SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Paola Giunti, Elide Mantuano, Marina Frontali, Liana Veneziano, Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation, Frontiers in Cellular Neuroscience, 2015, 9,

    CrossRef

  2. 2
    Monica Federoff, Lucia V. Schottlaender, Henry Houlden, Andrew Singleton, Multiple system atrophy: the application of genetics in understanding etiology, Clinical Autonomic Research, 2015,

    CrossRef

  3. 3
    Stephen M. Maricich, Huda Y. Zoghbi, Neuromuscular Disorders of Infancy, Childhood, and Adolescence, 2015,

    CrossRef

  4. You have free access to this content4
    Una-Marie Sheerin, Henry Houlden, Nicholas W. Wood, Advances in the Genetics of Parkinson's Disease: A Guide for the Clinician, Movement Disorders Clinical Practice, 2014, 1, 1
  5. You have free access to this content5
    Malco Rossi, Santiago Perez-Lloret, Daniel Cerquetti, Marcelo Merello, Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review, Movement Disorders Clinical Practice, 2014, 1, 3
  6. 6
    Edith Sturm, Nadia Stefanova, Multiple System Atrophy: Genetic or Epigenetic?, Experimental Neurobiology, 2014, 23, 4, 277

    CrossRef

  7. 7
    Maria Stamelou, Niall P. Quinn, Kailash P. Bhatia, “Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy—A diagnostic guide, Movement Disorders, 2013, 28, 9
  8. 8
    Shinsuke Fujioka, Christina Sundal, Zbigniew K Wszolek, Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics, Orphanet Journal of Rare Diseases, 2013, 8, 1, 14

    CrossRef

  9. 9
    K. Reetz, A. S. Costa, S. Mirzazade, A. Lehmann, A. Juzek, M. Rakowicz, R. Boguslawska, L. Schols, C. Linnemann, C. Mariotti, M. Grisoli, A. Durr, B. P. van de Warrenburg, D. Timmann, M. Pandolfo, P. Bauer, H. Jacobi, T.-K. Hauser, T. Klockgether, J. B. Schulz, Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6, Brain, 2013, 136, 3, 905

    CrossRef

  10. 10
    Sylvia Stemberger, Sonja W. Scholz, Andrew B. Singleton, Gregor K. Wenning, Genetic players in multiple system atrophy: unfolding the nature of the beast, Neurobiology of Aging, 2011, 32, 10, 1924.e5

    CrossRef

  11. 11
    Judith van Gaalen, Paola Giunti, Bart P. van de Warrenburg, Movement disorders in spinocerebellar ataxias, Movement Disorders, 2011, 26, 5
  12. 12
    Valentina Berti, Alberto Pupi, Lisa Mosconi, PET/CT in diagnosis of movement disorders, Annals of the New York Academy of Sciences, 2011, 1228, 1
  13. 13
    Christine Klein, Susanne A. Schneider, Anthony E. Lang, Hereditary parkinsonism: Parkinson disease look-alikes—An algorithm for clinicians to “PARK” genes and beyond, Movement Disorders, 2009, 24, 14
  14. 14
    Gregor K. Wenning, Nadia Stefanova, Recent developments in multiple system atrophy, Journal of Neurology, 2009, 256, 11, 1791

    CrossRef

  15. 15
    K. Gierga, H. J. Schelhaas, E. R. Brunt, K. Seidel, W. Scherzed, R. Egensperger, R. A. I. De Vos, W. Den Dunnen, P. F. Ippel, E. Petrasch-Parwez, T. Deller, L. Schöls, U. Rüb, Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites, Neuropathology and Applied Neurobiology, 2009, 35, 5
  16. 16
    P. Garrard, N. H. Martin, P. Giunti, L. Cipolotti, Cognitive and social cognitive functioning in spinocerebellar ataxia, Journal of Neurology, 2008, 255, 3, 398

    CrossRef

  17. 17
    Tetsutaro Ozawa, Pathology and genetics of multiple system atrophy: an approach to determining genetic susceptibility spectrum, Acta Neuropathologica, 2006, 112, 5, 531

    CrossRef

  18. 18
    Sylvia M. Boesch, Birgit Frauscher, Elisabeth Brandauer, Gregor K. Wenning, Werner Poewe, Birgit Högl, Restless legs syndrome and motor activity during sleep in spinocerebellar ataxia type 6, Sleep Medicine, 2006, 7, 6, 529

    CrossRef

  19. 19
    Alex Iranzo, Sleep in other Neurodegenerative Diseases,