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There are 18081 results for: content related to: Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families

  1. Milestones in dystonia

    Movement Disorders

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

    Article first published online : 27 MAY 2011, DOI: 10.1002/mds.23775

  2. Exclusion of the DYT1 locus in familial torticollis

    Annals of Neurology

    Volume 40, Issue 4, October 1996, Pages: 681–684, Dr S. B. Bressman, P. E. Greene, D. Raymond, B. Ford, D. de Leon, S. Fahn, T. G. Nygaard, T. T. Warner, L. Almasy, R. J. Uitti, G. A. Heiman, P. L. Kramer, N. J. Risch, D. M. Maraganore and A. E. Harding

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410400421

  3. Primary Dystonias

    Hyperkinetic Movement Disorders: Differential Diagnosis and Treatment

    Antonio E. Elia, Alberto Albanese, Pages: 113–134, 2012

    Published Online : 24 FEB 2012, DOI: 10.1002/9781444346183.ch8

  4. Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation

    Annals of Neurology

    Volume 36, Issue 5, November 1994, Pages: 771–777, Dr Susan B. Bressman, Deborah de Leon, Patricia L. Kramer, Laurie J. Ozelius, Mitchell F. Brin, Paul E. Greene, Stanley Fahn, Xandra O. Breakefield and Neil J. Risch

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410360514

  5. Italian family with cranial cervical dystonia: Clinical and genetic study

    Movement Disorders

    Volume 14, Issue 5, September 1999, Pages: 820–825, Emanuele Cassetta, Nicoletta Del Grosso, Anna Rita Bentivoglio, Enza Maria Valente, Marina Frontali and Alberto Albanese

    Article first published online : 16 JAN 2001, DOI: 10.1002/1531-8257(199909)14:5<820::AID-MDS1015>3.0.CO;2-I

  6. A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia

    Movement Disorders

    Volume 15, Issue 5, September 2000, Pages: 954–959, A. Münchau, E. M. Valente, M. B. Davis, V. Stinton, N. W. Wood, N. P. Quinn and Kailash P. Bhatia

    Article first published online : 23 JAN 2001, DOI: 10.1002/1531-8257(200009)15:5<954::AID-MDS1028>3.0.CO;2-I

  7. 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

    Article first published online : 10 OCT 2003, DOI: 10.1002/mds.10634

  8. Ethnic variation in the clinical expression of idiopathic torsion dystonia

    Movement Disorders

    Volume 12, Issue 5, September 1997, Pages: 715–721, Dr. Laura Almasy, Susan Bressman, Deborah de Leon and Neil Risch

    Article first published online : 4 NOV 2004, DOI: 10.1002/mds.870120515

  9. 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

    Article first published online : 17 SEP 2012, DOI: 10.1111/j.1365-2990.2012.01298.x

  10. 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

    Article first published online : 1 MAR 2001, DOI: 10.1002/ana.73

  11. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia

    Movement Disorders

    Volume 9, Issue 6, 1994, Pages: 626–632, Dr. Susan B. Bressman, Dr. Ann L. Hunt, Gary A. Heiman, Mitchell F. Brin, Robert E. Burke, Stanley Fahn, Joel M. Trugman, Deborah de Leon, Patricia L. Kramer, Kirk C. Wilhelmsen and Torbjoern G. Nygaard

    Article first published online : 12 OCT 2004, DOI: 10.1002/mds.870090608

  12. The Autosomal Dominant Dystonias

    Brain Pathology

    Volume 2, Issue 4, October 1992, Pages: 297–308, Thomas Gasser, Stanley Fahn and Xandra O. Breakefield

    Article first published online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1992.tb00707.x

  13. 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

    Article first published online : 13 AUG 2007, DOI: 10.1002/ajmg.a.31887

  14. 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

    Article first published online : 12 FEB 2002, DOI: 10.1002/mds.10077

  15. You have free access to this content
    A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia

    Human Mutation

    Volume 14, Issue 3, 1999, Page: 269, Petr A. Slominsky, Elena D. Markova, Marya I. Shadrina, Sergey N. Illarioshkin, Natalia I. Miklina, Svetlana A. Limborska and Irina A. Ivanova-Smolenskaya

    Article first published online : 2 SEP 1999, DOI: 10.1002/(SICI)1098-1004(1999)14:3<269::AID-HUMU12>3.0.CO;2-9

  16. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from south tyrol

    Annals of Neurology

    Volume 44, Issue 3, September 1998, Pages: 394–398, Christine Klein, Peter P. Pramstaller, Claudio C. Castellan, Xandra O. Breakefield, Patricia L. Kramer and Dr. Laurie J. Ozelius

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410440318

  17. 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

    Article first published online : 20 SEP 2006, DOI: 10.1111/j.1468-1331.2006.01387.x

  18. Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families

    Clinical Genetics

    Volume 64, Issue 2, August 2003, Pages: 153–159, J Carmona, JA Burguera, B Mollà, F Mulas, P Smeyers, F Carratalà, JG De Yebenes, J Hoenicka and F Palau

    Article first published online : 10 JUL 2003, DOI: 10.1034/j.1399-0004.2003.00084.x

  19. Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe

    American Journal of Medical Genetics

    Volume 74, Issue 5, 19 September 1997, Pages: 529–532, B. Leube, T. Hendgen, K.R. Kessler, M. Knapp, R. Benecke and G. Auburger

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970919)74:5<529::AID-AJMG15>3.0.CO;2-E

  20. Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset

    Annals of Neurology

    Volume 44, Issue 1, July 1998, Pages: 126–128, Dr. T. Gasser, K. Windgassen, B. Bereznai, C. Kabus and A. C. Ludolph

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410440119