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 *

128 related articles for article (PubMed ID: 12614318)

  • 1. Focal and segmental primary dystonia in north-western Germany--a clinico-genetic study.
    Maniak S; Sieberer M; Hagenah J; Klein C; Vieregge P
    Acta Neurol Scand; 2003 Mar; 107(3):228-32. PubMed ID: 12614318
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. Clinical and genetic evaluation in a French population presenting with primary focal dystonia.
    Dhaenens CM; Krystkowiak P; Douay X; Charpentier P; Bele S; Destée A; Sablonnière B
    Mov Disord; 2005 Jul; 20(7):822-5. PubMed ID: 15726581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Writer's cramp in an Australian pedigree with DYT1 dystonia.
    van den Bos M; Marotta R; Goldup S; Chataway T; Firgaira F; Thyagarajan D
    J Clin Neurosci; 2004 Jun; 11(5):537-9. PubMed ID: 15177405
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Three brothers with a very-late-onset writer's cramp.
    Bhidayasiri R; Jen JC; Baloh RW
    Mov Disord; 2005 Oct; 20(10):1375-7. PubMed ID: 15954129
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Age at onset as a factor in determining the phenotype of primary torsion dystonia.
    O'Riordan S; Raymond D; Lynch T; Saunders-Pullman R; Bressman SB; Daly L; Hutchinson M
    Neurology; 2004 Oct; 63(8):1423-6. PubMed ID: 15505159
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A genetic study of idiopathic focal dystonias.
    Waddy HM; Fletcher NA; Harding AE; Marsden CD
    Ann Neurol; 1991 Mar; 29(3):320-4. PubMed ID: 2042948
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genetic study of idiopathic focal dystonias.
    Stojanović M; Cvetković D; Kostić VS
    J Neurol; 1995 Aug; 242(8):508-11. PubMed ID: 8530978
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sex Differences in Dystonia.
    Kilic-Berkmen G; Scorr LM; McKay L; Thayani M; Donsante Y; Perlmutter JS; Norris SA; Wright L; Klein C; Feuerstein JS; Mahajan A; Wagle-Shukla A; Malaty I; LeDoux MS; Pirio-Richardson S; Pantelyat A; Moukheiber E; Frank S; Ondo W; Saunders-Pullman R; Lohmann K; Hess EJ; Jinnah HA
    Mov Disord Clin Pract; 2024 Aug; 11(8):973-982. PubMed ID: 38778444
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Intrafamilial phenotypic and genetic heterogeneity of dystonia.
    Kostić VS; Svetel M; Kabakci K; Ristić A; Petrović I; Schüle B; Kock N; Djarmati A; Romac S; Klein C
    J Neurol Sci; 2006 Dec; 250(1-2):92-6. PubMed ID: 17027035
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotypes and genetic architecture of focal primary torsion dystonia.
    Groen JL; Kallen MC; van de Warrenburg BP; Speelman JD; van Hilten JJ; Aramideh M; Boon AJ; Klein C; Koelman JH; Langeveld TP; Baas F; Tijssen MA
    J Neurol Neurosurg Psychiatry; 2012 Oct; 83(10):1006-11. PubMed ID: 22773857
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.