157 related articles for article (PubMed ID: 17017572)
1. Genetics of dystonia.
Bressman S
J Neural Transm Suppl; 2006; (70):489-95. PubMed ID: 17017572
[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. Increased risk for recurrent major depression in DYT1 dystonia mutation carriers.
Heiman GA; Ottman R; Saunders-Pullman RJ; Ozelius LJ; Risch NJ; Bressman SB
Neurology; 2004 Aug; 63(4):631-7. PubMed ID: 15326234
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Non-DYT1 early-onset primary torsion dystonia: comparison with DYT1 phenotype and review of the literature.
Fasano A; Nardocci N; Elia AE; Zorzi G; Bentivoglio AR; Albanese A
Mov Disord; 2006 Sep; 21(9):1411-8. PubMed ID: 16773641
[TBL] [Abstract][Full Text] [Related]
8. DYT1 mutation in primary torsion dystonia in a Serbian population.
Major T; Svetel M; Romac S; Kostić VS
J Neurol; 2001 Nov; 248(11):940-3. PubMed ID: 11757956
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic variability of the DYT1 mutation in German dystonia patients.
Leube B; Kessler KR; Ferbert A; Ebke M; Schwendemann G; Erbguth F; Benecke R; Auburger G
Acta Neurol Scand; 1999 Apr; 99(4):248-51. PubMed ID: 10225357
[TBL] [Abstract][Full Text] [Related]
10. Frequency of the DYT1 mutation in primary torsion dystonia without family history.
Brassat D; Camuzat A; Vidailhet M; Feki I; Jedynak P; Klap P; Agid Y; Dürr A; Brice A
Arch Neurol; 2000 Mar; 57(3):333-5. PubMed ID: 10714658
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Primary torsion dystonia due to the Tor1A GAG deletion in an Irish family.
O'Riordan S; Cockburn D; Barton D; Lynch T; Hutchinson M
Ir J Med Sci; 2002; 171(1):31-2. PubMed ID: 11993591
[TBL] [Abstract][Full Text] [Related]
13. Search for a founder mutation in idiopathic focal dystonia from Northern Germany.
Klein C; Ozelius LJ; Hagenah J; Breakefield XO; Risch NJ; Vieregge P
Am J Hum Genet; 1998 Dec; 63(6):1777-82. PubMed ID: 9837831
[TBL] [Abstract][Full Text] [Related]
14. Late onset rest-tremor in DYT1 dystonia.
Stamelou M; Edwards MJ; Bhatia KP
Parkinsonism Relat Disord; 2013 Jan; 19(1):136-7. PubMed ID: 22721973
[No Abstract] [Full Text] [Related]
15. De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.
Klein C; Brin MF; de Leon D; Limborska SA; Ivanova-Smolenskaya IA; Bressman SB; Friedman A; Markova ED; Risch NJ; Breakefield XO; Ozelius LJ
Hum Mol Genet; 1998 Jul; 7(7):1133-6. PubMed ID: 9618171
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. The DYT1 phenotype and guidelines for diagnostic testing.
Bressman SB; Sabatti C; Raymond D; de Leon D; Klein C; Kramer PL; Brin MF; Fahn S; Breakefield X; Ozelius LJ; Risch NJ
Neurology; 2000 May; 54(9):1746-52. PubMed ID: 10802779
[TBL] [Abstract][Full Text] [Related]
18. Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia.
Risch NJ; Bressman SB; Senthil G; Ozelius LJ
Am J Hum Genet; 2007 Jun; 80(6):1188-93. PubMed ID: 17503336
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. DYT1 mutation in Japanese patients with primary torsion dystonia.
Matsumoto S; Nishimura M; Kaji R; Sakamoto T; Mezaki T; Shimazu H; Murase N; Shibasaki H
Neuroreport; 2001 Mar; 12(4):793-5. PubMed ID: 11277585
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
