22 results on '"Barsottini, Orlando Graziani Povoas"'
Search Results
2. Tract-specific spinal damage in SCA2, SCA3 and SCA6
3. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
4. A Diagnostic Approach to Spastic ataxia Syndromes
5. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia
6. The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach
7. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
8. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
9. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease
10. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
11. Should we investigate mitochondrial disorders in progressive adult-onset undetermined ataxias?
12. Structural signature in SCA1: clinical correlates, determinants and natural history
13. Psychosis in Machado–Joseph Disease: Clinical Correlates, Pathophysiological Discussion, and Functional Brain Imaging. Expanding the Cerebellar Cognitive Affective Syndrome
14. Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients
15. Milestones in Friedreich ataxia: more than a century and still learning
16. Neurophysiological Studies and Non-Motor Symptoms Prior to Ataxia in a Patient with Machado–Joseph Disease: Trying to Understand the Natural History of Brain Degeneration
17. Cognitive Deficits in Machado–Joseph Disease Correlate with Hypoperfusion of Visual System Areas
18. Atypical manifestations in Brazilian patients with neuro-Behçet’s disease
19. Cerebellar Cognitive Affective Syndrome in Machado Joseph Disease: Core Clinical Features
20. Sleep Disorders in Machado–Joseph Disease: Frequency, Discriminative Thresholds, Predictive Values, and Correlation with Ataxia-Related Motor and Non-Motor Features
21. Phelan-McDermid syndrome presenting with autistic spectrum: are we underdiagnosing chromosomal diseases in patients with autism?
22. Early-onset familial Alzheimer’s disease related to presenilin 1 mutation resembling autosomal dominant spinocerebellar ataxia
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