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There are 112873 results for: content related to: The contribution of a spinal mechanism in developing peripheral myoclonus: A case report

  1. Clinical analysis in familial cortical myoclonic tremor allows differential diagnosis with essential tremor

    Movement Disorders

    Volume 21, Issue 5, May 2006, Pages: 599–608, Frédéric Bourdain, Emmanuelle Apartis, Jean-Marc Trocello, Jean-Sébastien Vidal, Pascal Masnou, Laurent Vercueil and Marie Vidailhet

    Article first published online : 9 NOV 2005, DOI: 10.1002/mds.20725

  2. Clinical and neurophysiological characterization of myoclonus in complex regional pain syndrome

    Movement Disorders

    Volume 23, Issue 4, 15 March 2008, Pages: 581–587, Alexander G. Munts, Anne-Fleur Van Rootselaar, Johan N. Van Der Meer, Johannes H.T.M. Koelman, Jacobus J. Van Hilten and Marina A.J. Tijssen

    Article first published online : 28 DEC 2007, DOI: 10.1002/mds.21910

  3. Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features

    Movement Disorders

    Volume 20, Issue 6, June 2005, Pages: 665–673, Anne-Fleur Van Rootselaar, Ivo N. van Schaik, Arn M.J.M. van den Maagdenberg, Johannes H.T.M. Koelman, Petra M.C. Callenbach and Marina A.J. Tijssen

    Article first published online : 3 MAR 2005, DOI: 10.1002/mds.20413

  4. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

  5. Myoclonus in Creutzfeldt-Jakob disease: Polygraphic and video-electroencephalography assessment of 109 patients

    Movement Disorders

    Volume 25, Issue 16, 15 December 2010, Pages: 2818–2827, Simona Binelli, Pamela Agazzi, Laura Canafoglia, Vidmer Scaioli, Ferruccio Panzica, Elisa Visani, Giuseppe Di Fede, Giorgio Giaccone, Alberto Bizzi, Orso Bugiani, Guiliano Avanzini, Fabrizio Tagliavini and Silvana Franceschetti

    Article first published online : 11 OCT 2010, DOI: 10.1002/mds.23397

  6. Decreased cortical inhibition and yet cerebellar pathology in ‘familial cortical myoclonic tremor with epilepsy’

    Movement Disorders

    Volume 22, Issue 16, 15 December 2007, Pages: 2378–2385, Anne-Fleur van Rootselaar, Sandra M.A. van der Salm, Lo J. Bour, Mark J. Edwards, Peter Brown, Eleonora Aronica, Johanna M. Rozemuller-Kwakkel, Peter J. Koehler, Johannes H.T.M. Koelman, John C. Rothwell and Marina A.J. Tijssen

    Article first published online : 25 SEP 2007, DOI: 10.1002/mds.21738

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    Myoclonus–dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families

    Movement Disorders

    Volume 23, Issue 1, January 2008, Pages: 28–34, Nardo Nardocci, Giovanna Zorzi, Chiara Barzaghi, Federica Zibordi, Claudia Ciano, Daniele Ghezzi and Barbara Garavaglia

    Article first published online : 12 SEP 2007, DOI: 10.1002/mds.21715

  8. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Article first published online : 6 JUN 2014, DOI: 10.1002/mds.25914

  9. Abstracts

    Movement Disorders

    Volume 29, Issue S2, November 2014, Pages: S13–S101,

    Article first published online : 26 NOV 2014, DOI: 10.1002/mds.26090

  10. Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation

    Movement Disorders

    Volume 29, Issue 1, January 2014, Pages: 139–143, Martje E. van Egmond, Corien C. Verschuuren-Bemelmans, Esther A. Nibbeling, Jan Willem J. Elting, Deborah A. Sival, Oebele F. Brouwer, Jeroen J. de Vries, Hubertus P. Kremer, Richard J. Sinke, Marina A. Tijssen and Tom J. de Koning

    Article first published online : 30 OCT 2013, DOI: 10.1002/mds.25704

  11. RELN rare variants in myoclonus-dystonia

    Movement Disorders

    Justus L. Groen, Katja Ritz, Hamid Jalalzadeh, Sandra M.A. van der Salm, Aldo Jongejan, Olaf R. Mook, Martin A. Haagmans, Aeilko H. Zwinderman, Mahdi M. Motazacker, Raoul C. Hennekam, Frank Baas and Marina A.J. Tijssen

    Article first published online : 4 FEB 2015, DOI: 10.1002/mds.26070

  12. Pathology and sensitivity of current clinical criteria in corticobasal syndrome

    Movement Disorders

    Volume 29, Issue 2, February 2014, Pages: 238–244, Haruka Ouchi, Yasuko Toyoshima, Mari Tada, Mutsuo Oyake, Izumi Aida, Itsuro Tomita, Akira Satoh, Mitsuhiro Tsujihata, Hitoshi Takahashi, Masatoyo Nishizawa and Takayoshi Shimohata

    Article first published online : 20 NOV 2013, DOI: 10.1002/mds.25746

  13. Myoclonic tremulous movements in multiple system atrophy are a form of cortical myoclonus

    Movement Disorders

    Volume 20, Issue 4, April 2005, Pages: 451–456, Yasuyuki Okuma, Kenji Fujishima, Hideto Miwa, Hideo Mori and Yoshikuni Mizuno

    Article first published online : 9 DEC 2004, DOI: 10.1002/mds.20346

  14. The syndrome of deafness-dystonia: Clinical and genetic heterogeneity

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 795–803, Maja Kojovic, Isabel Pareés, Tania Lampreia, Karolina Pienczk-Reclawowicz, Georgia Xiromerisiou, Ignacio Rubio-Agusti, Milica Kramberger, Miryam Carecchio, Anas M. Alazami, Francesco Brancati, Jaroslaw Slawek, Zvezdan Pirtosek, Enza Maria Valente, Fowzan S. Alkuraya, Mark J. Edwards and Kailash P. Bhatia

    Article first published online : 15 FEB 2013, DOI: 10.1002/mds.25394

  15. Abnormal low frequency drive in myoclonus-dystonia patients correlates with presence of dystonia

    Movement Disorders

    Volume 22, Issue 9, 15 July 2007, Pages: 1299–1307, Elisabeth M. J. Foncke, Lo J. Bour, Johan N. van der Meer, Johannes H. T. M. Koelman and Marina A. J. Tijssen

    Article first published online : 7 MAY 2007, DOI: 10.1002/mds.21519

  16. Defining the Epsilon-Sarcoglycan (SGCE) Gene Phenotypic Signature in Myoclonus-Dystonia: A Reappraisal of Genetic Testing Criteria

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 787–794, Miryam Carecchio, Monia Magliozzi, Massimiliano Copetti, Alessandro Ferraris, Laura Bernardini, Monica Bonetti, Giovanni Defazio, Mark J. Edwards, Isabella Torrente, Fabio Pellegrini, Cristoforo Comi, Kailash P. Bhatia and Enza Maria Valente

    Article first published online : 15 MAY 2013, DOI: 10.1002/mds.25506

  17. Kufor Rakeb Disease: Autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia

    Movement Disorders

    Volume 20, Issue 10, October 2005, Pages: 1264–1271, David R. Williams, Ali Hadeed, Amir S. Najim al-Din, Abdel-Latif Wreikat and Andrew J. Lees

    Article first published online : 28 JUN 2005, DOI: 10.1002/mds.20511

  18. Myoclonus and dystonia in cerebrotendinous xanthomatosis

    Movement Disorders

    Volume 27, Issue 14, December 2012, Pages: 1805–1810, Julien Lagarde, Emmanuel Roze, Emmanuelle Apartis, Deepa Pothalil, Frédéric Sedel, Philippe Couvert, Marie Vidailhet and Bertrand Degos

    Article first published online : 31 OCT 2012, DOI: 10.1002/mds.25206

  19. A new familial syndrome with dystonia and lower limb action myoclonus

    Movement Disorders

    Volume 26, Issue 5, April 2011, Pages: 896–900, Justus Groen, Anne-Fleur van Rootselaar, Sandra M. A. van der Salm, Bastiaan R. Bloem and Marina Tijssen

    Article first published online : 2 MAR 2011, DOI: 10.1002/mds.23557

  20. Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype

    Movement Disorders

    Volume 21, Issue 3, March 2006, Pages: 396–401, Esther Brusse, Inge de Koning, Anneke Maat-Kievit, Ben A. Oostra, Peter Heutink and John C. van Swieten

    Article first published online : 6 OCT 2005, DOI: 10.1002/mds.20708