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There are 7931249 results for: content related to: Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation

  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. 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

  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. You have free access to this content
    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

  5. 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

  6. You have free access to this content
    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

  7. Poster Session 3

    Movement Disorders

    Volume 21, Issue S15, September 2006, Pages: S517–S613,

    Version of Record online : 20 SEP 2006, DOI: 10.1002/mds.21248

  8. Poster session 1: A. Basic science, genetics, neuropharmacology, Parkinson's Disease

    Movement Disorders

    Volume 17, Issue S5, November 2002, Pages: S17–S64,

    Version of Record online : 21 OCT 2002, DOI: 10.1002/mds.10349

  9. An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene

    Movement Disorders

    Volume 15, Issue 5, September 2000, Pages: 884–888, Shintaro Hayashi, Koichi Wakabayashi, Atsushi Ishikawa, Hiroko Nagai, Masaaki Saito, Mieko Maruyama, Toshiaki Takahashi, Tetsutaro Ozawa, Shoji Tsuji and Hitoshi Takahashi

    Version of Record online : 23 JAN 2001, DOI: 10.1002/1531-8257(200009)15:5<884::AID-MDS1019>3.0.CO;2-8

  10. Diagnostic considerations in juvenile parkinsonism

    Movement Disorders

    Volume 19, Issue 2, February 2004, Pages: 123–135, Dominic C. Paviour, Robert A.H. Surtees and Andrew J. Lees

    Version of Record online : 12 NOV 2003, DOI: 10.1002/mds.10644

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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

  12. Poster Session 1

    Movement Disorders

    Volume 21, Issue S15, September 2006, Pages: S329–S424,

    Version of Record online : 20 SEP 2006, DOI: 10.1002/mds.21246

  13. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

    Movement Disorders

    Volume 18, Issue 8, August 2003, Pages: 914–919, Sergei N. Illarioshkin, Magali Periquet, Nina Rawal, Christoph B. Lücking, Tatyana B. Zagorovskaya, Pyotr A. Slominsky, Olga V. Miloserdova, Elena D. Markova, Svetlana A. Limborska, Irina A. Ivanova-Smolenskaya and Alexis Brice

    Version of Record online : 28 MAR 2003, DOI: 10.1002/mds.10467

  14. Lewy bodies and parkinsonism in families with parkin mutations

    Annals of Neurology

    Volume 50, Issue 3, September 2001, Pages: 293–300, Matt Farrer, Piu Chan, Rong Chen, Louis Tan, Sarah Lincoln, Dena Hernandez, Lysia Forno, Katrina Gwinn-Hardy, Leonard Petrucelli, Jennifer Hussey, Andrew Singleton, Caroline Tanner, John Hardy and J. William Langston

    Version of Record online : 3 AUG 2001, DOI: 10.1002/ana.1132

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    The long journey to the discovery of PARK2

    Neuropathology

    Volume 30, Issue 5, October 2010, Pages: 495–500, Yasuhiro Yamamura

    Version of Record online : 27 JUL 2010, DOI: 10.1111/j.1440-1789.2010.01144.x

  16. Hereditary parkinsonism: Parkinson disease look-alikes—An algorithm for clinicians to “PARK” genes and beyond

    Movement Disorders

    Volume 24, Issue 14, 30 October 2009, Pages: 2042–2058, Christine Klein, Susanne A. Schneider and Anthony E. Lang

    Version of Record online : 4 SEP 2009, DOI: 10.1002/mds.22675

  17. Poster session 3: Parkinson's Disease

    Movement Disorders

    Volume 17, Issue S5, November 2002, Pages: S115–S165,

    Version of Record online : 21 OCT 2002, DOI: 10.1002/mds.10351

  18. Probable Cornelia de Lange syndrome with progressive parkinsonism and dystonia

    Movement Disorders

    Volume 15, Issue 4, July 2000, Pages: 749–751, Hubert H. Fernandez, Joseph H. Friedman and Edward V. Famiglietti

    Version of Record online : 31 JAN 2001, DOI: 10.1002/1531-8257(200007)15:4<749::AID-MDS1028>3.0.CO;2-P

  19. Poster Session 2

    Movement Disorders

    Volume 21, Issue S15, September 2006, Pages: S425–S516,

    Version of Record online : 20 SEP 2006, DOI: 10.1002/mds.21247

  20. Complex relationship between Parkin mutations and Parkinson disease

    American Journal of Medical Genetics

    Volume 114, Issue 5, 8 July 2002, Pages: 584–591, Andrew West, Magali Periquet, Sarah Lincoln, Christoph B. Lücking, David Nicholl, Vincenzo Bonifati, Nina Rawal, Thomas Gasser, Ebba Lohmann, Jean-François Deleuze, Demetrius Maraganore, Allan Levey, Nick Wood, Alexandra Dürr, John Hardy, Alexis Brice and Matt Farrer

    Version of Record online : 10 MAY 2002, DOI: 10.1002/ajmg.10525