Prism adaptation in spinocerebellar ataxia type 2

[1]  S. R. Jackson,et al.  Posterior parietal cortex and the dissociable components of prism adaptation , 2006, Neuropsychologia.

[2]  Benjamin Wallace,et al.  Generalization of prism adaptation. , 2006, Journal of experimental psychology. Human perception and performance.

[3]  R. Drucker-Colín,et al.  Spinocerebellar ataxia type 2 olfactory impairment shows a pattern similar to other major neurodegenerative diseases , 2006, Journal of Neurology.

[4]  Juan Fernandez-Ruiz,et al.  Rapid Topographical Plasticity of the Visuomotor Spatial Transformation , 2006, The Journal of Neuroscience.

[5]  D. Pélisson,et al.  Ipsidirectional impairment of prism adaptation after unilateral lesion of anterior cerebellum , 2005, Neurology.

[6]  Gordon M. Redding,et al.  Applications of prism adaptation: a tutorial in theory and method , 2005, Neuroscience & Biobehavioral Reviews.

[7]  S. M. Morton,et al.  Prism adaptation during walking generalizes to reaching and requires the cerebellum. , 2004, Journal of neurophysiology.

[8]  Michael Fetter,et al.  Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2 , 2004, Annals of neurology.

[9]  Thorsten Schmidt,et al.  Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis , 2004, The Lancet Neurology.

[10]  Elsdon Storey,et al.  Inter‐rater reliability of the International Cooperative Ataxia Rating Scale (ICARS) , 2004, Movement disorders : official journal of the Movement Disorder Society.

[11]  Otmar Bock,et al.  Components of sensorimotor adaptation in young and elderly subjects , 2004, Experimental Brain Research.

[12]  Y. Rossetti,et al.  Preserved prism adaptation in bilateral optic ataxia: strategic versus adaptive reaction to prisms , 2004, Experimental Brain Research.

[13]  J. Fernández-Ruiz,et al.  Normal prism adaptation but reduced after‐effect in basal ganglia disorders using a throwing task , 2003, The European journal of neuroscience.

[14]  J. Fernández-Ruiz,et al.  Olfactory dysfunction in hereditary ataxia and basal ganglia disorders , 2003, Neuroreport.

[15]  C. Globas,et al.  Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3 , 2003, Journal of Neurology.

[16]  G. M. Redding,et al.  Strategie Calibration and Spatial Alignment: A Model From Prism Adaptation , 2002, Journal of motor behavior.

[17]  Lillian Martinian,et al.  Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. , 2002, Brain : a journal of neurology.

[18]  Dottie M. Clower,et al.  Selective use of perceptual recalibration versus visuomotor skill acquisition. , 2000, Journal of neurophysiology.

[19]  C Hall,et al.  Prism adaptation in normal aging: slower adaptation rate and larger aftereffect. , 2000, Brain research. Cognitive brain research.

[20]  K. Kurata,et al.  Reacquisition deficits in prism adaptation after muscimol microinjection into the ventral premotor cortex of monkeys. , 1999, Journal of neurophysiology.

[21]  J. Baizer,et al.  Cerebellar lesions and prism adaptation in macaque monkeys. , 1999, Journal of neurophysiology.

[22]  J. Fernández-Ruiz,et al.  Prism adaptation and aftereffect: specifying the properties of a procedural memory system. , 1999, Learning & memory.

[23]  A. Federico,et al.  The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates. , 1998, Brain : a journal of neurology.

[24]  R. Miall,et al.  A study of motor performance and motor learning in episodic ataxia , 1997, NeuroReport.

[25]  Y. Agid,et al.  Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families. , 1997, Human molecular genetics.

[26]  D. Geschwind,et al.  The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. , 1997, American journal of human genetics.

[27]  M. Hallett,et al.  International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome , 1997, Journal of the Neurological Sciences.

[28]  Tracy L. Faber,et al.  Role of posterior parietal cortex in the recalibration of visually guided reaching , 1996, Nature.

[29]  W. T. Thach,et al.  Throwing while looking through prisms. II. Specificity and storage of multiple gaze-throw calibrations. , 1996, Brain : a journal of neurology.

[30]  W. T. Thach,et al.  Throwing while looking through prisms. I. Focal olivocerebellar lesions impair adaptation. , 1996, Brain : a journal of neurology.

[31]  S. Lisberger,et al.  The Cerebellum: A Neuronal Learning Machine? , 1996, Science.

[32]  A Dürr,et al.  Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families. , 1995, Brain : a journal of neurology.

[33]  Claire Gilbert Foster,et al.  International ethical guidelines for biomedical research involving human subjects , 1994 .

[34]  M. Farrall,et al.  Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. , 1990, American journal of human genetics.

[35]  Shirley Hansen,et al.  Dominantly inherited olivopontocerebellar atrophy from eastern Cuba Clinical, neuropathological, and biochemical findings , 1989, Journal of the Neurological Sciences.

[36]  R. Mayeux,et al.  Prism adaptation in Parkinson's disease. , 1988, Journal of neurology, neurosurgery, and psychiatry.

[37]  M. Hallett,et al.  Adaptation to lateral displacement of vision in patients with lesions of the central nervous system , 1983, Neurology.

[38]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.

[39]  M Glickstein,et al.  Proceedings: Role of cerebellum in prism adaptation. , 1974, The Journal of physiology.