154 related articles for article (PubMed ID: 18571468)
1. Impaired body movement representation in DYT1 mutation carriers.
Fiorio M; Gambarin M; Defazio G; Valente EM; Stanzani C; Moretto G; Loi M; Soliveri P; Nardocci N; Albanese A; Fiaschi A; Tinazzi M
Clin Neurophysiol; 2008 Aug; 119(8):1864-1869. PubMed ID: 18571468
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Impaired sequence learning in dystonia mutation carriers: a genotypic effect.
Carbon M; Argyelan M; Ghilardi MF; Mattis P; Dhawan V; Bressman S; Eidelberg D
Brain; 2011 May; 134(Pt 5):1416-27. PubMed ID: 21515903
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Increased sensorimotor network activity in DYT1 dystonia: a functional imaging study.
Carbon M; Argyelan M; Habeck C; Ghilardi MF; Fitzpatrick T; Dhawan V; Pourfar M; Bressman SB; Eidelberg D
Brain; 2010 Mar; 133(Pt 3):690-700. PubMed ID: 20207699
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. 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]
9. Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystonia.
Szczaluba K; Jurek M; Milewski M; Friedman A; Kadziolka B; Szolna A; Bal J; Mazurczak T
Eur J Neurol; 2007 Jun; 14(6):659-62. PubMed ID: 17539945
[TBL] [Abstract][Full Text] [Related]
10. Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia.
Dang MT; Yokoi F; McNaught KS; Jengelley TA; Jackson T; Li J; Li Y
Exp Neurol; 2005 Dec; 196(2):452-63. PubMed ID: 16242683
[TBL] [Abstract][Full Text] [Related]
11. Impaired sequence learning in carriers of the DYT1 dystonia mutation.
Ghilardi MF; Carbon M; Silvestri G; Dhawan V; Tagliati M; Bressman S; Ghez C; Eidelberg D
Ann Neurol; 2003 Jul; 54(1):102-9. PubMed ID: 12838525
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Phenotype of the DYT1 mutation in the TOR1A gene in a Polish population of patients with dystonia. A preliminary report.
Gajos A; Piaskowski S; Sławek J; Ochudło S; Opala G; Łobińska A; Honczarenko K; Budrewicz S; Koszewicz M; Pełszyńska B; Liberski PP; Bogucki A
Neurol Neurochir Pol; 2007; 41(6):487-94. PubMed ID: 18224570
[TBL] [Abstract][Full Text] [Related]
14. DYT1 mutations amongst early onset primary dystonia patients in China.
Yang JF; Li JY; Li YJ; Wu T; Zhang YL; Chen B
Chin Med Sci J; 2008 Mar; 23(1):38-43. PubMed ID: 18437909
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Impact of bilateral pallidal stimulation on DYT1-generalized dystonia in Japanese patients.
Goto S; Yamada K; Shimazu H; Murase N; Matsuzaki K; Tamura T; Nagahiro S; Kuratsu J; Kaji R
Mov Disord; 2006 Oct; 21(10):1785-7. PubMed ID: 16830314
[TBL] [Abstract][Full Text] [Related]
17. Genotype-phenotype interactions in primary dystonias revealed by differential changes in brain structure.
Draganski B; Schneider SA; Fiorio M; Klöppel S; Gambarin M; Tinazzi M; Ashburner J; Bhatia KP; Frackowiak RS
Neuroimage; 2009 Oct; 47(4):1141-7. PubMed ID: 19344776
[TBL] [Abstract][Full Text] [Related]
18. The role of DYT1 in primary torsion dystonia in Europe.
Valente EM; Warner TT; Jarman PR; Mathen D; Fletcher NA; Marsden CD; Bhatia KP; Wood NW
Brain; 1998 Dec; 121 ( Pt 12)():2335-9. PubMed ID: 9874484
[TBL] [Abstract][Full Text] [Related]
19. Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study.
Martino D; Gajos A; Gallo V; Cif L; Coubes P; Tinazzi M; Schneider SA; Fiorio M; Zorzi G; Nardocci N; Ben-Shlomo Y; Edwards MJ; Bhatia KP
J Neurol; 2013 Apr; 260(4):1081-6. PubMed ID: 23212755
[TBL] [Abstract][Full Text] [Related]
20. Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.
Akbari MT; Zand Z; Shahidi GA; Hamid M
Med Princ Pract; 2012; 21(5):462-6. PubMed ID: 22487959
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]