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There are 74714 results for: content related to: Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease

  1. 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

  2. Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease

    Clinical Genetics

    Volume 82, Issue 1, July 2012, Pages: 77–82, S Y Kim, M W Seong, B S Jeon, S Y Kim, H S Ko, J Y Kim and S S Park

    Version of Record online : 29 MAY 2011, DOI: 10.1111/j.1399-0004.2011.01693.x

  3. 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

  4. 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

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    Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients

    Human Mutation

    Volume 23, Issue 5, May 2004, Page: 525, Ana Djarmati, Katja Hedrich, Marina Svetel, Nora Schäfer, Vladislava Juric, Slobodanka Vukosavic, Robert Hering, Olaf Riess, Stanka Romac, Christine Klein and Vladimir Kostic

    Version of Record online : 31 MAR 2004, DOI: 10.1002/humu.9240

  6. High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1047–1051, Jorge Luis Guerrero Camacho, Nancy Monroy Jaramillo, Petra Yescas Gómez, Mayela Rodríguez Violante, Catherine Boll Woehrlen, Ma. Elisa Alonso Vilatela and Marisol López López

    Version of Record online : 6 JUL 2012, DOI: 10.1002/mds.25030

  7. High-Resolution Survey in Familial Parkinson Disease Genes Reveals Multiple Independent Copy Number Variation Events in PARK2

    Human Mutation

    Volume 34, Issue 8, August 2013, Pages: 1071–1074, Liyong Wang, Karen Nuytemans, Guney Bademci, Cherylyn Jauregui, Eden R. Martin, William K. Scott, Jeffery M. Vance and Stephan Zuchner

    Version of Record online : 28 MAY 2013, DOI: 10.1002/humu.22344

  8. 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

  9. Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinoma

    Genes, Chromosomes and Cancer

    Volume 51, Issue 5, May 2012, Pages: 462–472, Reika Iwakawa, Hirokazu Okayama, Takashi Kohno, Aiko Sato-Otsubo, Seishi Ogawa and Jun Yokota

    Version of Record online : 3 FEB 2012, DOI: 10.1002/gcc.21933

  10. 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

  11. Pathogenic mutations in Parkinson disease

    Human Mutation

    Volume 28, Issue 7, July 2007, Pages: 641–653, Eng-King Tan and Lisa M. Skipper

    Version of Record online : 26 MAR 2007, DOI: 10.1002/humu.20507

  12. Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease

    Movement Disorders

    Volume 27, Issue 12, October 2012, Pages: 1522–1529, Laura L. Kilarski, Justin P. Pearson, Victoria Newsway, Elisa Majounie, M. Duleeka W. Knipe, Anjum Misbahuddin, Patrick F. Chinnery, David J. Burn, Carl E. Clarke, Marie-Helene Marion, Alistair J. Lewthwaite, David J. Nicholl, Nicholas W. Wood, Karen E. Morrison, Caroline H. Williams-Gray, Jonathan R. Evans, Stephen J. Sawcer, Roger A. Barker, Mirdhu M. Wickremaratchi, Yoav Ben-Shlomo, Nigel M. Williams and Huw R. Morris

    Version of Record online : 6 SEP 2012, DOI: 10.1002/mds.25132

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    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

  14. 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

  15. Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

    Human Mutation

    Volume 30, Issue 7, July 2009, Pages: 1054–1061, Karen Nuytemans, Bram Meeus, David Crosiers, Nathalie Brouwers, Dirk Goossens, Sebastiaan Engelborghs, Philippe Pals, Barbara Pickut, Marleen Van den Broeck, Ellen Corsmit, Patrick Cras, Peter P. De Deyn, Jurgen Del-Favero, Christine Van Broeckhoven and Jessie Theuns

    Version of Record online : 3 MAR 2009, DOI: 10.1002/humu.21007

  16. Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 1, January 2010, Pages: 229–234, Yih-Ru Wu, Chun-Hsien Wu, Chih-Ying Chao, Chun-Chieh Kuan, Wan-Ling Zhang, Cheng-Kuang Wang, Chun-Yuh Chang, Yi-Chun Chang, Guey-Jen Lee-Chen and Chung-Mei Chen

    Version of Record online : 27 MAY 2009, DOI: 10.1002/ajmg.b.30977

  17. Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism

    Human Mutation

    Volume 28, Issue 1, January 2007, Pages: 27–32, Suzanne Lesage, Periquet Magali, Ebba Lohmann, Lucette Lacomblez, Helio Teive, Sabine Janin, Pierre-Yves Cousin, Alexandra Dürr and Alexis Brice

    Version of Record online : 26 OCT 2006, DOI: 10.1002/humu.20436

  18. Genetic mutations in early-onset Parkinson's disease Mexican patients: Molecular testing implications

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 3, April 2014, Pages: 235–244, Nancy Monroy-Jaramillo, Jorge Luis Guerrero-Camacho, Mayela Rodríguez-Violante, Marie-Catherine Boll-Woehrlen, Petra Yescas-Gómez, María Elisa Alonso-Vilatela and Marisol López-López

    Version of Record online : 23 FEB 2014, DOI: 10.1002/ajmg.b.32228

  19. Structural and Functional Impact of Parkinson Disease-Associated Mutations in the E3 Ubiquitin Ligase Parkin

    Human Mutation

    Volume 36, Issue 8, August 2015, Pages: 774–786, Fabienne C. Fiesel, Thomas R. Caulfield, Elisabeth L. Moussaud-Lamodière, Kotaro Ogaki, Daniel F.A.R. Dourado, Samuel C. Flores, Owen A. Ross and Wolfdieter Springer

    Version of Record online : 3 JUN 2015, DOI: 10.1002/humu.22808

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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