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There are 7828918 results for: content related to: Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene

  1. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

  2. Milestones in dystonia

    Movement Disorders

    Volume 26, Issue 6, May 2011, Pages: 1106–1126, Laurie J. Ozelius, Naomi Lubarr and Susan B. Bressman

    Version of Record online : 27 MAY 2011, DOI: 10.1002/mds.23775

  3. Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia

    Movement Disorders

    Volume 17, Issue 2, March/April 2002, Pages: 392–397, Francesco Brancati, Giovanni Defazio, Viviana Caputo, Enza Maria Valente, Antonio Pizzuti, Paolo Livrea, Alfredo Berardelli and Bruno Dallapiccola

    Version of Record online : 12 FEB 2002, DOI: 10.1002/mds.10077

  4. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Version of Record online : 6 JUN 2014, DOI: 10.1002/mds.25914

  5. Non-DYT1 early-onset primary torsion dystonia: Comparison with DYT1 phenotype and review of the literature

    Movement Disorders

    Volume 21, Issue 9, September 2006, Pages: 1411–1418, Alfonso Fasano, Nardo Nardocci, Antonio Emanuele Elia, Giovanna Zorzi, Anna Rita Bentivoglio and Alberto Albanese

    Version of Record online : 13 JUN 2006, DOI: 10.1002/mds.21000

  6. Poster session 1, Abstracts 177–312

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S76–S116,

    Version of Record online : 10 MAY 2004, DOI: 10.1002/mds.20172

  7. Phenotypic variability of DYT1-PTD: Does the clinical spectrum include psychogenic dystonia?

    Movement Disorders

    Volume 17, Issue 5, September/October 2002, Pages: 1058–1063, Anna Rita Bentivoglio, Mario Loi, Enza M. Valente, Tamara Ialongo, Pietro Tonali and Alberto Albanese

    Version of Record online : 25 APR 2002, DOI: 10.1002/mds.10236

  8. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  9. Abstracts of The Movement Disorder Society's Twelfth International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 23, Issue S1, 15 May 2008, Pages: S1–S422,

    Version of Record online : 28 MAY 2008, DOI: 10.1002/mds.22133

  10. Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish–Mennonites

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 18, 15 September 2007, Pages: 2098–2105, Rachel Saunders-Pullman, Deborah Raymond, Geetha Senthil, Patricia Kramer, Erin Ohmann, Amanda Deligtisch, Vicki Shanker, Paul Greene, Rowena Tabamo, Neng Huang, Michele Tagliati, Patricia Kavanagh, Jeannie Soto-Valencia, Patricia de Carvalho Aguiar, Neil Risch, Laurie Ozelius and Susan Bressman

    Version of Record online : 13 AUG 2007, DOI: 10.1002/ajmg.a.31887

  11. Phenotypic characterization of DYT13 primary torsion dystonia

    Movement Disorders

    Volume 19, Issue 2, February 2004, Pages: 200–206, Anna Rita Bentivoglio, Tamara Ialongo, M. Fiorella Contarino, Enza M. Valente and Alberto Albanese

    Version of Record online : 10 OCT 2003, DOI: 10.1002/mds.10634

  12. Onset and progression of primary torsion dystonia in sporadic and familial cases

    European Journal of Neurology

    Volume 13, Issue 10, October 2006, Pages: 1083–1088, A. E. Elia, G. Filippini, A. R. Bentivoglio, A. Fasano, T. Ialongo and A. Albanese

    Version of Record online : 20 SEP 2006, DOI: 10.1111/j.1468-1331.2006.01387.x

  13. Atypical phenotypes and clinical variability in a large Italian family with DYT1–primary torsion dystonia

    Movement Disorders

    Volume 21, Issue 10, October 2006, Pages: 1782–1784, Mattia Gambarin, Enza Maria Valente, Paolo Liberini, Giuseppe Barrano, Alberto Bonizzato, Alessandro Padovani, Giuseppe Moretto, Mirta Fiorio, Bruno Dallapiccola, Nicola Smania, Antonio Fiaschi and Michele Tinazzi

    Version of Record online : 27 JUL 2006, DOI: 10.1002/mds.21056

  14. Review: Genetics and neuropathology of primary pure dystonia

    Neuropathology and Applied Neurobiology

    Volume 38, Issue 6, October 2012, Pages: 520–534, R. Paudel, J. Hardy, T. Revesz, J. L. Holton and H. Houlden

    Version of Record online : 17 SEP 2012, DOI: 10.1111/j.1365-2990.2012.01298.x

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    Abstracts of The Movement Disorder Society's Eleventh International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 22, Issue S16, 2007, Pages: S1–S325,

    Version of Record online : 24 APR 2007, DOI: 10.1002/mds.21535

  16. DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13–36.32 in an Italian family with cranial-cervical or upper limb onset

    Annals of Neurology

    Volume 49, Issue 3, 1 March 2001, Pages: 362–366, Enza Maria Valente, Anna Rita Bentivoglio, Emanuele Cassetta, Peter H. Dixon, Mary B. Davis, Alessandro Ferraris, Tamara Ialongo, Marina Frontali, Nicholas W. Wood and Alberto Albanese

    Version of Record online : 1 MAR 2001, DOI: 10.1002/ana.73

  17. Microstructural white matter changes in primary torsion dystonia

    Movement Disorders

    Volume 23, Issue 2, 30 January 2008, Pages: 234–239, Maren Carbon, Peter B. Kingsley, Chengke Tang, Susan Bressman and David Eidelberg

    Version of Record online : 12 NOV 2007, DOI: 10.1002/mds.21806

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    Poster Session

    Movement Disorders

    Volume 31, Issue S2, June 2016, Pages: S1–S697,

    Version of Record online : 19 JUN 2016, DOI: 10.1002/mds.26688

  19. Opioid binding in DYT1 primary torsion dystonia: An 11C-diprenorphine PET study

    Movement Disorders

    Volume 19, Issue 12, December 2004, Pages: 1498–1503, Alan L. Whone, Sarah Von Spiczak, Mark Edwards, Enza-Maria Valente, Alexander Hammers, Kailash P. Bhatia and David J. Brooks

    Version of Record online : 15 JUL 2004, DOI: 10.1002/mds.20238

  20. Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias

    Movement Disorders

    Volume 19, Issue 11, November 2004, Pages: 1294–1297, Kathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, Juliane Vollmer-Haase, Peter Bauer, Manfred Stuhrmann, Thorsten Schulte, Ludger Schöls, Helge Topka and Olaf Riess

    Version of Record online : 26 MAY 2004, DOI: 10.1002/mds.20128