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There are 26581 results for: content related to: Complicated recessive dystonia parkinsonism syndromes

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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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    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

  4. 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

  5. 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

  6. 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

  7. 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

  8. Abstracts

    Movement Disorders

    Volume 31, Issue S1, March 2016, Pages: S12–S100,

    Version of Record online : 10 MAR 2016, DOI: 10.1002/mds.26576

  9. 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

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    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

  11. 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

  12. 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

  13. You have full text access to this OnlineOpen article
    Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes?

    Movement Disorders

    Volume 28, Issue 10, September 2013, Pages: 1325–1329, Maria Stamelou, Scarlett C. Lai, Annu Aggarwal, Susanne A. Schneider, Henry Houlden, Tu-Hsueh Yeh, Amit Batla, Chin-Song Lu, Mohit Bhatt and Kailash P. Bhatia

    Version of Record online : 4 JUN 2013, DOI: 10.1002/mds.25490

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    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

  15. Indian-subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms

    Movement Disorders

    Volume 25, Issue 10, 30 July 2010, Pages: 1424–1431, Annu Aggarwal, Susanne A. Schneider, Henry Houlden, Monty Silverdale, Reema Paudel, Coro Paisan-Ruiz, Shrinivas Desai, Mihir Munshi, Darshana Sanghvi, John Hardy, Kailash P. Bhatia and Mohit Bhatt

    Version of Record online : 1 APR 2010, DOI: 10.1002/mds.23095

  16. Secondary dystonia – clinical clues and syndromic associations

    European Journal of Neurology

    Volume 17, Issue s1, July 2010, Pages: 52–57, S. A. Schneider and K. P. Bhatia

    Version of Record online : 8 JUN 2010, DOI: 10.1111/j.1468-1331.2010.03051.x

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    Atypical PLA2G6-Associated Neurodegeneration: Social Communication Impairment, Dystonia and Response to Deep Brain Stimulation

    Movement Disorders Clinical Practice

    Volume 1, Issue 2, June 2014, Pages: 128–131, Laura Cif, Manju A. Kurian, Victoria Gonzalez, Sara Garcia-Ptacek, Thomas Roujeau, Philippe Gelisse, Ana Maria Moura de Ribeiro, Arielle Crespel, Lesley MacPherson and Philippe Coubes

    Version of Record online : 23 MAY 2014, DOI: 10.1002/mdc3.12030

  18. 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

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    List of Abstracts

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S524–S592,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25052

  20. 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