25 results on '"Barsottini, Orlando Graziani Povoas"'
Search Results
2. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
3. Combined assessment by transcranial sonography and Sniffin’ Sticks test has a similar diagnostic accuracy compared to brain SPECT for Parkinson's disease diagnosis.
4. Quadrupedal gait and cerebellar hypoplasia, the Uner Tan syndrome, caused by ITPR1 gene mutation
5. ANTI-MA2 encephalitis mimicking diencephalic demyelinating syndrome
6. Spinal cord stimulation improves motor function and gait in spastic paraplegia type 4 (SPG4): Clinical and neurophysiological evaluation
7. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays
8. Huntington's disease as an unexpected cause of deafness with dystonia and chorea
9. SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage
10. Central nervous system vasculitis in adults: An update
11. 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
12. ACTH-induced dyskinesia in a child with West syndrome (infantile spasms)
13. Spontaneous downbeat nystagmus as a clue for the diagnosis of ataxia associated with anti-GAD antibodies
14. Cervical and ocular vestibular evoked potentials in Machado–Joseph disease: Functional involvement of otolith pathways
15. SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group
16. Urbach-Wiethe disease presenting with partial seizures, skin lesions and typical neuroimaging features
17. Substantia nigra echogenicity and imaging of striatal dopamine transporters in Parkinson's disease: A cross-sectional study
18. Adult onset Alexander disease presenting with progressive spastic paraplegia
19. Substantia nigra echogenicity is correlated with nigrostriatal impairment in Machado-Joseph disease
20. Does the patient's hand hold the key to preventing secondary generalization in mesial temporal lobe epilepsy?
21. Cognitive impairment in Brazilian patients with Behçet's disease occurs independently of neurologic manifestation
22. Sleep disorders in Machado–Joseph disease: A dopamine transporter imaging study
23. Cognitive and olfactory deficits in Machado–Joseph disease: A dopamine transporter study
24. Epilepsy and Behçet's disease: Cortical and hippocampal involvement in Brazilian patients
25. Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.