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 *

195 related articles for article (PubMed ID: 9874484)

  • 1. 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]  

  • 2. Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspects.
    Klein C; Friedman J; Bressman S; Vieregge P; Brin MF; Pramstaller PP; De Leon D; Hagenah J; Sieberer M; Fleet C; Kiely R; Xin W; Breakefield XO; Ozelius LJ; Sims KB
    Genet Test; 1999; 3(4):323-8. PubMed ID: 10627938
    [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. DYT1 mutation in French families with idiopathic torsion dystonia.
    Lebre AS; Durr A; Jedynak P; Ponsot G; Vidailhet M; Agid Y; Brice A
    Brain; 1999 Jan; 122 ( Pt 1)():41-5. PubMed ID: 10050893
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Phenotypic variability of DYT1-PTD: does the clinical spectrum include psychogenic dystonia?
    Bentivoglio AR; Loi M; Valente EM; Ialongo T; Tonali P; Albanese A
    Mov Disord; 2002 Sep; 17(5):1058-63. PubMed ID: 12360559
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
    Kamm C; Castelon-Konkiewitz E; Naumann M; Heinen F; Brack M; Nebe A; Ceballos-Baumann A; Gasser T
    Mov Disord; 1999 Jul; 14(4):681-3. PubMed ID: 10435508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 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. Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
    Valente EM; Povey S; Warner TT; Wood NW; Davis MB
    Ann Hum Genet; 1999 Jan; 63(Pt 1):1-8. PubMed ID: 10738516
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic storm.
    Opal P; Tintner R; Jankovic J; Leung J; Breakefield XO; Friedman J; Ozelius L
    Mov Disord; 2002 Mar; 17(2):339-45. PubMed ID: 11921121
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.