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There are 9382 results for: content related to: Dramatic response of facial stereotype/tic to tetrabenazine in the first reported cases of neuroferritinopathy in the United States

  1. A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations

    Movement Disorders

    Volume 24, Issue 3, 15 February 2009, Pages: 441–445, Akatsuki Kubota, Ayumi Hida, Yaeko Ichikawa, Yoshio Momose, Jun Goto, Yukifusa Igeta, Hideji Hashida, Kunihiro Yoshida, Syu-Ichi Ikeda, Ichiro Kanazawa and Shoji Tsuji

    Version of Record online : 31 DEC 2008, DOI: 10.1002/mds.22435

  2. 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

  3. Adult-onset generalized dystonia due to a mutation in the neuroferritinopathy gene

    Movement Disorders

    Volume 20, Issue 2, February 2005, Pages: 243–245, Pablo Mir, Mark J. Edwards, Andrew R.J. Curtis, Kailash P. Bhatia and Niall P. Quinn

    Version of Record online : 18 AUG 2004, DOI: 10.1002/mds.20280

  4. Spectrum of movement disorders in neuroferritinopathy

    Movement Disorders

    Volume 20, Issue 1, January 2005, Pages: 95–99, Douglas E. Crompton, Patrick F. Chinnery, David Bates, Timothy J. Walls, Margaret J. Jackson, Andrew J. Curtis and John Burn

    Version of Record online : 18 AUG 2004, DOI: 10.1002/mds.20284

  5. Huntington's disease phenocopies are clinically and genetically heterogeneous

    Movement Disorders

    Volume 23, Issue 5, 15 April 2008, Pages: 716–720, Edward J. Wild, Ese E. Mudanohwo, Mary G. Sweeney, Susanne A. Schneider, Jon Beck, Kailash P. Bhatia, Martin N. Rossor, Mary B. Davis and Sarah J. Tabrizi

    Version of Record online : 7 JAN 2008, DOI: 10.1002/mds.21915

  6. Early neuropsychiatry features in neuroferritinopathy

    Movement Disorders

    Volume 28, Issue 9, August 2013, Pages: 1310–1313, Michael J. Keogh, Baldev Singh and Patrick F. Chinnery

    Version of Record online : 23 FEB 2013, DOI: 10.1002/mds.25371

  7. Huntington disease and Huntington disease-like in a case series from Brazil

    Clinical Genetics

    Volume 86, Issue 4, October 2014, Pages: 373–377, R.M. Castilhos, A.F.D. Souza, G.V. Furtado, T.C. Gheno, A.L. Silva, F.R. Vargas, M.-A.F.D. Lima, O. Barsottini, J.L. Pedroso, C. Godeiro Jr, D. Salarini, E.T. Pereira, K. Lin, M.-B. Toralles, J.A.M. Saute, C.R. Rieder, M. Quintas, J. Sequeiros, I. Alonso, M.L. Saraiva-Pereira and L.B. Jardim

    Version of Record online : 17 OCT 2013, DOI: 10.1111/cge.12283

  8. Neurodegeneration with Brain Iron Accumulation: Clinicoradiological Approach to Diagnosis

    Journal of Neuroimaging

    Volume 25, Issue 4, July/August 2015, Pages: 539–551, Lázaro L. F. Amaral, Santhosh Gaddikeri, Philip R. Chapman, Rasmoni Roy, Ramya S. Gaddikeri, Victor Hugo Marussi and Asim K. Bag

    Version of Record online : 24 DEC 2014, DOI: 10.1111/jon.12195

  9. Abnormalities of the nucleus and nuclear inclusions in neurodegenerative disease: a work in progress

    Neuropathology and Applied Neurobiology

    Volume 33, Issue 1, February 2007, Pages: 2–42, J. M. Woulfe

    Version of Record online : 12 JAN 2007, DOI: 10.1111/j.1365-2990.2006.00819.x

  10. Neurodegeneration with Brain Iron Accumulation, Wilson Disease, and Manganism

    Neurodegeneration

    Anthony Schapira, Zbigniew Wszolek, Ted M. Dawson, Nicholas Wood, Pages: 317–326, 2017

    Published Online : 18 FEB 2017, DOI: 10.1002/9781118661895.ch26

  11. A unique case of cortical myoclonus sensitive to visual stimuli in the peripersonal space

    Movement Disorders

    Volume 24, Issue 3, 15 February 2009, Pages: 422–425, Sharavanan Parasivam, Max Cowey, Bruce Day and Dominic Thyagarajan

    Version of Record online : 15 DEC 2008, DOI: 10.1002/mds.21931

  12. Hereditary Ferritinopathies

    Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders, Second Edition

    Ruben Vidal, Marie Bernadette Delisle, Olivier Rascol, Bernardino Ghetti, Pages: 461–466, 2011

    Published Online : 21 SEP 2011, DOI: 10.1002/9781444341256.ch49

  13. The man who could not walk backward: An unusual presentation of neuroferritinopathy

    Movement Disorders

    Volume 26, Issue 2, 1 February 2011, Pages: 362–364, Adam J. Cassidy, Elizabeth R. Williams, Paul Goldsmith, Stuart N. Baker and Mark R. Baker

    Version of Record online : 3 FEB 2011, DOI: 10.1002/mds.23415

  14. Susceptibility weighted imaging: A pictorial review

    Journal of Medical Imaging and Radiation Oncology

    Volume 54, Issue 5, October 2010, Pages: 435–449, Benjamin C Ong and Stephen L Stuckey

    Version of Record online : 20 OCT 2010, DOI: 10.1111/j.1754-9485.2010.02208.x

  15. Neurodegeneration With Brain Iron Accumulation (NBIA) Syndromes Presenting With Late-Onset Craniocervical Dystonia: An Illustrative Case Series‎

    Movement Disorders Clinical Practice

    Volume 4, Issue 2, March/April 2017, Pages: 254–257, Florian Brugger, Georg Kägi, Massimo Pandolfo, Niccolò E. Mencacci, Amit Batla, Sarah Wiethoff and Kailash P. Bhatia

    Version of Record online : 18 JUL 2016, DOI: 10.1002/mdc3.12393

  16. Neurodegeneration: iron weighs in

    Clinical Genetics

    Volume 60, Issue 4, October 2001, Pages: 267–269, D Elterman, S Warby and BA Coburn

    Version of Record online : 12 JAN 2002, DOI: 10.1034/j.1399-0004.2001.600403.3.x

  17. You have free access to this content
    Erratum to: 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 6, May 2012, Page: 809,

    Version of Record online : 30 MAR 2012, DOI: 10.1002/mds.24972

  18. Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)

    Movement Disorders

    Volume 24, Issue 11, 15 August 2009, Pages: 1676–1683, Fabienne Ory-Magne, Christine Brefel-Courbon, Pierre Payoux, Sabrina Debruxelles, Igor Sibon, Cyril Goizet, Pierre Labauge, Patrice Menegon, Emmanuelle Uro-Coste, Bernardino Ghetti, Marie Bernadetle Delisle, Ruben Vidal and Olivier Rascol

    Version of Record online : 9 JUN 2009, DOI: 10.1002/mds.22669

  19. Secondary Dystonias

    Hyperkinetic Movement Disorders: Differential Diagnosis and Treatment

    Alberto Albanese, Joseph Jankovic, Pages: 135–145, 2012

    Published Online : 24 FEB 2012, DOI: 10.1002/9781444346183.ch9

  20. 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