Search Results

There are 32061 results for: content related to: Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations

  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. 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

  3. 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

  4. 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

  5. Novel parkin mutations detected in patients with early-onset Parkinson's disease

    Movement Disorders

    Volume 20, Issue 4, April 2005, Pages: 424–431, Aida M. Bertoli-Avella, José L. Giroud-Benitez, Ali Akyol, Egberto Barbosa, Onno Schaap, Herma C. van der Linde, Emilia Martignoni, Leonardo Lopiano, Paolo Lamberti, Emiliana Fincati, Angelo Antonini, Fabrizio Stocchi, Pasquale Montagna, Ferdinando Squitieri, Paolo Marini, Giovanni Abbruzzese, Giovanni Fabbrini, Roberto Marconi, Alessio Dalla Libera, Giorgio Trianni, Marco Guidi, Antonio De Gaetano, Gustavo Boff Maegawa, Antonino De Leo, Virgilio Gallai, Giulia de Rosa, Nicola Vanacore, Giuseppe Meco, Cornelia M. van Duijn, Ben A. Oostra, Peter Heutink and Vincenzo Bonifati

    Version of Record online : 6 DEC 2004, DOI: 10.1002/mds.20343

  6. You have free access to this content
    14-3-3η is a novel regulator of parkin ubiquitin ligase

    The EMBO Journal

    Volume 25, Issue 1, January 11, 2006, Pages: 211–221, Shigeto Sato, Tomoki Chiba, Eri Sakata, Koichi Kato, Yoshikuni Mizuno, Nobutaka Hattori and Keiji Tanaka

    Version of Record online : 11 AUG 2005, DOI: 10.1038/sj.emboj.7600774

  7. 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

  8. You have free access to this content
    Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences

    The EMBO Journal

    Volume 31, Issue 14, July 18, 2012, Pages: 3038–3062, Nicole Exner, Anne Kathrin Lutz, Christian Haass and Konstanze F Winklhofer

    Version of Record online : 26 JUN 2012, DOI: 10.1038/emboj.2012.170

  9. You have free access to this content
    Identification and characterization of a novel endogenous murine parkin mutation

    Journal of Neurochemistry

    Volume 113, Issue 2, April 2010, Pages: 402–417, Chenere P. Ramsey and Benoit I. Giasson

    Version of Record online : 20 JAN 2010, DOI: 10.1111/j.1471-4159.2010.06605.x

  10. Restless legs syndrome, rapid eye movement sleep behavior disorder, and hypersomnia in patients with two parkin mutations

    Movement Disorders

    Volume 24, Issue 13, 15 October 2009, Pages: 1970–1976, Nadège Limousin, Eric Konofal, Elias Karroum, Ebba Lohmann, Ioannis Theodorou, Alexandra Dürr and Isabelle Arnulf

    Version of Record online : 11 AUG 2009, DOI: 10.1002/mds.22711

  11. Reduction in endogenous parkin levels renders glial cells sensitive to both caspase-dependent and caspase-independent cell death

    European Journal of Neuroscience

    Volume 20, Issue 8, October 2004, Pages: 2038–2048, Luci P. MacCormac, Miratul M. K. Muqit, David J. Faulkes, Nicholas W. Wood and David S. Latchman

    Version of Record online : 14 SEP 2004, DOI: 10.1111/j.1460-9568.2004.03659.x

  12. Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations

    Movement Disorders

    Volume 19, Issue 5, May 2004, Pages: 544–548, Meltem Müftüoglu, Bülent Elibol, Özlem Dalmızrak, Ayse Ercan, Gülnihal Kulaksız, Hamdi Ögüs, Turgay Dalkara and Nazmi Özer

    Version of Record online : 15 DEC 2003, DOI: 10.1002/mds.10695

  13. You have full text access to this OnlineOpen article
    Parkin occurs in a stable, non-covalent, ∼110-kDa complex in brain

    European Journal of Neuroscience

    Volume 27, Issue 2, January 2008, Pages: 284–293, Cindy Van Humbeeck, Etienne Waelkens, Olga Corti, Alexis Brice and Wim Vandenberghe

    Version of Record online : 10 JAN 2008, DOI: 10.1111/j.1460-9568.2007.06000.x

  14. parkin mutation analysis in clinic patients with early-onset Parkinson's disease

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 1, 15 August 2004, Pages: 44–50, P. Poorkaj, J. G. Nutt, D. James, S. Gancher, T. D. Bird, E. Steinbart, G. D. Schellenberg and Haydeh Payami

    Version of Record online : 7 JUN 2004, DOI: 10.1002/ajmg.a.30157

  15. You have free access to this content
    Alterations in the solubility and intracellular localization of parkin by several familial Parkinson's disease-linked point mutations

    Journal of Neurochemistry

    Volume 93, Issue 2, April 2005, Pages: 422–431, Cheng Wang, ,,,1 Jeanne M. M. Tan, ,1 Michelle W. L. Ho, Norazean Zaiden, Siew Heng Wong, Constance L. C. Chew, Pei Woon Eng, Tit Meng Lim, Ted M. Dawson and Kah Leong Lim,

    Version of Record online : 2 MAR 2005, DOI: 10.1111/j.1471-4159.2005.03023.x

  16. Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers

    Annals of Neurology

    Volume 58, Issue 3, September 2005, Pages: 411–422, Peter P. Pramstaller, Michael G. Schlossmacher, Thomas S. Jacques, Francesco Scaravilli, Cordula Eskelson, Imelda Pepivani, Katja Hedrich, Susanna Adel, Melissa Gonzales-McNeal, Rüdiger Hilker, Patricia L. Kramer and Christine Klein

    Version of Record online : 29 AUG 2005, DOI: 10.1002/ana.20587

  17. You have free access to this content
    How does parkin ligate ubiquitin to Parkinson's disease?

    EMBO reports

    Volume 5, Issue 7, July 2004, Pages: 681–685, Philipp J Kahle and Christian Haass

    Version of Record online : 1 JUL 2004, DOI: 10.1038/sj.embor.7400188

  18. Dyrk1A phosphorylates parkin at Ser-131 and negatively regulates its ubiquitin E3 ligase activity

    Journal of Neurochemistry

    Volume 134, Issue 4, August 2015, Pages: 756–768, Eunju Im and Kwang Chul Chung

    Version of Record online : 3 JUN 2015, DOI: 10.1111/jnc.13164

  19. Functional modulation of parkin through physical interaction with SUMO-1

    Journal of Neuroscience Research

    Volume 84, Issue 7, 15 November 2006, Pages: 1543–1554, Ji Won Um and Kwang Chul Chung

    Version of Record online : 5 SEP 2006, DOI: 10.1002/jnr.21041

  20. You have free access to this content
    Parkin mediates the degradation-independent ubiquitination of Hsp70

    Journal of Neurochemistry

    Volume 105, Issue 5, June 2008, Pages: 1806–1819, Darren J. Moore, Andrew B. West, Dustin A. Dikeman, Valina L. Dawson and Ted M. Dawson

    Version of Record online : 1 FEB 2008, DOI: 10.1111/j.1471-4159.2008.05261.x