285 results on '"Barsottini, Orlando Graziani Povoas"'
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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. Ataxias in Brazil: 17 years of experience in an ataxia center.
12. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
13. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays
14. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
15. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease
16. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
17. Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS
18. Cerebrovascular disease in patients with antiphospholipid antibody syndrome: a transcranial Doppler and magnetic resonance imaging study.
19. Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK
20. SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage
21. Central nervous system vasculitis in adults: An update
22. Should we investigate mitochondrial disorders in progressive adult-onset undetermined ataxias?
23. Functional ataxia in a specialized ataxia center
24. Structural signature in SCA1: clinical correlates, determinants and natural history
25. 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
26. Cervical and ocular vestibular evoked potentials in Machado–Joseph disease: Functional involvement of otolith pathways
27. Substantia nigra echogenicity and imaging of striatal dopamine transporters in Parkinson's disease: A cross-sectional study
28. What General Neurologists Should Know about Autoinflammatory Syndromes?
29. Psychosis in Machado–Joseph Disease: Clinical Correlates, Pathophysiological Discussion, and Functional Brain Imaging. Expanding the Cerebellar Cognitive Affective Syndrome
30. Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients
31. Substantia nigra echogenicity is correlated with nigrostriatal impairment in Machado-Joseph disease
32. Does the patient's hand hold the key to preventing secondary generalization in mesial temporal lobe epilepsy?
33. Cognitive impairment in Brazilian patients with Behçet's disease occurs independently of neurologic manifestation
34. Sleep disorders in Machado–Joseph disease: A dopamine transporter imaging study
35. Milestones in Friedreich ataxia: more than a century and still learning
36. Cognitive and olfactory deficits in Machado–Joseph disease: A dopamine transporter study
37. Epilepsy and Behçet's disease: Cortical and hippocampal involvement in Brazilian patients
38. 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
39. History and national survey on reflex hammers: which is the chosen one of Brazilian neurologists?
40. Quadrupedal gait and cerebellar hypoplasia, the Uner Tan syndrome, caused by ITPR1 gene mutation
41. Spinal cord stimulation improves motor function and gait in spastic paraplegia type 4 (SPG4): Clinical and neurophysiological evaluation
42. Paroxysmal Tonic Upward Gaze: A Clinical Clue for CACNA1A‐Related Disorders.
43. Cognitive Deficits in Machado–Joseph Disease Correlate with Hypoperfusion of Visual System Areas
44. Atypical manifestations in Brazilian patients with neuro-Behçet’s disease
45. Cerebellar Cognitive Affective Syndrome in Machado Joseph Disease: Core Clinical Features
46. Sleep Disorders in Machado–Joseph Disease: Frequency, Discriminative Thresholds, Predictive Values, and Correlation with Ataxia-Related Motor and Non-Motor Features
47. Huntington's disease as an unexpected cause of deafness with dystonia and chorea
48. Phelan-McDermid syndrome presenting with autistic spectrum: are we underdiagnosing chromosomal diseases in patients with autism?
49. Early-onset familial Alzheimer’s disease related to presenilin 1 mutation resembling autosomal dominant spinocerebellar ataxia
50. Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy.
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