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There are 151231 results for: content related to: BDNF Val66Met polymorphism in primary adult-onset dystonia: A case-control study and meta-analysis

  1. 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

  2. Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations

    Movement Disorders

    Volume 28, Issue 14, December 2013, Pages: 1966–1971, Roy N. Alcalay, Anat Mirelman, Rachel Saunders-Pullman, Ming-X Tang, Helen Mejia Santana, Deborah Raymond, Ernest Roos, Martha Orbe-Reilly, Tanya Gurevich, Anat Bar Shira, Mali Gana Weisz, Kira Yasinovsky, Maayan Zalis, Avner Thaler, Andres Deik, Matthew James Barrett, Jose Cabassa, Mark Groves, Ann L. Hunt, Naomi Lubarr, Marta San Luciano, Joan Miravite, Christina Palmese, Rivka Sachdev, Harini Sarva, Lawrence Severt, Vicki Shanker, Matthew Carrington Swan, Jeannie Soto-Valencia, Brooke Johannes, Robert Ortega, Stanley Fahn, Lucien Cote, Cheryl Waters, Pietro Mazzoni, Blair Ford, Elan Louis, Oren Levy, Llency Rosado, Diana Ruiz, Tsvyatko Dorovski, Michael Pauciulo, William Nichols, Avi Orr-Urtreger, Laurie Ozelius, Lorraine Clark, Nir Giladi, Susan Bressman and Karen S. Marder

    Version of Record online : 15 OCT 2013, DOI: 10.1002/mds.25647

  3. Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study

    Movement Disorders

    Volume 29, Issue 14, December 2014, Pages: 1825–1828, Pilar Gómez-Garre, Ismael Huertas-Fernández, María Teresa Cáceres-Redondo, Araceli Alonso-Canovas, Inmaculada Bernal-Bernal, Alberto Blanco-Ollero, Marta Bonilla-Toribio, Juan Andrés Burguera, Manuel Carballo, Fatima Carrillo, M. José Catalán-Alonso, Francisco Escamilla-Sevilla, Raul Espinosa-Rosso, María Carmen Fernández-Moreno, Juan García-Caldentey, José Manuel García-Moreno, Sandra Giacometti-Silveira, Javier Gutiérrez-García, Silvia Jesús-Maestre, Eva López-Valdés, Juan Carlos Martínez-Castrillo, María Pilar Medialdea-Natera, Carolina Méndez-Lucena, Adolfo Mínguez-Castellanos, Miguel Angel Moya, Juan José Ochoa-Sepulveda, Tomas Ojea, Nuria Rodríguez, Ignacio Rubio-Agusti, Miriam Sillero-Sánchez, Javier del Val, Laura Vargas-González and Pablo Mir

    Version of Record online : 25 SEP 2014, DOI: 10.1002/mds.26044

  4. Genome-wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?

    Movement Disorders

    Volume 29, Issue 7, June 2014, Pages: 921–927, Katja Lohmann, Alexander Schmidt, Arne Schillert, Susen Winkler, Alberto Albanese, Frank Baas, Anna Rita Bentivoglio, Friederike Borngräber, Norbert Brüggemann, Giovanni Defazio, Francesca Del Sorbo, Günther Deuschl, Mark J. Edwards, Thomas Gasser, Pilar Gómez-Garre, Julia Graf, Justus L. Groen, Anne Grünewald, Johann Hagenah, Claudia Hemmelmann, Hans-Christian Jabusch, Ryuji Kaji, Meike Kasten, Hideshi Kawakami, Vladimir S. Kostic, Maria Liguori, Pablo Mir, Alexander Münchau, Felicia Ricchiuti, Stefan Schreiber, Katharina Siegesmund, Marina Svetel, Marina A.J. Tijssen, Enza Maria Valente, Ana Westenberger, Kirsten E. Zeuner, Simone Zittel, Eckart Altenmüller, Andreas Ziegler and Christine Klein

    Version of Record online : 26 DEC 2013, DOI: 10.1002/mds.25791

  5. Myoclonus in mitochondrial disorders

    Movement Disorders

    Volume 29, Issue 6, May 2014, Pages: 722–728, Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Michela Catteruccia, Elena Pegoraro, Valerio Carelli, Maria L. Valentino, Giacomo P. Comi, Carlo Minetti, Claudio Bruno, Maurizio Moggio, Elena Caldarazzo Ienco, Tiziana Mongini, Liliana Vercelli, Guido Primiano, Serenella Servidei, Paola Tonin, Mauro Scarpelli, Antonio Toscano, Olimpia Musumeci, Isabella Moroni, Graziella Uziel, Filippo M. Santorelli, Claudia Nesti, Massimiliano Filosto, Costanza Lamperti, Massimo Zeviani and Gabriele Siciliano

    Version of Record online : 7 FEB 2014, DOI: 10.1002/mds.25839

  6. Which ante mortem clinical features predict progressive supranuclear palsy pathology?

    Movement Disorders

    Volume 32, Issue 7, July 2017, Pages: 995–1005, Gesine Respondek, Carolin Kurz, Thomas Arzberger, Yaroslau Compta, Elisabet Englund, Leslie W. Ferguson, Ellen Gelpi, Armin Giese, David J. Irwin, Wassilios G. Meissner, Christer Nilsson, Alexander Pantelyat, Alex Rajput, John C. van Swieten, Claire Troakes, Keith A. Josephs, Anthony E. Lang, Brit Mollenhauer, Ulrich Müller, Jennifer L. Whitwell, Angelo Antonini, Kailash P. Bhatia, Yvette Bordelon, Jean-Christophe Corvol, Carlo Colosimo, Richard Dodel, Murray Grossman, Jan Kassubek, Florian Krismer, Johannes Levin, Stefan Lorenzl, Huw Morris, Peter Nestor, Wolfgang H. Oertel, Gil D. Rabinovici, James B. Rowe, Thilo van Eimeren, Gregor K. Wenning, Adam Boxer, Lawrence I. Golbe, Irene Litvan, Maria Stamelou, Günter U. Höglinger and for the Movement Disorder Society-Endorsed PSP Study Group

    Version of Record online : 13 MAY 2017, DOI: 10.1002/mds.27034

  7. Task force report: Scales for screening and evaluating tremor: Critique and recommendations

    Movement Disorders

    Volume 28, Issue 13, November 2013, Pages: 1793–1800, Rodger Elble, Peter Bain, Maria João Forjaz, Dietrich Haubenberger, Claudia Testa, Christopher G. Goetz, Albert F. G. Leentjens, Pablo Martinez-Martin, Anne Pavy-Le Traon, Bart Post, Cristina Sampaio, Glenn T. Stebbins, Daniel Weintraub and Anette Schrag

    Version of Record online : 3 SEP 2013, DOI: 10.1002/mds.25648

  8. Neuropathy and levodopa in Parkinson's disease: Evidence from a multicenter study

    Movement Disorders

    Volume 28, Issue 10, September 2013, Pages: 1391–1397, Roberto Ceravolo, Giovanni Cossu, Monica Bandettini di Poggio, Lucio Santoro, Paolo Barone, Maurizio Zibetti, Daniela Frosini, Valentina Nicoletti, Fiore Manganelli, Rosa Iodice, Marina Picillo, Aristide Merola, Leonardo Lopiano, Alessandra Paribello, Davide Manca, Maurizio Melis, Roberta Marchese, Paolo Borelli, Alessandra Mereu, Paolo Contu, Giovanni Abbruzzese and Ubaldo Bonuccelli

    Version of Record online : 8 JUL 2013, DOI: 10.1002/mds.25585

  9. The focal dystonias: Current views and challenges for future research

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 926–943, H. A. Jinnah, Alfredo Berardelli, Cynthia Comella, Giovanni DeFazio, Mahlon R. DeLong, Stewart Factor, Wendy R. Galpern, Mark Hallett, Christy L. Ludlow, Joel S. Perlmutter, Ami R. Rosen and for the Dystonia Coalition Investigators

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25567

  10. Disrupted cerebellar connectivity reduces whole-brain network efficiency in multiple system atrophy

    Movement Disorders

    Volume 28, Issue 3, March 2013, Pages: 362–369, Chia-Feng Lu, Bing-Wen Soong, Hsiu-Mei Wu, Shin Teng, Po-Shan Wang and Yu-Te Wu

    Version of Record online : 16 JAN 2013, DOI: 10.1002/mds.25314

  11. The syndrome of deafness-dystonia: Clinical and genetic heterogeneity

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 795–803, Maja Kojovic, Isabel Pareés, Tania Lampreia, Karolina Pienczk-Reclawowicz, Georgia Xiromerisiou, Ignacio Rubio-Agusti, Milica Kramberger, Miryam Carecchio, Anas M. Alazami, Francesco Brancati, Jaroslaw Slawek, Zvezdan Pirtosek, Enza Maria Valente, Fowzan S. Alkuraya, Mark J. Edwards and Kailash P. Bhatia

    Version of Record online : 15 FEB 2013, DOI: 10.1002/mds.25394

  12. Delayed-onset Friedreich's ataxia revisited

    Movement Disorders

    Volume 31, Issue 1, January 2016, Pages: 62–69, Claire Lecocq, Perrine Charles, Jean-Philippe Azulay, Wassilios Meissner, Myriam Rai, Karine N'Guyen, Yann Péréon, Nelly Fabre, Elsa Robin, Sylvie Courtois, Lucie Guyant-Maréchal, Fabien Zagnoli, Gabrielle Rudolf, Mathilde Renaud, Mathieu Sévin-Allouet, Fabien Lesne, Nick Alaerts, Cyril Goizet, Patrick Calvas, Alexandre Eusebio, Claire Guissart, Pascal Derkinderen, Francois Tison, Alexis Brice, Michel Koenig, Massimo Pandolfo, Christine Tranchant, Alexandra Dürr and Mathieu Anheim

    Version of Record online : 21 SEP 2015, DOI: 10.1002/mds.26382

  13. Parkinson's disease patients show reduced cortical-subcortical sensorimotor connectivity

    Movement Disorders

    Volume 28, Issue 4, April 2013, Pages: 447–454, Michael Sharman, Romain Valabregue, Vincent Perlbarg, Linda Marrakchi-Kacem, Marie Vidailhet, Habib Benali, Alexis Brice and Stephane Lehéricy

    Version of Record online : 9 NOV 2012, DOI: 10.1002/mds.25255

  14. Enlarged hyperechogenic substantia nigra as a risk marker for Parkinson's disease

    Movement Disorders

    Volume 28, Issue 2, February 2013, Pages: 216–219, Daniela Berg, Stefanie Behnke, Klaus Seppi, Jana Godau, Stefanie Lerche, Philipp Mahlknecht, Inga Liepelt-Scarfone, Christoph Pausch, Niko Schneider, Alexandra Gaenslen, Kathrin Brockmann, Karin Srulijes, Heiko Huber, Isabel Wurster, Heike Stockner, Stefan Kiechl, Johann Willeit, Arno Gasperi, Klaus Fassbender, Thomas Gasser and Werner Poewe

    Version of Record online : 31 OCT 2012, DOI: 10.1002/mds.25192

  15. You have full text access to this OnlineOpen article
    The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease

    Movement Disorders

    Volume 28, Issue 2, February 2013, Pages: 232–236, Raquel Duran, Niccolo E. Mencacci, Aikaterini V. Angeli, Maryam Shoai, Emma Deas, Henry Houlden, Atul Mehta, Derralynn Hughes, Timothy M. Cox, Patrick Deegan, Anthony H. Schapira, Andrew J. Lees, Patricia Limousin, Paul R. Jarman, Kailash P. Bhatia, Nicholas W. Wood, John Hardy and Tom Foltynie

    Version of Record online : 5 DEC 2012, DOI: 10.1002/mds.25248

  16. Action inhibition in Tourette syndrome

    Movement Disorders

    Volume 29, Issue 12, October 2014, Pages: 1532–1538, Christos Ganos, Simone Kühn, Ursula Kahl, Odette Schunke, Jan Feldheim, Christian Gerloff, Veit Roessner, Tobias Bäumer, Götz Thomalla, Patrick Haggard and Alexander Münchau

    Version of Record online : 3 JUL 2014, DOI: 10.1002/mds.25944

  17. 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

  18. High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometry

    Movement Disorders

    Volume 30, Issue 8, July 2015, Pages: 1077–1084, Nadya Pyatigorskaya, Michael Sharman, Jean-Christophe Corvol, Romain Valabregue, Lydia Yahia-Cherif, Fabrice Poupon, Florence Cormier-Dequaire, Hartwig Siebner, Stephan Klebe, Marie Vidailhet, Alexis Brice and Stephane Lehéricy

    Version of Record online : 22 MAY 2015, DOI: 10.1002/mds.26218

  19. The clinical spectrum of anxiety in Parkinson's disease

    Movement Disorders

    Volume 29, Issue 8, July 2014, Pages: 967–975, Nadeeka N.N.W. Dissanayaka, Elizabeth White, John D. O'Sullivan, Rodney Marsh, Nancy A. Pachana and Gerard J. Byrne

    Version of Record online : 17 JUL 2014, DOI: 10.1002/mds.25937

  20. In vivo gastric detection of α-synuclein inclusions in Parkinson's disease

    Movement Disorders

    Volume 30, Issue 4, April 2015, Pages: 517–524, Álvaro Sánchez-Ferro, Alberto Rábano, María José Catalán, Fernando Canga Rodríguez-Valcárcel, Servando Fernández Díez, Jaime Herreros-Rodríguez, Elvira García-Cobos, Marina Mata Álvarez-Santullano, Lydia López-Manzanares, Antonio J. Mosqueira, Lydia Vela Desojo, Juan José López-Lozano, Eva López-Valdés, Rafael Sánchez-Sánchez and José Antonio Molina-Arjona

    Version of Record online : 11 AUG 2014, DOI: 10.1002/mds.25988