230 related articles for article (PubMed ID: 17947338)
1. Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study.
Carbon M; Ghilardi MF; Argyelan M; Dhawan V; Bressman SB; Eidelberg D
Brain; 2008 Jan; 131(Pt 1):146-54. PubMed ID: 17947338
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Functional imaging in hereditary dystonia.
Carbon M; Argyelan M; Eidelberg D
Eur J Neurol; 2010 Jul; 17 Suppl 1(0 1):58-64. PubMed ID: 20590810
[TBL] [Abstract][Full Text] [Related]
7. Abnormal structure-function relationships in hereditary dystonia.
Carbon M; Eidelberg D
Neuroscience; 2009 Nov; 164(1):220-9. PubMed ID: 19162138
[TBL] [Abstract][Full Text] [Related]
8. Functional imaging of sequence learning in Parkinson's disease.
Carbon M; Eidelberg D
J Neurol Sci; 2006 Oct; 248(1-2):72-7. PubMed ID: 16753182
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A functional MRI study of motor dysfunction in Friedreich's ataxia.
Akhlaghi H; Corben L; Georgiou-Karistianis N; Bradshaw J; Delatycki MB; Storey E; Egan GF
Brain Res; 2012 Aug; 1471():138-54. PubMed ID: 22771856
[TBL] [Abstract][Full Text] [Related]
11. Neuroimaging findings in DYT1 dystonia and the pathophysiological implication: A systematic review.
Taiwo FT; Adebayo PB
Brain Behav; 2023 Jun; 13(6):e3023. PubMed ID: 37165749
[TBL] [Abstract][Full Text] [Related]
12. Disorganized sensorimotor integration in mutation-positive myoclonus-dystonia: a functional magnetic resonance imaging study.
Beukers RJ; Foncke EM; van der Meer JN; Nederveen AJ; de Ruiter MB; Bour LJ; Veltman DJ; Tijssen MA
Arch Neurol; 2010 Apr; 67(4):469-74. PubMed ID: 20385914
[TBL] [Abstract][Full Text] [Related]
13. Caudate nucleus: influence of dopaminergic input on sequence learning and brain activation in Parkinsonism.
Carbon M; Ma Y; Barnes A; Dhawan V; Chaly T; Ghilardi MF; Eidelberg D
Neuroimage; 2004 Apr; 21(4):1497-507. PubMed ID: 15050574
[TBL] [Abstract][Full Text] [Related]
14. In vivo evidence for GABA(A) receptor changes in the sensorimotor system in primary dystonia.
Garibotto V; Romito LM; Elia AE; Soliveri P; Panzacchi A; Carpinelli A; Tinazzi M; Albanese A; Perani D
Mov Disord; 2011 Apr; 26(5):852-7. PubMed ID: 21370265
[TBL] [Abstract][Full Text] [Related]
15. Hypertrophy of nigral neurons in Torsin1A deletion (DYT1) carriers manifesting dystonia.
Iacono D; Geraci-Erck M; Peng H; Rabin ML; Kurlan R
Parkinsonism Relat Disord; 2019 Jan; 58():63-69. PubMed ID: 30193818
[TBL] [Abstract][Full Text] [Related]
16. Functional networks in motor sequence learning: abnormal topographies in Parkinson's disease.
Nakamura T; Ghilardi MF; Mentis M; Dhawan V; Fukuda M; Hacking A; Moeller JR; Ghez C; Eidelberg D
Hum Brain Mapp; 2001 Jan; 12(1):42-60. PubMed ID: 11198104
[TBL] [Abstract][Full Text] [Related]
17. Metabolic changes in DYT11 myoclonus-dystonia.
Carbon M; Raymond D; Ozelius L; Saunders-Pullman R; Frucht S; Dhawan V; Bressman S; Eidelberg D
Neurology; 2013 Jan; 80(4):385-91. PubMed ID: 23284065
[TBL] [Abstract][Full Text] [Related]
18. Beneficial effects of cerebellar tDCS on motor learning are associated with altered putamen-cerebellar connectivity: A simultaneous tDCS-fMRI study.
Liebrand M; Karabanov A; Antonenko D; Flöel A; Siebner HR; Classen J; Krämer UM; Tzvi E
Neuroimage; 2020 Dec; 223():117363. PubMed ID: 32919057
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Longitudinal Changes in the Motor Learning-Related Brain Activation Response in Presymptomatic Huntington's Disease.
Holtbernd F; Tang CC; Feigin A; Dhawan V; Ghilardi MF; Paulsen JS; Guttman M; Eidelberg D
PLoS One; 2016; 11(5):e0154742. PubMed ID: 27192167
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
