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There are 1905658 results for: content related to: A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease

  1. You have free access to this content
    Leucine-rich repeat kinase 2 regulates Sec16A at ER exit sites to allow ER–Golgi export

    The EMBO Journal

    Volume 33, Issue 20, 16 October 2014, Pages: 2314–2331, Hyun Jin Cho, Jia Yu, Chengsong Xie, Parvathi Rudrabhatla, Xi Chen, Junbing Wu, Loukia Parisiadou, Guoxiang Liu, Lixin Sun, Bo Ma, Jinhui Ding, Zhihua Liu and Huaibin Cai

    Version of Record online : 8 SEP 2014, DOI: 10.15252/embj.201487807

  2. Motor and nonmotor heterogeneity of LRRK2-related and idiopathic Parkinson's disease

    Movement Disorders

    Connie Marras, Roy N. Alcalay, Chelsea Caspell-Garcia, Christopher Coffey, Piu Chan, John E. Duda, Maurizio F. Facheris, Rubén Fernández-Santiago, Javier Ruíz-Martínez, Tiago Mestre, Rachel Saunders-Pullman, Claustre Pont-Sunyer, Eduardo Tolosa, Bjorg Waro and the LRRK2 Cohort Consortium

    Version of Record online : 19 APR 2016, DOI: 10.1002/mds.26614

  3. You have full text access to this OnlineOpen article
    Novel recruitment strategy to enrich for LRRK2 mutation carriers

    Molecular Genetics & Genomic Medicine

    Volume 3, Issue 5, September 2015, Pages: 404–412, Tatiana Foroud, Danielle Smith, Jacqueline Jackson, Jennifer Verbrugge, Cheryl Halter, Leah Wetherill, Katherine Sims, Winnie Xin, Vanessa Arnedo, Shirley Lasch, Kenneth Marek and the Parkinson's Progression Markers Initiative

    Version of Record online : 6 MAY 2015, DOI: 10.1002/mgg3.151

  4. Increased peripheral inflammation in asymptomatic leucine-rich repeat kinase 2 mutation carriers

    Movement Disorders

    Nicolas Dzamko, Dominic B. Rowe and Glenda M. Halliday

    Version of Record online : 25 FEB 2016, DOI: 10.1002/mds.26529

  5. Leucine-rich repeat kinase 2 and alternative splicing in Parkinson's disease

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1004–1011, David A. Elliott, Woojin S. Kim, Sarsha Gorissen, Glenda M. Halliday and John B.J. Kwok

    Version of Record online : 23 APR 2012, DOI: 10.1002/mds.25005

  6. A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia

    European Journal of Neurology

    Volume 14, Issue 4, April 2007, Pages: 413–417, S. N. Illarioshkin, M. I. Shadrina, P. A. Slominsky, E. V. Bespalova, T. B. Zagorovskaya, G. Kh. Bagyeva, E. D. Markova, S. A. Limborska and I. A. Ivanova-Smolenskaya

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1468-1331.2007.01685.x

  7. LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2536–2541, Rachel Saunders-Pullman, Matthew J. Barrett, Kaili M. Stanley, Marta San Luciano, Vicki Shanker, Lawrence Severt, Ann Hunt, Deborah Raymond, Laurie J. Ozelius and Susan B. Bressman

    Version of Record online : 3 SEP 2010, DOI: 10.1002/mds.23314

  8. Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriers

    Movement Disorders

    Dolores Vilas, Leslie M. Shaw, Peggy Taylor, Daniela Berg, Kathrin Brockmann, Jan Aasly, Connie Marras, Claustre Pont-Sunyer, José Ríos, Ken Marek and Eduardo Tolosa

    Version of Record online : 4 APR 2016, DOI: 10.1002/mds.26591

  9. You have free access to this content
    Leucine-rich repeat kinase 2 disturbs mitochondrial dynamics via Dynamin-like protein

    Journal of Neurochemistry

    Volume 122, Issue 3, August 2012, Pages: 650–658, Jingwen Niu, Mei Yu, Chunyan Wang and Zhiheng Xu

    Version of Record online : 22 JUN 2012, DOI: 10.1111/j.1471-4159.2012.07809.x

  10. You have full text access to this OnlineOpen article
    Cellular processes associated with LRRK2 function and dysfunction

    The FEBS Journal

    Volume 282, Issue 15, August 2015, Pages: 2806–2826, Rebecca Wallings, Claudia Manzoni and Rina Bandopadhyay

    Version of Record online : 9 MAY 2015, DOI: 10.1111/febs.13305

  11. Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations

    Movement Disorders

    Volume 26, Issue 11, September 2011, Pages: 2026–2031, Javier Ruiz-Martínez, Ana Gorostidi, Estibaliz Goyenechea, Ainhoa Alzualde, Juan José Poza, Francisco Rodríguez, Alberto Bergareche, Fermín Moreno, Adolfo López de Munain and José F. Martí Massó

    Version of Record online : 24 MAY 2011, DOI: 10.1002/mds.23773

  12. High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal

    Movement Disorders

    Volume 22, Issue 8, 15 June 2007, Pages: 1194–1201, Joaquim J. Ferreira, Leonor Correia Guedes, Mário Miguel Rosa, Miguel Coelho, Marina van Doeselaar, Dorothea Schweiger, Alessio Di Fonzo, Ben A. Oostra, Cristina Sampaio and Vincenzo Bonifati

    Version of Record online : 27 APR 2007, DOI: 10.1002/mds.21525

  13. Striatal leucine-rich repeat kinase 2 mRNA is increased in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned common marmosets (Callithrix jacchus) with l-3, 4-dihydroxyphenylalanine methyl ester-induced dyskinesia

    European Journal of Neuroscience

    Volume 26, Issue 1, July 2007, Pages: 171–177, M. J. Hurley, P. H. Patel, M. J. Jackson, L. A. Smith, S. Rose and P. Jenner

    Version of Record online : 3 JUL 2007, DOI: 10.1111/j.1460-9568.2007.05638.x

  14. LRRK2 and Parkinson’s disease in Norway

    Acta Neurologica Scandinavica

    Volume 115, Issue s187, May 2007, Pages: 72–75, M. Toft, K. Haugarvoll, O. A. Ross, M. J. Farrer and J. O. Aasly

    Version of Record online : 29 MAR 2007, DOI: 10.1111/j.1600-0404.2007.00852.x

  15. Prevalence and clinical features of LRRK2 mutations in patients with Parkinson’s disease in southern Spain

    European Journal of Neurology

    Volume 16, Issue 8, August 2009, Pages: 957–960, L. Gao, P. Gómez-Garre, F. J. Díaz-Corrales, F. Carrillo, M. Carballo, A. Palomino, J. Díaz-Martín, R. Mejías, P. J. Vime, J. López-Barneo and P. Mir

    Version of Record online : 31 MAR 2009, DOI: 10.1111/j.1468-1331.2009.02620.x

  16. Screening for LRRK2 mutations in patients with Parkinson’s disease in Russia: identification of a novel LRRK2 variant

    European Journal of Neurology

    Volume 15, Issue 7, July 2008, Pages: 692–696, S. N. Pchelina, A. F. Yakimovskii, A. K. Emelyanov, O. N. Ivanova, A. L. Schwarzman and A. B. Singleton

    Version of Record online : 24 APR 2008, DOI: 10.1111/j.1468-1331.2008.02149.x

  17. 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

  18. Low-variance RNAs identify Parkinson's disease molecular signature in blood

    Movement Disorders

    Volume 30, Issue 6, May 2015, Pages: 813–821, Maria D. Chikina, Christophe P. Gerald, Xianting Li, Yongchao Ge, Hanna Pincas, Venugopalan D. Nair, Aaron K. Wong, Arjun Krishnan, Olga G. Troyanskaya, Deborah Raymond, Rachel Saunders-Pullman, Susan B. Bressman, Zhenyu Yue and Stuart C. Sealfon

    Version of Record online : 18 MAR 2015, DOI: 10.1002/mds.26205

  19. You have free access to this content
    LRRK2 in Parkinson’s disease: in vivo models and approaches for understanding pathogenic roles

    The FEBS Journal

    Volume 276, Issue 22, November 2009, Pages: 6445–6454, Zhenyu Yue

    Version of Record online : 5 OCT 2009, DOI: 10.1111/j.1742-4658.2009.07343.x

  20. Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe

    Human Mutation

    Volume 33, Issue 7, July 2012, Pages: 1087–1098, Justin P. Rubio, Simon Topp, Liling Warren, Pamela L. St. Jean, Daniel Wegmann, Darren Kessner, John Novembre, Judong Shen, Dana Fraser, Jennifer Aponte, Keith Nangle, Lon R. Cardon, Margaret G. Ehm, Stephanie L. Chissoe, John C. Whittaker, Matthew R. Nelson and Vincent E. Mooser

    Version of Record online : 4 APR 2012, DOI: 10.1002/humu.22075