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There are 7659918 results for: content related to: Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. Poster session 4, Abstracts 1018–1073

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S349–S366,

    Version of Record online : 10 MAY 2004, DOI: 10.1002/mds.20180

  8. Dopa-responsive dystonia presenting with prominent isolated bilateral resting leg tremor: Evidence for a role of parkin?

    Movement Disorders

    Volume 18, Issue 9, September 2003, Pages: 1070–1072, Ronald B. Postuma, Yoshiaki Furukawa, Ekaterina Rogaeva, Peter H. St. George-Hyslop, Matt J. Farrer and Anthony E. Lang

    Version of Record online : 2 JUN 2003, DOI: 10.1002/mds.10478

  9. 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

  10. Immunohistochemical and subcellular localization of parkin protein: Absence of protein in autosomal recessive juvenile parkinsonism patients

    Annals of Neurology

    Volume 45, Issue 5, May 1999, Pages: 668–672, Hideki Shimura, Nobutaka Hattori, Shin-Ichiro Kubo, Mutsuko Yoshikawa, Tohru Kitada, Hiroto Matsumine, Shuichi Asakawa, Shinsei Minoshima, Yasuhiro Yamamura, Nobuyoshi Shimizu and Yoshikuni Mizuno

    Version of Record online : 1 JUN 2001, DOI: 10.1002/1531-8249(199905)45:5<668::AID-ANA19>3.0.CO;2-Z

  11. Autosomal recessive juvenile parkinsonism: A key to understanding nigral degeneration in sporadic Parkinson's disease

    Neuropathology

    Volume 20, Issue s1, September 2000, Pages: 85–90, Nobutaka Hattori, 1 Hideki Shimura, 1 Shin-ichiro Kubo, 1 Tohru Kitada, 1 Mei Wang, 1 Shuichi Asakawa, 2 Shinsei Minashima, 2 Nobuyoshi Shimizu, 2 Toshiaki Suzuki, 3 Keiji Tanaka and 3 Yoshikuni Mizuno 1

    Version of Record online : 4 JAN 2002, DOI: 10.1046/j.1440-1789.2000.00312.x

  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. Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

    Annals of Neurology

    Volume 48, Issue 2, August 2000, Pages: 245–250, Mieko Maruyama, Takeshi Ikeuchi, Masaaki Saito, Atsushi Ishikawa, Tatsuhiko Yuasa, Hajime Tanaka, Shintaro Hayashi, Koichi Wakabayashi, Hitoshi Takahashi and Shoji Tsuji

    Version of Record online : 4 APR 2001, DOI: 10.1002/1531-8249(200008)48:2<245::AID-ANA15>3.0.CO;2-2

  14. Dopa-responsive dystonia: Recent advances and remaining issues to be addressed

    Movement Disorders

    Volume 14, Issue 5, September 1999, Pages: 709–715, Yoshiaki Furukawa and Stephen J. Kish

    Version of Record online : 16 JAN 2001, DOI: 10.1002/1531-8257(199909)14:5<709::AID-MDS1001>3.0.CO;2-T

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    Advances in the Genetics of Parkinson's Disease: A Guide for the Clinician

    Movement Disorders Clinical Practice

    Volume 1, Issue 1, April 2014, Pages: 3–13, Una-Marie Sheerin, Henry Houlden and Nicholas W. Wood

    Version of Record online : 10 APR 2014, DOI: 10.1002/mdc3.12000

  16. 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

  17. Molecular analyses of GCH-1, TH and parkin genes in Chinese dopa-responsive dystonia families

    Clinical Genetics

    Volume 74, Issue 6, December 2008, Pages: 513–521, Z-Y Wu, Y Lin, W-J Chen, G-X Zhao, H Xie, S-X Murong and N Wang

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.2008.01039.x

  18. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals

    Annals of Neurology

    Volume 44, Issue 6, December 1998, Pages: 935–941, Nobutaka Hattori, Tohru Kitada, Hiroto Matsumine, Shuichi Asakawa, Yasuhiro Yamamura, Hiroyo Yoshino, Tomonori Kobayashi, Masayuki Yokochi, Mei Wang, Asako Yoritaka, Tomoyoshi Kondo, Shigeki Kuzuhara, Shigenobu Nakamura, Nobuyoshi Shimizu and Yoshikuni Mizuno

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410440612

  19. Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease

    European Journal of Neurology

    Volume 13, Issue 4, April 2006, Pages: 385–390, J. M. Hertz, K. Østergaard, I. Juncker, S. Pedersen, A. Romstad, L. B. Møller, F. Güttler and E. Dupont

    Version of Record online : 21 APR 2006, DOI: 10.1111/j.1468-1331.2006.01249.x

  20. How much phenotypic variation can be attributed to parkin genotype?

    Annals of Neurology

    Volume 54, Issue 2, August 2003, Pages: 176–185, Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, Nick W. Wood, Giuseppe De Michele, Anne-Marie Bonnet, Valérie Fraix, Emmanuel Broussolle, Martin W. I. M. Horstink, Marie Vidailhet, Patrice Verpillat, Thomas Gasser, David Nicholl, Hélio Teive, Salmo Raskin, Olivier Rascol, Alain Destée, Merle Ruberg, Francesca Gasparini, Giuseppe Meco, Yves Agid, Alexandra Durr and Alexis Brice

    Version of Record online : 30 MAY 2003, DOI: 10.1002/ana.10613