Showing 1 - 20 results of 20 for search 'DYSTONIA', query time: 0.51s Refine Results
  1. 1
    Models of Epsilon-Sarcoglycan Gene Inactivation and their Implications for the Pathology of Myoclonus Dystonia
    by Given, Alexis
    Published 2013
    Subjects: “...Myoclonus Dystonia...”
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  2. 2
    Models of Epsilon-Sarcoglycan Gene Inactivation and their Implications for the Pathology of Myoclonus Dystonia
    by Given, Alexis
    Published 2013
    Subjects: “...Myoclonus Dystonia...”
    Get full text
  3. 3
    Models of Epsilon-Sarcoglycan Gene Inactivation and their Implications for the Pathology of Myoclonus Dystonia
    by Given, Alexis
    Published 2013
    Subjects: “...Myoclonus Dystonia...”
    Get full text
    Get full text
  4. 4
    Elucidating the Biological Role of Neuronal Dystonin Isoforms in the Hereditary Sensory Neuropathy Dystonia Musculorum
    by Ferrier, Andrew R.
    Published 2013
    “...Dystonin is a cytoskeletal linker protein whose loss-of-function in dystonia musculorum (dt) mice...”
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  5. 5
    Elucidating the Biological Role of Neuronal Dystonin Isoforms in the Hereditary Sensory Neuropathy Dystonia Musculorum
    by Ferrier, Andrew R.
    Published 2013
    “...Dystonin is a cytoskeletal linker protein whose loss-of-function in dystonia musculorum (dt) mice...”
    Get full text
    Get full text
  6. 6
    Identification, Validation and Characterization of the Mutation on Chromosome 18p which is Responsible for Causing Myoclonus-Dystonia
    by Vanstone, Megan
    Published 2012
    Subjects: “...Myoclonus-Dystonia...”
    Get full text
  7. 7
    Identification, Validation and Characterization of the Mutation on Chromosome 18p which is Responsible for Causing Myoclonus-Dystonia
    by Vanstone, Megan
    Published 2012
    Subjects: “...Myoclonus-Dystonia...”
    Get full text
  8. 8
    Identification, Validation and Characterization of the Mutation on Chromosome 18p which is Responsible for Causing Myoclonus-Dystonia
    by Vanstone, Megan
    Published 2012
    Subjects: “...Myoclonus-Dystonia...”
    Get full text
    Get full text
  9. 9
    Investigating the Relationship and Potential Interactions of CD108131 and SGCE
    by Jamieson-Williams, Rhiannon
    Published 2019
    Subjects: “...dystonia...”
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    Get full text
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  10. 10
    Etude du rôle du cervelet dans la plasticité cérébrale : cas de la dystonie
    by Hubsch-Bonneaud, Cecile
    Published 2014
    Subjects: “...Dystonia...”
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  11. 11
    Les dystonies focales : leurs dysfonctionnements sensori-moteurs et leurs conséquences sur l'organisation du mouvement
    by Bleton, Jean-Pierre
    Published 2015
    Subjects: “...Dystonia...”
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  12. 12
    Dialogue cérébello-pariétal pendant l’adaptation motrice : le cas de la Dystonie
    by Richard, Aliénor
    Published 2016
    Subjects: “...Dystonia...”
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  13. 13
    Hétérogénéité génétique et allélique des dystonies, recherche de gènes candidats et validation fonctionnelle
    by Miltgen, Morgane
    Published 2016
    Subjects: “...Dystonia...”
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  14. 14
    A clinical, neurophysiological and genetic study of South African familial combined myoclonic syndromes
    by Van Coller, Riaan
    Published 2021
    “...-sarcoglycan gene causing subcortical origin, Myoclonus Dystonia Syndrome (MDS) in a three generation South...”
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    Get full text
  15. 15
    SHIP® With a client experiencing Meige’s Syndrome : a Hermeneutic Single-Case Efficacy Study
    by Steenkamp, Casper Jan Hendrik
    Published 2018
    “...SUMMARY Meige’s syndrome is classified as a rare form of focal dystonia characterized...”
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    Get full text
  16. 16
    Body, Self, Device: Nonhuman Objects and Human Identity
    by Morrison, Daniel Ray
    Published 2012
    “... in the treatment of people with movement disorders, including Parkinson's Disease, Essential Tremor, and Dystonia...”
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  17. 17
    Remodelling the genetics of spinocerebellar entities. New genes, phenotypes, and transmission modes lead to new concepts
    by Coutelier, Marie
    Published 2016
    “... implicated in a form of autosomal dominant HCA (CACNA1A), and an autosomal recessive subtype of dystonia...”
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  18. 18
    Ironing out the pathophysiology of neurodegeneration with brain iron accumulation (NBIA) : clinical investigations and disease modelling yield novel evidence of systemic dysfunction and provide a robust and accurate disease model of NBIA
    by Minkley, Michael
    Published 2018
    “... of motor symptoms (Barry-Albright Dystonia Rating Scale) making them potential candidates markers...”
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    Others
  19. 19
    Collective dynamics of basal ganglia-thalamo-cortical loops and their roles in functions and dysfunctions
    by Arakaki, Takafumi
    Published 2016
    “... or dystonia. More recent studies suggest the key role of the BG in "non-motor" diseases such as absence...”
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  20. 20
    Clinical and molecular characterisation of type I interferonopathies
    by Melki, Isabelle
    Published 2017
    “... described of the monogenic interferonopathies, exhibit dystonia, spasticity, developmental delay, intra...”
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