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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

267 related items for PubMed ID: 9667600

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  • 2. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.
    Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ.
    Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609
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  • 3. 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
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  • 4. Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.
    Gasser T, Bove CM, Ozelius LJ, Hallett M, Charness ME, Hochberg FH, Breakefield XO.
    Mov Disord; 1996 Mar; 11(2):163-6. PubMed ID: 8684386
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  • 6. 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
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  • 7. 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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  • 8. 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 15; 21(10):1782-4. PubMed ID: 16874761
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  • 11. A single family with writer's cramp, essential tremor, and primary writing tremor.
    Cohen LG, Hallett M, Sudarsky L.
    Mov Disord; 1987 Oct 15; 2(2):109-16. PubMed ID: 3504263
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  • 14. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.
    Bressman SB, Hunt AL, Heiman GA, Brin MF, Burke RE, Fahn S, Trugman JM, de Leon D, Kramer PL, Wilhelmsen KC.
    Mov Disord; 1994 Nov 15; 9(6):626-32. PubMed ID: 7845403
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  • 17. 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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  • 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 Dec 01; 41(6):487-94. PubMed ID: 18224570
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