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There are 1267 results for: content related to: PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease

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

    Neuropathology

    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

  2. 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

  3. Follow-up study of 25 Chinese children with PLA2G6-associated neurodegeneration

    European Journal of Neurology

    Volume 20, Issue 2, February 2013, Pages: 322–330, P. Zhang, Z. Gao, Y. Jiang, J. Wang, F. Zhang, S. Wang, Y. Yang, H. Xiong, Y. Zhang, X. Bao, J. Xiao, X. Wu and Y. Wu

    Version of Record online : 31 AUG 2012, DOI: 10.1111/j.1468-1331.2012.03856.x

  4. Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort

    European Journal of Neurology

    Volume 22, Issue 1, January 2015, Pages: 178–186, M. Romani, I. Kraoua, A. Micalizzi, H. Klaa, H. Benrhouma, C. Drissi, I. Turki, S. Castellana, T. Mazza, E. M. Valente and N. Gouider-Khouja

    Version of Record online : 27 AUG 2014, DOI: 10.1111/ene.12552

  5. Clinical study and PLA2G6 mutation screening analysis in Chinese patients with infantile neuroaxonal dystrophy

    European Journal of Neurology

    Volume 16, Issue 2, February 2009, Pages: 240–245, Y. Wu, Y. Jiang, Z. Gao, J. Wang, Y. Yuan, H. Xiong, X. Chang, X. Bao, Y. Zhang, J. Xiao and X. Wu

    Version of Record online : 9 DEC 2008, DOI: 10.1111/j.1468-1331.2008.02397.x

  6. R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family

    European Journal of Neurology

    Volume 16, Issue 1, January 2009, Pages: 101–104, F. Sina, S. Shojaee, E. Elahi and C. Paisán-Ruiz

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1468-1331.2008.02356.x

  7. Genetic variants of PLA2G6 are associated with Type 2 diabetes mellitus and triglyceride levels in a Chinese population

    Diabetic Medicine

    Volume 32, Issue 2, February 2015, Pages: 280–286, J. Yan, C. Hu, F. Jiang, R. Zhang, J. Wang, S. Tang, D. Peng, M. Chen, Y. Bao and W. Jia

    Version of Record online : 10 OCT 2014, DOI: 10.1111/dme.12587

  8. Characterization of PLA2G6 as a locus for dystonia-parkinsonism

    Annals of Neurology

    Volume 65, Issue 1, January 2009, Pages: 19–23, Coro Paisan-Ruiz, Kailash P. Bhatia, Abi Li, Dena Hernandez, Mary Davis, Nick W. Wood, John Hardy, Henry Houlden, Andrew Singleton and Susanne A. Schneider

    Version of Record online : 20 JUN 2008, DOI: 10.1002/ana.21415

  9. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

    Movement Disorders

    Volume 25, Issue 12, 15 September 2010, Pages: 1791–1800, Coro Paisán-Ruiz, Rocio Guevara, Monica Federoff, Hasmet Hanagasi, Fardaz Sina, Elahe Elahi, Susanne A. Schneider, Petra Schwingenschuh, Nin Bajaj, Murat Emre, Andrew B. Singleton, John Hardy, Kailash P. Bhatia, Sebastian Brandner, Andrew J. Lees and Henry Houlden

    Version of Record online : 28 JUL 2010, DOI: 10.1002/mds.23221

  10. 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

  11. 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

  12. Ovarian Steroid Regulation of Endometrial Phospholipase A2 Isoforms in Horses

    Reproduction in Domestic Animals

    Volume 48, Issue 2, April 2013, Pages: 311–316, MM Ababneh and MHT Troedsson

    Version of Record online : 9 AUG 2012, DOI: 10.1111/j.1439-0531.2012.02151.x

  13. You have free access to this content
    Infantile neuroaxonal dystrophy caused by uniparental disomy

    Developmental Medicine & Child Neurology

    Volume 56, Issue 4, April 2014, Pages: 386–389, Joyce Solomons, Oliver Ridgway, Carol Hardy, Manju Kurian, Sandeep Jayawant, Sarah Hughes, Pieter Pretorius and Andrea H Németh

    Version of Record online : 15 NOV 2013, DOI: 10.1111/dmcn.12327

    Corrected by:

    Erratum: Erratum

    Vol. 56, Issue 7, 698, Version of Record online: 12 JUN 2014

  14. 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

  15. Complicated recessive dystonia parkinsonism syndromes

    Movement Disorders

    Volume 24, Issue 4, 15 March 2009, Pages: 490–499, Susanne A. Schneider, Kailash P. Bhatia and John Hardy

    Version of Record online : 30 JAN 2009, DOI: 10.1002/mds.22314

  16. The PLA2G6 gene in early-onset Parkinson's disease

    Movement Disorders

    Volume 26, Issue 13, November 2011, Pages: 2415–2417, Kai Michael Kauther, Christine Höft, Ida Rissling, Wolfgang H. Oertel and Jens Carsten Möller

    Version of Record online : 2 AUG 2011, DOI: 10.1002/mds.23851

  17. Imaging striatal dopaminergic function in Phospholipase A2 Group VI–related parkinsonism

    Movement Disorders

    Volume 27, Issue 13, November 2012, Pages: 1698–1699, Pankaj Agarwal, Penelope Hogarth, Susan Hayflick, Patrick MacLeod, Renju Kuriakose, Jessamyn McKenzie, Nicole Heffernan, Katie Dinelle, Vesna Sossi and A. Jon Stoessl

    Version of Record online : 28 NOV 2012, DOI: 10.1002/mds.25160

  18. You have full text access to this OnlineOpen article
    Pantothenate kinase-associated neurodegeneration is not a synucleinopathy

    Neuropathology and Applied Neurobiology

    Volume 39, Issue 2, February 2013, Pages: 121–131, A. Li, R. Paudel, R. Johnson, R. Courtney, A. J. Lees, J. L. Holton, J. Hardy, T. Revesz and H. Houlden

    Version of Record online : 25 JAN 2013, DOI: 10.1111/j.1365-2990.2012.01269.x

  19. 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

  20. You have free access to this content
    Childhood disorders of neurodegeneration with brain iron accumulation (NBIA)

    Developmental Medicine & Child Neurology

    Volume 53, Issue 5, May 2011, Pages: 394–404, MANJU A KURIAN, ALASDAIR MCNEILL, JEAN-PIERRE LIN and EAMONN R MAHER

    Version of Record online : 12 APR 2011, DOI: 10.1111/j.1469-8749.2011.03955.x