BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

632 related articles for article (PubMed ID: 19555827)

  • 1. Genetics and treatment of dystonia.
    Schwarz CS; Bressman SB
    Neurol Clin; 2009 Aug; 27(3):697-718, vi. PubMed ID: 19555827
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetics of dystonia: an overview.
    Bressman SB
    Parkinsonism Relat Disord; 2007; 13 Suppl 3():S347-55. PubMed ID: 18267263
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Monogenetic dystonia: revisiting the dopaminergic hypothesis].
    Blanchard A; Roubertie A; Frédéric MY; Claustres M; Collod-Béroud G
    Rev Neurol (Paris); 2010 Apr; 166(4):389-99. PubMed ID: 19836812
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.
    Groen JL; Ritz K; Contarino MF; van de Warrenburg BP; Aramideh M; Foncke EM; van Hilten JJ; Schuurman PR; Speelman JD; Koelman JH; de Bie RM; Baas F; Tijssen MA
    Mov Disord; 2010 Oct; 25(14):2420-7. PubMed ID: 20687191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetics of dystonia].
    Kamm C
    Fortschr Neurol Psychiatr; 2009 Aug; 77 Suppl 1():S32-6. PubMed ID: 19685389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation screening of the DYT6/THAP1 gene in Italy.
    Bonetti M; Barzaghi C; Brancati F; Ferraris A; Bellacchio E; Giovanetti A; Ialongo T; Zorzi G; Piano C; Petracca M; Albanese A; Nardocci N; Dallapiccola B; Bentivoglio AR; Garavaglia B; Valente EM
    Mov Disord; 2009 Dec; 24(16):2424-7. PubMed ID: 19908325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Early onset torsion dystonia (Oppenheim's dystonia).
    Kamm C
    Orphanet J Rare Dis; 2006 Nov; 1():48. PubMed ID: 17129379
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [New approaches in dystonia (clinical features, genetic issues and pathophysiology].
    Vidailhet M; Grabli D
    Bull Acad Natl Med; 2011; 195(4-5):921-34; discussion 934. PubMed ID: 22375360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and genetic evaluation of DYT1 and DYT6 primary dystonia in China.
    Cheng FB; Wan XH; Feng JC; Wang L; Yang YM; Cui LY
    Eur J Neurol; 2011 Mar; 18(3):497-503. PubMed ID: 20825472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion.
    De Carvalho Aguiar P; Fuchs T; Borges V; Lamar KM; Silva SM; Ferraz HB; Ozelius L
    Mov Disord; 2010 Dec; 25(16):2854-7. PubMed ID: 20925076
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dystonia-causing mutant torsinA inhibits cell adhesion and neurite extension through interference with cytoskeletal dynamics.
    Hewett JW; Zeng J; Niland BP; Bragg DC; Breakefield XO
    Neurobiol Dis; 2006 Apr; 22(1):98-111. PubMed ID: 16361107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.
    Palada V; Stiern S; Glöckle N; Gómez-Garre P; Carrillo F; Mir P; Szczaluba K; Tinazzi M; Ajena D; Romani M; Valente EM; Müller U; Bauer P; Riess O; Ott T; Grundmann K
    Mov Disord; 2012 Jun; 27(7):917. PubMed ID: 22508326
    [No Abstract]   [Full Text] [Related]  

  • 17. No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia.
    Kamm C; Uflacker N; Asmus F; Schrader C; Wolters A; Wittstock M; Pahnke J; Gasser T; Volkmann J; Münchau A; Hagenah J; Benecke R; Klein C; Lohmann K
    Mov Disord; 2011 Sep; 26(11):2136-7. PubMed ID: 21638323
    [No Abstract]   [Full Text] [Related]  

  • 18. Dystonia: genetics and treatment update.
    Bhidayasiri R
    Neurologist; 2006 Mar; 12(2):74-85. PubMed ID: 16534444
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6).
    Kaiser FJ; Osmanoric A; Rakovic A; Erogullari A; Uflacker N; Braunholz D; Lohnau T; Orolicki S; Albrecht M; Gillessen-Kaesbach G; Klein C; Lohmann K
    Ann Neurol; 2010 Oct; 68(4):554-9. PubMed ID: 20976771
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.