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There are 2610 results for: content related to: Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond

  1. You have free access to this content
    Poster Session

    Movement Disorders

    Volume 31, Issue S2, June 2016, Pages: S1–S697,

    Version of Record online : 19 JUN 2016, DOI: 10.1002/mds.26688

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    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

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    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

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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

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    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Version of Record online : 6 JUN 2014, DOI: 10.1002/mds.25914

  6. Glucocerebrosidase mutations and neuropsychiatric phenotypes in Parkinson's disease and Lewy body dementias: Review and meta-analyses

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Byron Creese, Emily Bell, Iskandar Johar, Paul Francis, Clive Ballard and Dag Aarsland

    Version of Record online : 26 MAY 2017, DOI: 10.1002/ajmg.b.32549

  7. You have full text access to this OnlineOpen article
    Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

    Annals of Neurology

    Volume 80, Issue 5, November 2016, Pages: 674–685, Ganqiang Liu, Brendon Boot, Joseph J. Locascio, Iris E. Jansen, Sophie Winder-Rhodes, Shirley Eberly, Alexis Elbaz, Alexis Brice, Bernard Ravina, Jacobus J. van Hilten, Florence Cormier-Dequaire, Jean-Christophe Corvol, Roger A. Barker, Peter Heutink, Johan Marinus, Caroline H. Williams-Gray, Clemens R. Scherzer and for the International Genetics of Parkinson Disease Progression (IGPP) Consortium

    Version of Record online : 18 NOV 2016, DOI: 10.1002/ana.24781

  8. Survival and dementia in GBA-associated Parkinson's disease: The mutation matters

    Annals of Neurology

    Volume 80, Issue 5, November 2016, Pages: 662–673, Roberto Cilia, Sara Tunesi, Giorgio Marotta, Emanuele Cereda, Chiara Siri, Silvana Tesei, Anna L. Zecchinelli, Margherita Canesi, Claudio B. Mariani, Nicoletta Meucci, Giorgio Sacilotto, Michela Zini, Michela Barichella, Corrado Magnani, Stefano Duga, Rosanna Asselta, Giulia Soldà, Agostino Seresini, Manuela Seia, Gianni Pezzoli and Stefano Goldwurm

    Version of Record online : 3 OCT 2016, DOI: 10.1002/ana.24777

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    Glucocerebrosidase Mutations alter the endoplasmic reticulum and lysosomes in Lewy body disease

    Journal of Neurochemistry

    Volume 123, Issue 2, October 2012, Pages: 298–309, Marzena Kurzawa-Akanbi, Peter S Hanson, Peter G Blain, Debra J Lett, Ian G McKeith, Patrick F Chinnery and Christopher M Morris

    Version of Record online : 22 AUG 2012, DOI: 10.1111/j.1471-4159.2012.07879.x

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    Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains

    Annals of Neurology

    Volume 72, Issue 3, September 2012, Pages: 455–463, Matthew E. Gegg, Derek Burke, Simon J. R. Heales, J. Mark Cooper, John Hardy, Nicholas W. Wood and Anthony H. V. Schapira

    Version of Record online : 2 OCT 2012, DOI: 10.1002/ana.23614

  11. New Directions in Gaucher Disease

    Human Mutation

    Volume 37, Issue 11, November 2016, Pages: 1121–1136, Mia Horowitz, Deborah Elstein, Ari Zimran and Ozlem Goker-Alpan

    Version of Record online : 21 AUG 2016, DOI: 10.1002/humu.23056

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    Variants associated with Gaucher disease in multiple system atrophy

    Annals of Clinical and Translational Neurology

    Volume 2, Issue 4, April 2015, Pages: 417–426, Jun Mitsui, Takashi Matsukawa, Hidenao Sasaki, Ichiro Yabe, Masaaki Matsushima, Alexandra Dürr, Alexis Brice, Hiroshi Takashima, Akio Kikuchi, Masashi Aoki, Hiroyuki Ishiura, Tsutomu Yasuda, Hidetoshi Date, Budrul Ahsan, Atsushi Iwata, Jun Goto, Yaeko Ichikawa, Yasuo Nakahara, Yoshio Momose, Yuji Takahashi, Kenju Hara, Akiyoshi Kakita, Mitsunori Yamada, Hitoshi Takahashi, Osamu Onodera, Masatoyo Nishizawa, Hirohisa Watanabe, Mizuki Ito, Gen Sobue, Kinya Ishikawa, Hidehiro Mizusawa, Kazuaki Kanai, Takamichi Hattori, Satoshi Kuwabara, Kimihito Arai, Shigeru Koyano, Yoshiyuki Kuroiwa, Kazuko Hasegawa, Tatsuhiko Yuasa, Kenichi Yasui, Kenji Nakashima, Hijiri Ito, Yuishin Izumi, Ryuji Kaji, Takeo Kato, Susumu Kusunoki, Yasushi Osaki, Masahiro Horiuchi, Tomoyoshi Kondo, Shigeo Murayama, Nobutaka Hattori, Mitsutoshi Yamamoto, Miho Murata, Wataru Satake, Tatsushi Toda, Alessandro Filla, Thomas Klockgether, Ullrich Wüllner, Garth Nicholson, Sid Gilman, Caroline M. Tanner, Walter A. Kukull, Mathew B. Stern, Virginia M.-Y. Lee, John Q. Trojanowski, Eliezer Masliah, Phillip A. Low, Paola Sandroni, Laurie J. Ozelius, Tatiana Foroud and Shoji Tsuji

    Version of Record online : 28 FEB 2015, DOI: 10.1002/acn3.185

  13. The neuropathology of genetic Parkinson's disease

    Movement Disorders

    Volume 27, Issue 7, June 2012, Pages: 831–842, Markos Poulopoulos, Oren A. Levy and Roy N. Alcalay

    Version of Record online : 26 MAR 2012, DOI: 10.1002/mds.24962

  14. You have full text access to this OnlineOpen article
    GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

    Annals of Clinical and Translational Neurology

    Volume 2, Issue 9, September 2015, Pages: 941–945, Ziv Gan-Or, Anat Mirelman, Ronald B. Postuma, Isabelle Arnulf, Anat Bar-Shira, Yves Dauvilliers, Alex Desautels, Jean-François Gagnon, Claire S. Leblond, Birgit Frauscher, Roy N. Alcalay, Rachel Saunders-Pullman, Susan B. Bressman, Karen Marder, Christelle Monaca, Birgit Högl, Avi Orr-Urtreger, Patrick A. Dion, Jacques Y. Montplaisir, Nir Giladi and Guy A. Rouleau

    Version of Record online : 31 JUL 2015, DOI: 10.1002/acn3.228

  15. Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course

    Movement Disorders

    Volume 27, Issue 3, March 2012, Pages: 393–399, Núria Setó-Salvia, Javier Pagonabarraga, Henry Houlden, Berta Pascual-Sedano, Oriol Dols-Icardo, Arianna Tucci, Coro Paisán-Ruiz, Antonia Campolongo, Sofía Antón-Aguirre, Inés Martín, Laia Muñoz, Enric Bufill, Lluïsa Vilageliu, Daniel Grinberg, Mónica Cozar, Rafael Blesa, Alberto Lleó, John Hardy, Jaime Kulisevsky and Jordi Clarimón

    Version of Record online : 15 DEC 2011, DOI: 10.1002/mds.24045

  16. The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism

    Movement Disorders

    Volume 24, Issue 11, 15 August 2009, Pages: 1571–1578, John DePaolo, Ozlem Goker-Alpan, Ted Samaddar, Grisel Lopez and Ellen Sidransky

    Version of Record online : 7 MAY 2009, DOI: 10.1002/mds.22538

  17. GBA-associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study

    Movement Disorders

    Volume 30, Issue 3, March 2015, Pages: 407–411, Kathrin Brockmann, Karin Srulijes, Sylvia Pflederer, Ann-Kathrin Hauser, Claudia Schulte, Walter Maetzler, Thomas Gasser and Daniela Berg

    Version of Record online : 1 DEC 2014, DOI: 10.1002/mds.26071

  18. Functional brain imaging in glucocerebrosidase mutation carriers with and without Parkinsonism

    Movement Disorders

    Volume 25, Issue 12, 15 September 2010, Pages: 1823–1829, Satoshi Kono, Yasuomi Ouchi, Tatsuhiro Terada, Hiroyuki Ida, Makiko Suzuki and Hiroaki Miyajima

    Version of Record online : 28 JUL 2010, DOI: 10.1002/mds.23213

  19. Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy

    Movement Disorders

    Volume 23, Issue 3, 15 February 2008, Pages: 460–463, Elvira V. De Marco, Grazia Annesi, Patrizia Tarantino, Francesca E. Rocca, Giovanni Provenzano, Donatella Civitelli, Innocenza C. Cirò Candiano, Ferdinanda Annesi, Sara Carrideo, Francesca Condino, Giuseppe Nicoletti, Demetrio Messina, Fabiana Novellino, Maurizio Morelli and Aldo Quattrone

    Version of Record online : 11 DEC 2007, DOI: 10.1002/mds.21892

  20. Genetic assessment of familial and early-onset Parkinson's disease in a Greek population

    European Journal of Neurology

    Volume 21, Issue 7, July 2014, Pages: 963–968, M. Bozi, D. Papadimitriou, R. Antonellou, M. Moraitou, M. Maniati, D. K. Vassilatis, S. G. Papageorgiou, A. Leonardos, G. Tagaris, G. Malamis, D. Theofilopoulos, S. Kamakari, E. Stamboulis, G. M. Hadjigeorgiou, A. Athanassiadou, H. Michelakakis, A. Papadimitriou, T. Gasser and L. Stefanis

    Version of Record online : 7 DEC 2013, DOI: 10.1111/ene.12315