480 results on '"Barsottini, Orlando Graziani Povoas"'
Search Results
2. Tract-specific spinal damage in SCA2, SCA3 and SCA6
3. Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11
4. Frequency of anti-MOG antibodies in serum and CSF of patients with possible autoimmune encephalitis: Results from a Brazilian multicentric study
5. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
6. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
7. A Diagnostic Approach to Spastic ataxia Syndromes
8. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia
9. Combined assessment by transcranial sonography and Sniffin’ Sticks test has a similar diagnostic accuracy compared to brain SPECT for Parkinson's disease diagnosis.
10. The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach
11. Cerebrovascular disease in patients with antiphospholipid antibody syndrome: a transcranial Doppler and magnetic resonance imaging study
12. Ataxias in Brazil: 17 years of experience in an ataxia center.
13. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
14. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays
15. Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy.
16. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
17. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease
18. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
19. Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS
20. Atypical Parkinsonism
21. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
22. Complex movement disorders in early onset hypoparathyroidism
23. Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK
24. SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage
25. Spinocerebellar Ataxia Type 6 and Japanese Immigration to Brazil
26. Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1
27. What General Neurologists Should Know about Autoinflammatory Syndromes?
28. Juvenile Gerstmann‐Sträussler‐Scheinker disease mimicking anticipation phenomenon
29. Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations
30. Central nervous system vasculitis in adults: An update
31. Should we investigate mitochondrial disorders in progressive adult-onset undetermined ataxias?
32. Functional ataxia in a specialized ataxia center
33. Structural signature in SCA1: clinical correlates, determinants and natural history
34. Surgical mask-induced dyskinesia: a rare COVID-19 pandemics complication
35. Paroxysmal Tonic Upward Gaze: A Clinical Clue for CACNA1A‐Related Disorders
36. One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia
37. History and national survey on reflex hammers: which is the chosen one of Brazilian neurologists?
38. Cervical and ocular vestibular evoked potentials in Machado–Joseph disease: Functional involvement of otolith pathways
39. Cerebellar Cognitive Affective/Schmahmann Syndrome Scale--Brazilian Portuguese Version
40. Substantia nigra echogenicity and imaging of striatal dopamine transporters in Parkinson's disease: A cross-sectional study
41. Psychosis in Machado–Joseph Disease: Clinical Correlates, Pathophysiological Discussion, and Functional Brain Imaging. Expanding the Cerebellar Cognitive Affective Syndrome
42. Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients
43. Conus medullaris syndrome in Vogt-Koyanagi-Harada disease: an unusual presentation
44. Substantia nigra echogenicity is correlated with nigrostriatal impairment in Machado-Joseph disease
45. Does the patient's hand hold the key to preventing secondary generalization in mesial temporal lobe epilepsy?
46. Cognitive impairment in Brazilian patients with Behçet's disease occurs independently of neurologic manifestation
47. Sleep disorders in Machado–Joseph disease: A dopamine transporter imaging study
48. Multiple cerebral cavernomas in linear scleroderma: an unusual association
49. Milestones in Friedreich ataxia: more than a century and still learning
50. Cognitive and olfactory deficits in Machado–Joseph disease: A dopamine transporter study
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