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48 results on '"Barsottini, Orlando Graziani Povoas"'

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1. Does the patient's hand hold the key to preventing secondary generalization in mesial temporal lobe epilepsy?

2. Tract-specific spinal damage in SCA2, SCA3 and SCA6.

4. Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil.

5. Hereditary Truncal Dystonia Associated with ANO3 Gene Variant.

6. What General Neurologists Should Know about Autoinflammatory Syndromes?

7. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale.

8. Paroxysmal Tonic Upward Gaze: A Clinical Clue for CACNA1A‐Related Disorders.

9. A Diagnostic Approach to Spastic ataxia Syndromes.

10. The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach.

11. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia.

12. Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy.

13. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias.

15. Spinocerebellar Ataxia Type 6 and Japanese Immigration to Brazil.

16. Spinal cord stimulation improves motor function and gait in spastic paraplegia type 4 (SPG4): Clinical and neurophysiological evaluation.

17. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study.

18. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays.

19. Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders.

20. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease.

21. Functional ataxia in a specialized ataxia center.

23. Reconstructing the History of Machado-Joseph Disease.

24. Huntington's disease as an unexpected cause of deafness with dystonia and chorea.

26. Structural signature in SCA1: clinical correlates, determinants and natural history.

27. SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response.

28. Structural signature of SCA3: From presymptomatic to late disease stages.

30. Central nervous system vasculitis in adults: An update.

31. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale.

32. 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.

33. A Woman with Progressive Ataxia and Abnormal Eye Movements.

35. Cervical and ocular vestibular evoked potentials in Machado–Joseph disease: Functional involvement of otolith pathways.

36. SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group.

37. Substantia nigra echogenicity and imaging of striatal dopamine transporters in Parkinson's disease: A cross-sectional study.

38. Substantia nigra echogenicity is correlated with nigrostriatal impairment in Machado-Joseph disease.

39. Cognitive impairment in Brazilian patients with Behçet's disease occurs independently of neurologic manifestation

40. Sleep disorders in Machado–Joseph disease: A dopamine transporter imaging study

41. Cognitive and olfactory deficits in Machado–Joseph disease: A dopamine transporter study

42. Epilepsy and Behçet's disease: Cortical and hippocampal involvement in Brazilian patients

43. Is Neuropathy Involved with Restless Legs Syndrome in Machado-Joseph Disease?

44. Pyramidal tract degeneration in multiple system atrophy: The relevance of magnetization transfer imaging.

46. Spontaneous downbeat nystagmus as a clue for the diagnosis of ataxia associated with anti-GAD antibodies.

47. ACTH-induced dyskinesia in a child with West syndrome (infantile spasms).

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