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    Results: 1 to 20 of 72

    1.

    SGCE mutations cause psychiatric disorders: clinical and genetic characterization.

    Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR.

    Brain. 2013 Jan;136(Pt 1):294-303. doi: 10.1093/brain/aws308.

    PMID:
    23365103
    [PubMed - indexed for MEDLINE]
    2.

    Metabolic changes in DYT11 myoclonus-dystonia.

    Carbon M, Raymond D, Ozelius L, Saunders-Pullman R, Frucht S, Dhawan V, Bressman S, Eidelberg D.

    Neurology. 2013 Jan 22;80(4):385-91. doi: 10.1212/WNL.0b013e31827f0798. Epub 2013 Jan 2.

    PMID:
    23284065
    [PubMed - indexed for MEDLINE]
    3.

    White matter abnormalities in gene-positive myoclonus-dystonia.

    van der Meer JN, Beukers RJ, van der Salm SM, Caan MW, Tijssen MA, Nederveen AJ.

    Mov Disord. 2012 Nov;27(13):1666-72. doi: 10.1002/mds.25128. Epub 2012 Oct 31.

    PMID:
    23114862
    [PubMed - indexed for MEDLINE]
    4.

    Substance abuse and movement disorders: complex interactions and comorbidities.

    Deik A, Saunders-Pullman R, Luciano MS.

    Curr Drug Abuse Rev. 2012 Sep;5(3):243-53. Review.

    PMID:
    23030352
    [PubMed - indexed for MEDLINE]
    5.

    Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.

    Stamelou M, Mencacci NE, Cordivari C, Batla A, Wood NW, Houlden H, Hardy J, Bhatia KP.

    Neurology. 2012 Jul 31;79(5):435-41. doi: 10.1212/WNL.0b013e318261714a. Epub 2012 Jul 18.

    PMID:
    22815559
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Expression of sarcoglycans in the human cerebral cortex: an immunohistochemical and molecular study.

    Anastasi G, Tomasello F, Di Mauro D, Cutroneo G, Favaloro A, Conti A, Ruggeri A, Rinaldi C, Trimarchi F.

    Cells Tissues Organs. 2012;196(5):470-80. doi: 10.1159/000336842. Epub 2012 Jun 27.

    PMID:
    22738885
    [PubMed - indexed for MEDLINE]
    7.

    Cognition and psychopathology in myoclonus-dystonia.

    van Tricht MJ, Dreissen YE, Cath D, Dijk JM, Contarino MF, van der Salm SM, Foncke EM, Groen JL, Schmand B, Tijssen MA.

    J Neurol Neurosurg Psychiatry. 2012 Aug;83(8):814-20. doi: 10.1136/jnnp-2011-301386. Epub 2012 May 23.

    PMID:
    22626943
    [PubMed - indexed for MEDLINE]
    8.

    The dystrophin-glycoprotein complex in brain development and disease.

    Waite A, Brown SC, Blake DJ.

    Trends Neurosci. 2012 Aug;35(8):487-96. doi: 10.1016/j.tins.2012.04.004. Epub 2012 May 23. Review.

    PMID:
    22626542
    [PubMed - indexed for MEDLINE]
    9.

    Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.

    Dale RC, Grattan-Smith P, Nicholson M, Peters GB.

    Dev Med Child Neurol. 2012 Jul;54(7):618-23. doi: 10.1111/j.1469-8749.2012.04287.x. Epub 2012 Apr 19.

    PMID:
    22515636
    [PubMed - indexed for MEDLINE]
    10.

    Alteration of striatal dopaminergic neurotransmission in a mouse model of DYT11 myoclonus-dystonia.

    Zhang L, Yokoi F, Parsons DS, Standaert DG, Li Y.

    PLoS One. 2012;7(3):e33669. doi: 10.1371/journal.pone.0033669. Epub 2012 Mar 16.

    PMID:
    22438980
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    11.

    Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites.

    Saunders-Pullman R, Raymond D, Stoessl AJ, Hobson D, Nakamura K, Pullman S, Lefton D, Okun MS, Uitti R, Sachdev R, Stanley K, San Luciano M, Hagenah J, Gatti R, Ozelius LJ, Bressman SB.

    Neurology. 2012 Feb 28;78(9):649-57. doi: 10.1212/WNL.0b013e3182494d51. Epub 2012 Feb 15. Erratum in: Neurology. 2012 Mar 27;78(13):1029. Nakamura, T [corrected to Nakamura, K].

    PMID:
    22345219
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    Overview of primary monogenic dystonia.

    Spatola M, Wider C.

    Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S158-61. doi: 10.1016/S1353-8020(11)70049-9. Review.

    PMID:
    22166420
    [PubMed - indexed for MEDLINE]
    13.

    A novel SGCE gene mutation causing myoclonus dystonia in a family with an unusual phenotype.

    Tedroff K, Rolfs A, Norling A.

    Acta Paediatr. 2012 Feb;101(2):e90-2. doi: 10.1111/j.1651-2227.2011.02502.x. Epub 2011 Nov 17.

    PMID:
    22026499
    [PubMed - indexed for MEDLINE]
    14.

    Effect of pallidal deep brain stimulation on psychiatric symptoms in myoclonus-dystonia due to ε-sarcoglycan mutations.

    Contarino MF, Foncke EM, Cath DC, Schuurman PR, Speelman JD, Tijssen MA.

    Arch Neurol. 2011 Aug;68(8):1087-8; author reply 1088-9. doi: 10.1001/archneurol.2011.180. No abstract available.

    PMID:
    21825253
    [PubMed - indexed for MEDLINE]
    15.

    A gain-of-glycosylation mutation associated with myoclonus-dystonia syndrome affects trafficking and processing of mouse ε-sarcoglycan in the late secretory pathway.

    Waite A, De Rosa MC, Brancaccio A, Blake DJ.

    Hum Mutat. 2011 Nov;32(11):1246-58. doi: 10.1002/humu.21561. Epub 2011 Sep 15.

    PMID:
    21796726
    [PubMed - indexed for MEDLINE]
    16.

    Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review.

    Peall KJ, Waite AJ, Blake DJ, Owen MJ, Morris HR.

    Mov Disord. 2011 Aug 15;26(10):1939-42. doi: 10.1002/mds.23791. Epub 2011 Jun 28. Review.

    PMID:
    21713999
    [PubMed - indexed for MEDLINE]
    17.

    A role of diffusion tensor imaging fiber tracking in deep brain stimulation surgery: DBS of the dentato-rubro-thalamic tract (drt) for the treatment of therapy-refractory tremor.

    Coenen VA, Allert N, Mädler B.

    Acta Neurochir (Wien). 2011 Aug;153(8):1579-85; discussion 1585. doi: 10.1007/s00701-011-1036-z. Epub 2011 May 8.

    PMID:
    21553318
    [PubMed - indexed for MEDLINE]
    18.

    Myoclonus-dystonia syndrome.

    Nardocci N.

    Handb Clin Neurol. 2011;100:563-75. doi: 10.1016/B978-0-444-52014-2.00041-0. Review.

    PMID:
    21496608
    [PubMed - indexed for MEDLINE]
    19.

    Nonprimary dystonias.

    Dressler D.

    Handb Clin Neurol. 2011;100:513-38. doi: 10.1016/B978-0-444-52014-2.00038-0. Review.

    PMID:
    21496605
    [PubMed - indexed for MEDLINE]
    20.

    Myoclonus-dystonia in 18p deletion syndrome.

    Kowarik MC, Langer S, Keri C, Hemmer B, Oexle K, Winkelmann J.

    Mov Disord. 2011 Feb 15;26(3):560-1. doi: 10.1002/mds.23446. Epub 2010 Dec 13. No abstract available.

    PMID:
    21462265
    [PubMed - indexed for MEDLINE]

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