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There are 40453 results for: content related to: Imaging striatal dopaminergic function in Phospholipase A2 Group VI –related parkinsonism

  1. Novel mutations in siblings with later-onset PLA2G6-associated neurodegeneration (PLAN)

    Movement Disorders

    Volume 26, Issue 9, 1 August 2011, Pages: 1766–1767, Matthew A. Bower, Khalaf Bushara, Melissa A. Dempsey, Soma Das and Paul J. Tuite

    Version of Record online : 25 APR 2011, DOI: 10.1002/mds.23617

  2. PLA2G6 mutations and Parkinson's disease

    Annals of Neurology

    Volume 67, Issue 1, January 2010, Pages: 147–148, E. K. Tan, P. Ho, L. Tan, K. M. Prakash and Y. Zhao

    Version of Record online : 20 MAR 2009, DOI: 10.1002/ana.21663

  3. First video report of static encephalopathy of childhood with neurodegeneration in adulthood

    Movement Disorders

    Volume 28, Issue 3, March 2013, Pages: 397–399, Emi Kasai-Yoshida, Satoko Kumada, Akira Yagishita, Konomi Shimoda, Ikuko Sato-Shirai, Yasuo Hachiya and Eiji Kurihara

    Version of Record online : 6 FEB 2013, DOI: 10.1002/mds.25158

  4. Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration

    Movement Disorders

    Volume 29, Issue 4, April 2014, Pages: 574–575, Geetanjali S. Rathore, Christian P. Schaaf and Amber J. Stocco

    Version of Record online : 7 MAR 2014, DOI: 10.1002/mds.25868

  5. Early onset dystonia and parkinsonism with abnormal globus pallidal signal in MRI: A diagnostic challenge

    Movement Disorders

    Volume 28, Issue 14, December 2013, Pages: 2035–2036, Bart Post, Martine van Belzen, Carlo Marcelis, Frederick J. A. Meijer, Michel A. Willemsen and Bart P. van de Warrenburg

    Version of Record online : 3 SEP 2013, DOI: 10.1002/mds.25622

  6. Twin-sisters with PLA2G6-associated neurodegeneration due to paternal isodisomy of the chromosome 22 following in vitro fertilization

    Clinical Genetics

    Volume 92, Issue 1, July 2017, Pages: 117–118, C. Tello, A. Darling, V. Lupo, C.I. Ortez, B. Pérez-Dueñas and C. Espinós

    Version of Record online : 1 FEB 2017, DOI: 10.1111/cge.12925

  7. Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration

    European Journal of Neurology

    Volume 23, Issue 4, April 2016, Pages: e24–e25, I. Kraoua, M. Romani, D. Tonduti, H. BenRhouma, G. Zorzi, F. Zibordi, A. Ardissone, N. Gouider-Khouja, I. Ben Youssef-Turki, N. Nardocci and E. M. Valente

    Version of Record online : 18 MAR 2016, DOI: 10.1111/ene.12927

  8. 1984–2014. Normal Accidents. Was Charles Perrow Right for the Wrong Reasons?

    Journal of Contingencies and Crisis Management

    Volume 23, Issue 4, December 2015, Pages: 275–286, Jean-Christophe Le Coze

    Version of Record online : 26 JUN 2015, DOI: 10.1111/1468-5973.12090

  9. Novel splice-site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophy

    Clinical Genetics

    Volume 78, Issue 5, November 2010, Pages: 432–440, A Tonelli, R Romaniello, R Grasso, A Cavallini, A Righini, N Bresolin, R Borgatti and MT Bassi

    Version of Record online : 27 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01417.x

  10. PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 2, March 2012, Pages: 183–191, Chin-Song Lu, Szu-Chia Lai, Ruey-Meei Wu, Yi-Hsin Weng, Chia-Ling Huang, Rou-Shayn Chen, Hsiu-Chen Chang, Yah-Huei Wu-Chou and Tu-Hsueh Yeh

    Version of Record online : 27 DEC 2011, DOI: 10.1002/ajmg.b.32012

  11. You have free access to this content
    Neuroaxonal dystrophy in PLA2G6 knockout mice


    Volume 35, Issue 3, June 2015, Pages: 289–302, Hisae Sumi-Akamaru, Goichi Beck, Shinsuke Kato and Hideki Mochizuki

    Version of Record online : 6 MAY 2015, DOI: 10.1111/neup.12202

  12. Marked diurnal fluctuation and rest benefit in a patient with parkin mutation

    Movement Disorders

    Volume 23, Issue 4, 15 March 2008, Pages: 624–626, Sun J. Chung, Hee K. Park, Chang-Seok Ki, Mi J. Kim and Myoung C. Lee

    Version of Record online : 28 JAN 2008, DOI: 10.1002/mds.21951

  13. A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 290–292, G. Schottmann, W. Stenzel, S. Lützkendorf, M. Schuelke and E. Knierim

    Version of Record online : 25 MAR 2013, DOI: 10.1111/cge.12137

  14. Response to: ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation

    Movement Disorders

    Volume 25, Issue 13, 15 October 2010, Page: 2253, Alisdair McNeill

    Version of Record online : 24 AUG 2010, DOI: 10.1002/mds.23224

  15. You have full text access to this OnlineOpen article
    Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories

    Neuropathology and Applied Neurobiology

    Volume 42, Issue 3, April 2016, Pages: 220–241, C. E. Arber, A. Li, H. Houlden and S. Wray

    Version of Record online : 2 JUN 2015, DOI: 10.1111/nan.12242

  16. Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations

    Movement Disorders

    Volume 27, Issue 1, January 2012, Pages: 42–53, Susanne A. Schneider, John Hardy and Kailash P. Bhatia

    Version of Record online : 26 OCT 2011, DOI: 10.1002/mds.23971

  17. PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

    Clinical Genetics

    B. Ozes, N. Karagoz, R. Schüle, A. Rebelo, M.-J. Sobrido, F. Harmuth, M. Synofzik, S.I.P. Pascual, M. Colak, B. Ciftci-Kavaklioglu, B. Kara, A. Ordóñez-Ugalde, B. Quintáns, M.A. Gonzalez, A. Soysal, S. Zuchner and E. Battaloglu

    Version of Record online : 19 APR 2017, DOI: 10.1111/cge.13008

  18. No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia

    Movement Disorders

    Volume 26, Issue 11, September 2011, Pages: 2136–2137, Christoph Kamm, Nils Uflacker, Friedrich Asmus, Christoph Schrader, Alexander Wolters, Matthias Wittstock, Jens Pahnke, Thomas Gasser, Jens Volkmann, Alexander Münchau, Johann Hagenah, Reiner Benecke, Christine Klein and Katja Lohmann

    Version of Record online : 2 JUN 2011, DOI: 10.1002/mds.23777

  19. Deep Brain Stimulation of the Internal Globus Pallidus for Generalized Dystonia Associated with Spinocerebellar Ataxia Type 1: A Case Report

    Neuromodulation: Technology at the Neural Interface

    Volume 17, Issue 4, June 2014, Pages: 389–392, Brian J. Copeland, Albert Fenoy, Timothy M. Ellmore, Qinghua Liang, Vicki Ephron and Mya Schiess

    Version of Record online : 1 JUL 2013, DOI: 10.1111/ner.12081

  20. Learning for progression and employability or learning for learning's sake?

    British Journal of Learning Disabilities

    Volume 41, Issue 4, December 2013, Pages: 249–255, Keith A. Stonier

    Version of Record online : 28 OCT 2013, DOI: 10.1111/bld.12049