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Journal Abstract Search

417 related items for PubMed ID: 19441135

  • 1. 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 15; 24(9):1390-2. PubMed ID: 19441135
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  • 2. 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 15; 60(9):1266-70. PubMed ID: 12975293
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  • 3. 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 15; 11(5):537-9. PubMed ID: 15177405
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  • 4. Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp.
    Koukouni V, Valente EM, Cordivari C, Bhatia KP, Quinn NP.
    Mov Disord; 2008 Oct 15; 23(13):1913-5. PubMed ID: 18702114
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  • 7. 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 01; 250(1-2):92-6. PubMed ID: 17027035
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  • 10. Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset.
    Gasser T, Windgassen K, Bereznai B, Kabus C, Ludolph AC.
    Ann Neurol; 1998 Jul 01; 44(1):126-8. PubMed ID: 9667600
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  • 11. 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 01; 15(6):1238-41. PubMed ID: 11104212
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  • 12. [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 04; 87(33):2324-7. PubMed ID: 18036294
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  • 13. Early onset primary dystonia.
    Zorzi G, Zibordi F, Garavaglia B, Nardocci N.
    Eur J Paediatr Neurol; 2009 Nov 04; 13(6):488-92. PubMed ID: 19157930
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  • 19. Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.
    Kamm C, Asmus F, Mueller J, Mayer P, Sharma M, Muller UJ, Beckert S, Ehling R, Illig T, Wichmann HE, Poewe W, Mueller JC, Gasser T.
    Neurology; 2006 Nov 28; 67(10):1857-9. PubMed ID: 17130424
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