These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 16631205)

  • 1. DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West.
    Jamora RD; Tan EK; Liu CP; Kathirvel P; Burgunder JM; Tan LC
    J Neurol Sci; 2006 Aug; 247(1):35-7. PubMed ID: 16631205
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Mutations in DYT1: extension of the phenotypic and mutational spectrum.
    Kabakci K; Hedrich K; Leung JC; Mitterer M; Vieregge P; Lencer R; Hagenah J; Garrels J; Witt K; Klostermann F; Svetel M; Friedman J; Kostic V; Bressman SB; Breakefield XO; Ozelius LJ; Pramstaller PP; Klein C
    Neurology; 2004 Feb; 62(3):395-400. PubMed ID: 14872019
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Identification of DYT1 mutation in patients with primary torsion dystonia patients in China].
    Yang JF; Li JY; Li YJ; Zhang YL; Chen B
    Zhonghua Yi Xue Za Zhi; 2007 Sep; 87(33):2324-7. PubMed ID: 18036294
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China.
    Zhang SS; Fang DF; Hu XH; Burgunder JM; Chen XP; Zhang YW; Shang HF
    Eur J Neurol; 2010 Jun; 17(6):846-51. PubMed ID: 20113340
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DYT1 mutations in early onset primary torsion dystonia and Parkinson disease patients in Chinese populations.
    Yang JF; Wu T; Li JY; Li YJ; Zhang YL; Chan P
    Neurosci Lett; 2009 Jan; 450(2):117-21. PubMed ID: 19038309
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-throughput mutational analysis of TOR1A in primary dystonia.
    Xiao J; Bastian RW; Perlmutter JS; Racette BA; Tabbal SD; Karimi M; Paniello RC; Blitzer A; Batish SD; Wszolek ZK; Uitti RJ; Hedera P; Simon DK; Tarsy D; Truong DD; Frei KP; Pfeiffer RF; Gong S; Zhao Y; LeDoux MS
    BMC Med Genet; 2009 Mar; 10():24. PubMed ID: 19284587
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Clinical characterization and evaluation of DYT1 gene in Indian primary dystonia patients.
    Naiya T; Biswas A; Neogi R; Datta S; Misra AK; Das SK; Ray K; Ray J
    Acta Neurol Scand; 2006 Sep; 114(3):210-5. PubMed ID: 16911351
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The DYT1 GAG deletion is infrequent in sporadic and familial writer' s cramp.
    Kamm C; Naumann M; Mueller J; Mai N; Riedel L; Wissel J; Gasser T
    Mov Disord; 2000 Nov; 15(6):1238-41. PubMed ID: 11104212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mouse model of rare TOR1A variant found in sporadic focal dystonia impairs domains affected in DYT1 dystonia patients and animal models.
    Bhagat SL; Qiu S; Caffall ZF; Wan Y; Pan Y; Rodriguiz RM; Wetsel WC; Badea A; Hochgeschwender U; Calakos N
    Neurobiol Dis; 2016 Sep; 93():137-45. PubMed ID: 27168150
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Investigating DYT1 in a Taiwanese dystonia cohort.
    Wu MC; Chang YY; Chen YF; Lan MY; Chen PL; Tai CH; Lin CH
    J Formos Med Assoc; 2022 Jan; 121(1 Pt 2):375-380. PubMed ID: 34092466
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [DYT1 positive generalised dystonia: a case study of two siblings].
    Bereznai B; Baraczka K; Nagy Z; Molnár MJ
    Ideggyogy Sz; 2007 Jul; 60(7-8):342-7. PubMed ID: 17713116
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency of DYT1 mutation in early onset primary dystonia in Italian patients.
    Zorzi G; Garavaglia B; Invernizzi F; Girotti F; Soliveri P; Zeviani M; Angelini L; Nardocci N
    Mov Disord; 2002 Mar; 17(2):407-8. PubMed ID: 11921134
    [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. Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp.
    Ritz K; Groen JL; Kruisdijk JJ; Baas F; Koelman JH; Tijssen MA
    Mov Disord; 2009 Jul; 24(9):1390-2. PubMed ID: 19441135
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited.
    Dobričić V; Kresojević N; Žarković M; Tomić A; Marjanović A; Westenberger A; Cvetković D; Svetel M; Novaković I; Kostić VS
    Parkinsonism Relat Disord; 2015 Oct; 21(10):1256-9. PubMed ID: 26297380
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.