21st International Congress » Ataxia
Date: Wednesday, June 7, 2017
Time: 1:15pm-2:45pm
Location: Exhibit Hall C
Meeting: 21st International Congress
- 1:15pm-2:45pm
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99mTc -TRODAT- 1 SPECT SHOWING DOPAMINERGIC DEFICIENCY IN A PATIENT WITH SPINOCEREBELLAR ATAXIA TYPE 10 AND PARKINSONISM.
- 1:15pm-2:45pm
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A case report: a primary progressive multiple sclerosis (PPMS) with adolescent-onset of progressive cerebellar ataxia
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A comparative study between OCT in SCA3 and 10
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Allelic CACNA1A disorders: a retrospective cohort analysis on clinical course and overlapping features
- 1:15pm-2:45pm
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Ataxia-Teleangiectasia-Mutated-Knock-Out mouse cerebellum shows significant reduction of calcium homeostasis factors
- 1:15pm-2:45pm
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Audiological Evaluation in Sporadic Ataxia
- 1:15pm-2:45pm
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Autosomal Dominant Spinocerebellar Ataxia Secondary to CACNA1G in a Patient of German Ancestry
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Cerebellar Ataxia – The First Symptom of HIV Infection
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Corticospinal tract dysfunction precede the cerebellar syndrome in spinocerebellar ataxia 2
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Delayed progressive spastic cerebellar ataxia and cerebellar atrophy after Heat Stroke
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Early diagnosis in Spinocerebellar Ataxias: Prospects for clinical alterations and ethical dilemmas during preclinical trials.
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Effect of Virtual Reality on Balance Rehabilitation
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Effectiveness of Deep Brain Stimulation (DBS) in Mice with Spinocerebellar Ataxia (SCA1).
- 1:15pm-2:45pm
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Induced pluripotent stem cells based in-vitro modelling of Spinocerebellar Ataxia type -12 (SCA-12).
- 1:15pm-2:45pm
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Investigating the Lipidomic Signature of Spinocerebellar Ataxia (SCA1) Using A Liquid-Microjunction Surface Sampling Probe
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Living with Ataxia in Ireland 2016–a nationwide survey of 130 Irish patients with inherited Ataxia
- 1:15pm-2:45pm
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Neurotological Findings in Sporadic Ataxia
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Nutritional status and changes in body weight in patients with multiple system atrophy
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Potential preclinical gait and balance markers for developing Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)
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Quantitative evaluation of gait ataxia by triaxial accelerometers is more sensitive than SARA within 1.5 years.
- 1:15pm-2:45pm
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Spinocerebellar Ataxia type 11 in a Hispanic Kindred
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Spinocerebellar ataxia type-17: An Indian Scenario
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Steroid-responsive encephalopathy with associated thyroiditis (SREAT) presenting with pure cerebellar ataxia
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TANDEM REPEATS BEYOND THE CLINICAL DIAGNOSIS IN ADCAs
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Targeting the intracellular localization of Ataxin-3 as novel treatment strategy for Spinocerebellar Ataxia Type 3
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The diagnostic dilemma of olivopontocerebellar atrophy and spinocerebellar ataxia, a comparative analysis of clinical cases.