann U; Bauer I; Dressler D; Vollmer-Haase J; Bauer P; Stuhrmann M; Schulte T; Schöls L; Topka H; Riess O
    Arch Neurol; 2003 Sep; 60(9):1266-70. PubMed ID: 12975293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation.
    Bressman SB; de Leon D; Kramer PL; Ozelius LJ; Brin MF; Greene PE; Fahn S; Breakefield XO; Risch NJ
    Ann Neurol; 1994 Nov; 36(5):771-7. PubMed ID: 7979224
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Cortical excitability in DYT-11 positive myoclonus dystonia.
    ; ; Roze E; Apartis E; Trocello JM;
    Mov Disord; 2008 Apr; 23(5):761-4. PubMed ID: 18265016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Early-onset torsion dystonia linked to chromosome 9q34: DYT1].
    Nomura Y
    Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):139-43. PubMed ID: 10434613
    [No Abstract]   [Full Text] [Related]  

  • 18. Opioid binding in DYT1 primary torsion dystonia: an 11C-diprenorphine PET study.
    Whone AL; Von Spiczak S; Edwards M; Valente EM; Hammers A; Bhatia KP; Brooks DJ
    Mov Disord; 2004 Dec; 19(12):1498-503. PubMed ID: 15390064
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microstructural white matter changes in carriers of the DYT1 gene mutation.
    Carbon M; Kingsley PB; Su S; Smith GS; Spetsieris P; Bressman S; Eidelberg D
    Ann Neurol; 2004 Aug; 56(2):283-6. PubMed ID: 15293281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brainstem pathology in DYT1 primary torsion dystonia.
    McNaught KS; Kapustin A; Jackson T; Jengelley TA; Jnobaptiste R; Shashidharan P; Perl DP; Pasik P; Olanow CW
    Ann Neurol; 2004 Oct; 56(4):540-7. PubMed ID: 15455404
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.