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There are 5971916 results for: content related to: Commentary for “Slowing of saccadic eye movements in sporadic Creutzfeldt-Jakob disease”

  1. Slowing of saccadic eye movements in sporadic Creutzfeldt–Jakob disease

    Movement Disorders

    Volume 28, Issue 3, March 2013, Pages: 291–293, Niels Fockaert, Marc Van Orshoven, Patrick Cras, Christine Van Broeckhoven, Philippe Demaerel and Wim Vandenberghe

    Version of Record online : 21 MAR 2013, DOI: 10.1002/mds.25384

  2. 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

  3. 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

  4. “Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy—A diagnostic guide

    Movement Disorders

    Volume 28, Issue 9, August 2013, Pages: 1184–1199, Maria Stamelou, Niall P. Quinn and Kailash P. Bhatia

    Version of Record online : 29 MAY 2013, DOI: 10.1002/mds.25509

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    List of Abstracts

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S524–S592,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25052

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    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

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    Abstracts

    Movement Disorders

    Volume 32, Issue S2, June 2017, Pages: S1–S627,

    Version of Record online : 2 JUN 2017, DOI: 10.1002/mds.27087

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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

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    Imaging of prion diseases

    Journal of Magnetic Resonance Imaging

    Volume 35, Issue 5, May 2012, Pages: 998–1012, Laurent Letourneau-Guillon, Ryan Wada and Walter Kucharczyk

    Version of Record online : 12 APR 2012, DOI: 10.1002/jmri.23504

  10. Prion diseases in man

    The Journal of Pathology

    Volume 186, Issue 3, November 1998, Pages: 227–234, James W. Ironside

    Version of Record online : 15 OCT 1999, DOI: 10.1002/(SICI)1096-9896(1998110)186:3<227::AID-PATH174>3.0.CO;2-3

  11. Review: Creutzfeldt–Jakob disease: prion protein type, disease phenotype and agent strain

    Neuropathology and Applied Neurobiology

    Volume 38, Issue 4, June 2012, Pages: 296–310, M. W. Head and J. W. Ironside

    Version of Record online : 11 MAY 2012, DOI: 10.1111/j.1365-2990.2012.01265.x

  12. Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease

    Neuropathology

    Volume 27, Issue 5, October 2007, Pages: 434–441, Yasushi Iwasaki, Mari Yoshida, Yoshio Hashizume, Tetsuyuki Kitamoto and Gen Sobue

    Version of Record online : 18 SEP 2007, DOI: 10.1111/j.1440-1789.2007.00812.x

  13. Human Prion Diseases

    Principles and Practice of Clinical Virology, Sixth Edition

    Arie J. Zuckerman, Jangu E. Banatvala, Barry D. Schoub, Paul D. Griffiths, Philip Mortimer, Pages: 939–968, 2009

    Published Online : 16 MAR 2009, DOI: 10.1002/9780470741405.ch39

  14. The spatial pattern of the vacuolation (‘spongiform change’) in the cerebral cortex in variant Creutzfeldt-Jakob disease (vCJD)

    Neuroscience Research Communications

    Volume 30, Issue 1, January/February 2002, Pages: 43–50, R. A. Armstrong, N. J. Cairns, J. W. Ironside and P. L. Lantos

    Version of Record online : 28 FEB 2002, DOI: 10.1002/nrc.10016

  15. Genetic Creutzfeldt–Jakob Disease

    Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders, Second Edition

    Piero Parchi, Pierluigi Gambetti, Sabina Capellari, Pages: 336–345, 2011

    Published Online : 21 SEP 2011, DOI: 10.1002/9781444341256.ch33

  16. Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt–Jakob disease

    Neuropathology and Applied Neurobiology

    Volume 26, Issue 5, October 2000, Pages: 463–472, G. G. Kovacs, M. W. Head, T. Bunn, L. Laszlo, R. G. Will and J. W. Ironside

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1365-2990.2000.00279.x

  17. Human Prion Diseases

    Principles and Practice of Clinical Virology, Fifth Edition

    Arie J. Zuckerman, Jangu E. Banatvala, John R. Pattison, Paul D. Griffiths, Barry D. Schoub, Pages: 779–811, 2004

    Published Online : 21 JUL 2004, DOI: 10.1002/0470020970.ch26

  18. PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease

    Microscopy Research and Technique

    Volume 50, Issue 1, 1 July 2000, Pages: 26–31, Nicolas Privat, Véronique Sazdovitch, Danielle Seilhean, Jean-Louis LaPlanche and Jean-Jacques Hauw

    Version of Record online : 22 JUN 2000, DOI: 10.1002/1097-0029(20000701)50:1<26::AID-JEMT5>3.0.CO;2-S

  19. Prion protein heterogeneity in sporadic but not variant Creutzfeldt–Jakob disease: U.K. cases 1991–2002

    Annals of Neurology

    Volume 55, Issue 6, June 2004, Pages: 851–859, Mark W. Head, Tristan J. R. Bunn, Matthew T. Bishop, Victoria McLoughlin, Suzanne Lowrie, Clive S. McKimmie, Michelle C. Williams, Linda McCardle, Jan MacKenzie, Richard Knight, Robert G. Will and James W. Ironside

    Version of Record online : 27 MAY 2004, DOI: 10.1002/ana.20127

  20. Preclinical sporadic Creutzfeldt-Jakob disease in French blood donors: an epidemiologic model-based study

    Transfusion

    Volume 52, Issue 6, June 2012, Pages: 1290–1295, Josiane Pillonel, Jean-Philippe Brandel, Lucie Léon, Dominique Salomon, Stéphane Haïk, Isabelle Capek, Véronique Vaillant, Joliette Coste and Annick Alpérovitch

    Version of Record online : 1 DEC 2011, DOI: 10.1111/j.1537-2995.2011.03459.x