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There are 1784808 results for: content related to: Expanding the clinical phenotype of SNCA duplication carriers

  1. Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

    Annals of Neurology

    Volume 69, Issue 5, May 2011, Pages: 778–792, Alexis Elbaz, Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto-Ortolaza, Frédéric Moisan, Jan Aasly, Grazia Annesi, Maria Bozi, Laura Brighina, Marie-Christine Chartier-Harlin, Alain Destée, Carlo Ferrarese, Alessandro Ferraris, J. Mark Gibson, Suzana Gispert, Georgios M. Hadjigeorgiou, Barbara Jasinska-Myga, Christine Klein, Rejko Krüger, Jean-Charles Lambert, Katja Lohmann, Simone van de Loo, Marie-Anne Loriot, Timothy Lynch, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Leonidas Stefanis, Ryan J. Uitti, Enza Maria Valente, Carles Vilariño-Güell, Karin Wirdefeldt, Zbigniew K. Wszolek, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer and on behalf of the Genetic Epidemiology of Parkinson's Disease (GEO-PD) consortium

    Version of Record online : 9 MAR 2011, DOI: 10.1002/ana.22321

  2. A case of α-synuclein gene duplication presenting with head-shaking movements

    Movement Disorders

    Volume 28, Issue 3, March 2013, Pages: 384–387, Kaori Itokawa, Takeshi Sekine, Manabu Funayama, Hiroyuki Tomiyama, Miki Fukui, Toshimasa Yamamoto, Naotoshi Tamura, Hiroshi Matsuda, Nobutaka Hattori and Nobuo Araki

    Version of Record online : 2 NOV 2012, DOI: 10.1002/mds.25243

  3. SNCA variants are associated with increased risk for multiple system atrophy

    Annals of Neurology

    Volume 65, Issue 5, May 2009, Pages: 610–614, Sonja W. Scholz, Henry Houlden, Claudia Schulte, Manu Sharma, Abi Li, Daniela Berg, Anna Melchers, Reema Paudel, J. Raphael Gibbs, Javier Simon-Sanchez, Coro Paisan-Ruiz, Jose Bras, Jinhui Ding, Honglei Chen, Bryan J. Traynor, Sampath Arepalli, Ryan R. Zonozi, Tamas Revesz, Janice Holton, Nick Wood, Andrew Lees, Wolfgang Oertel, Ullrich Wüllner, Stefano Goldwurm, Maria Teresa Pellecchia, Thomas Illig, Olaf Riess, Hubert H. Fernandez, Ramon L. Rodriguez, Michael S. Okun, Werner Poewe, Gregor K. Wenning, John A. Hardy, Andrew B. Singleton and Thomas Gasser

    Version of Record online : 18 MAR 2009, DOI: 10.1002/ana.21685

  4. Alpha-synuclein repeat variants and survival in Parkinson's disease

    Movement Disorders

    Volume 29, Issue 8, July 2014, Pages: 1053–1057, Sun Ju Chung, Joanna M. Biernacka, Sebastian M. Armasu, Kari Anderson, Roberta Frigerio, Jan O. Aasly, Grazia Annesi, Anna Rita Bentivoglio, Laura Brighina, Marie-Christine Chartier-Harlin, Stefano Goldwurm, Georgios Hadjigeorgiou, Barbara Jasinska-Myga, Beom Seok Jeon, Yun Joong Kim, Rejko Krüger, Suzanne Lesage, Katerina Markopoulou, George Mellick, Karen E. Morrison, Andreas Puschmann, Eng-King Tan, David Crosiers, Jessie Theuns, Christine Van Broeckhoven, Karin Wirdefeldt, Zbigniew K. Wszolek, Alexis Elbaz, Demetrius M. Maraganore and on behalf of the Genetic Epidemiology of Parkinson's Disease Consortium

    Version of Record online : 27 FEB 2014, DOI: 10.1002/mds.25841

  5. Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease

    Annals of Neurology

    Volume 59, Issue 2, February 2006, Pages: 298–309, Kenya Nishioka, Shin Hayashi, Matthew J. Farrer, Andrew B. Singleton, Hiroyo Yoshino, Hisamasa Imai, Toshiaki Kitami, Kenichi Sato, Ryu Kuroda, Hiroyuki Tomiyama, Koichi Mizoguchi, Miho Murata, Tatsushi Toda, Issei Imoto, Johji Inazawa, Yoshikuni Mizuno and Nobutaka Hattori

    Version of Record online : 15 DEC 2005, DOI: 10.1002/ana.20753

  6. Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2

    Annals of Neurology

    Volume 71, Issue 3, March 2012, Pages: 370–384, Nathan Pankratz, Gary W. Beecham, Anita L. DeStefano, Ted M. Dawson, Kimberly F. Doheny, Stewart A. Factor, Taye H. Hamza, Albert Y. Hung, Bradley T. Hyman, Adrian J. Ivinson, Dmitri Krainc, Jeanne C. Latourelle, Lorraine N. Clark, Karen Marder, Eden R. Martin, Richard Mayeux, Owen A. Ross, Clemens R. Scherzer, David K. Simon, Caroline Tanner, Jeffery M. Vance, Zbigniew K. Wszolek, Cyrus P. Zabetian, Richard H. Myers, Haydeh Payami, William K. Scott, Tatiana Foroud and and the PD GWAS Consortium

    Version of Record online : 23 MAR 2012, DOI: 10.1002/ana.22687

  7. Neurofibrillary tau pathology modulated by genetic variation of α-synuclein

    Annals of Neurology

    Volume 64, Issue 3, 28 September 2008, Pages: 348–352, Terhi Peuralinna, Minna Oinas, Tuomo Polvikoski, Anders Paetau, Raimo Sulkava, Leena Niinistö, Hannu Kalimo, Dena Hernandez, John Hardy, Andrew Singleton, Pentti J. Tienari and Liisa Myllykangas

    Version of Record online : 25 JUL 2008, DOI: 10.1002/ana.21446

  8. G51D α-synuclein mutation causes a novel Parkinsonian–pyramidal syndrome

    Annals of Neurology

    Volume 73, Issue 4, April 2013, Pages: 459–471, Suzanne Lesage, Mathieu Anheim, Franck Letournel, Luc Bousset, Aurélie Honoré, Nelly Rozas, Laura Pieri, Karine Madiona, Alexandra Dürr, Ronald Melki, Christophe Verny, Alexis Brice and for the French Parkinson's Disease Genetics Study Group

    Version of Record online : 21 MAY 2013, DOI: 10.1002/ana.23894

  9. Association of SNCA with Parkinson: Replication in the Harvard NeuroDiscovery Center Biomarker Study

    Movement Disorders

    Volume 26, Issue 12, October 2011, Pages: 2283–2286, Hongliu Ding, Alison K. Sarokhan, Sarah S. Roderick, Rachit Bakshi, Nancy E. Maher, Paymon Ashourian, Caroline G. Kan, Sunny Chang, Andrea Santarlasci, Kyleen E. Swords, Bernard M. Ravina, Michael T. Hayes, U. Shivraj Sohur, Anne-Marie Wills, Alice W. Flaherty, Vivek K. Unni, Albert Y. Hung, Dennis J. Selkoe, Michael A. Schwarzschild, Michael G. Schlossmacher, Lewis R. Sudarsky, John H. Growdon, Adrian J. Ivinson, Bradley T. Hyman and Clemens R. Scherzer

    Version of Record online : 23 SEP 2011, DOI: 10.1002/mds.23934

  10. Alpha-synuclein gene duplication: Marked intrafamilial variability in two novel pedigrees

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 813–817, Antonio E. Elia, Simona Petrucci, Alfonso Fasano, Marco Guidi, Stefano Valbonesi, Laura Bernardini, Federica Consoli, Alessandro Ferraris, Alberto Albanese and Enza Maria Valente

    Version of Record online : 6 JUN 2013, DOI: 10.1002/mds.25518

  11. Clinical course of the first Asian family with Parkinsonism related to SNCA triplication

    Movement Disorders

    Volume 25, Issue 16, 15 December 2010, Pages: 2871–2875, Takeshi Sekine, Hajime Kagaya, Manabu Funayama, Yuanzhe Li, Hiroyo Yoshino, Hiroyuki Tomiyama and Nobutaka Hattori

    Version of Record online : 3 SEP 2010, DOI: 10.1002/mds.23313

  12. Motor and Nonmotor Features of Carriers of the p.A53T Alpha-Synuclein Mutation: A Longitudinal Study

    Movement Disorders

    Dimitra Papadimitriou, Roubina Antonelou, Michael Miligkos, Matina Maniati, Nikolaos Papagiannakis, Sevasti Bostantjopoulou, Athannassios Leonardos, Christos Koros, Athina Simitsi, Sokratis G. Papageorgiou, Elisabeth Kapaki, Roy N. Alcalay, Alexandros Papadimitriou, Aglaia Athanassiadou, Maria Stamelou and Leonidas Stefanis

    Version of Record online : 29 MAR 2016, DOI: 10.1002/mds.26615

  13. Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium

    Movement Disorders

    Volume 28, Issue 12, October 2013, Pages: 1740–1744, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Jan O. Aasly, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien, Maria Bozi, Alexis Brice, Laura Brighina, Jonathan Carr, Marie-Christine Chartier-Harlin, Efthimios Dardiotis, Dennis W. Dickson, Nancy N. Diehl, Alexis Elbaz, Carlo Ferrarese, Brian Fiske, J. Mark Gibson, Rachel Gibson, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P.A. Ioannidis, Magdalena Boczarska-Jedynak, Barbara Jasinska-Myga, Beom S. Jeon, Yun Joong Kim, Christine Klein, Rejko Kruger, Elli Kyratzi, Suzanne Lesage, Chin-Hsien Lin, Timothy Lynch, Demetrius M. Maraganore, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Sung Sup Park, Simona Petrucci, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Young Ho Sohn, Leonidas Stefanis, Vera Tadic, Jessie Theuns, Hiroyuki Tomiyama, Ryan J. Uitti, Enza Maria Valente, Christine Van Broeckhoven, Simone van de Loo, Demetrios K. Vassilatis, Carles Vilariño-Güell, Linda R. White, Karin Wirdefeldt, Zbigniew K. Wszolek, Ruey-Meei Wu, Faycal Hentati, Matthew J. Farrer, Owen A. Ross and on behalf of the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium

    Version of Record online : 2 AUG 2013, DOI: 10.1002/mds.25600

  14. A mir-153 binding site variation in SNCA in a patient with Parkinson's disease

    Movement Disorders

    Volume 28, Issue 12, October 2013, Pages: 1755–1756, Han-Joon Kim, Gibeom Park, Beom S. Jeon, Woong Yang Park and Young Eun Kim

    Version of Record online : 14 MAY 2013, DOI: 10.1002/mds.25505

  15. Alpha-synuclein and heroin craving in opiate-dependent patients on injectable heroin maintenance

    Addiction Biology

    Volume 17, Issue 5, September 2012, Pages: 875–886, Kenneth M. Dürsteler-MacFarland, Isabelle Brugger, Dominikus Bönsch, Otto Schmid, Johannes Kornhuber, Stefan Bleich and Gerhard A. Wiesbeck

    Version of Record online : 11 FEB 2011, DOI: 10.1111/j.1369-1600.2010.00293.x

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    Acid β-glucosidase mutants linked to gaucher disease, parkinson disease, and lewy body dementia alter α-synuclein processing

    Annals of Neurology

    Volume 69, Issue 6, June 2011, Pages: 940–953, Valerie Cullen, S. Pablo Sardi, Juliana Ng, You-Hai Xu, Ying Sun, Julianna J. Tomlinson, Piotr Kolodziej, Ilana Kahn, Paul Saftig, John Woulfe, Jean-Christophe Rochet, Marcie A. Glicksman, Seng H. Cheng, Gregory A. Grabowski, Lamya S. Shihabuddin and Michael G. Schlossmacher

    Version of Record online : 6 APR 2011, DOI: 10.1002/ana.22400

  17. Two Parkinson's disease patients with α-synuclein gene duplication and rapid cognitive decline

    Movement Disorders

    Volume 25, Issue 7, 15 May 2010, Pages: 957–959, Chae Won Shin, Hee Jin Kim, Sung Sup Park, Sung Yeun Kim, Ji Yeon Kim and Beom Seok Jeon

    Version of Record online : 10 MAR 2010, DOI: 10.1002/mds.23043

  18. A mutant PSEN1 causes dementia with lewy bodies and variant Alzheimer's disease

    Annals of Neurology

    Volume 57, Issue 3, March 2005, Pages: 429–434, Atsushi Ishikawa, Yue-Shan Piao, Akinori Miyashita, Ryozo Kuwano, Osamu Onodera, Hiroaki Ohtake, Masahiro Suzuki, Masatoyo Nishizawa and Hitoshi Takahashi

    Version of Record online : 24 FEB 2005, DOI: 10.1002/ana.20393

  19. Parkinson's disease correlates with promoter methylation in the α-synuclein gene

    Movement Disorders

    Volume 30, Issue 4, April 2015, Pages: 577–580, Lasse Pihlstrøm, Victoria Berge, Aina Rengmark and Mathias Toft

    Version of Record online : 27 DEC 2014, DOI: 10.1002/mds.26073

  20. The many faces of alpha-synuclein mutations

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 697–701, Meike Kasten and Christine Klein

    Version of Record online : 14 MAY 2013, DOI: 10.1002/mds.25499