1,091 results on '"Pedroso, José Luiz"'
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2. An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean
3. Clinical, neuroimaging and genetic findings in Brazilian patients with neurodegeneration with brain iron accumulation
4. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
5. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
6. Spinocerebellar ataxia type 2 has multiple ancestral origins
7. Fragile X premutation mimicking late onset hereditary spastic paraplegia
8. Immune-mediated ataxias: Guide to clinicians
9. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia
10. A Diagnostic Approach to Spastic ataxia Syndromes
11. Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
12. Subacute hemichorea and asymmetrical basal ganglia abnormalities: an archetypal scenario for anti-CV2 encephalitis
13. The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach
14. Combined assessment by transcranial sonography and Sniffin’ Sticks test has a similar diagnostic accuracy compared to brain SPECT for Parkinson's disease diagnosis.
15. Gluten Ataxia: an Overestimated Condition?
16. Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective
17. Teaching NeuroImage: Mobile Hypopyon as a Clinical Clue for the Diagnosis of Behçet Disease
18. Ataxias in Brazil: 17 years of experience in an ataxia center.
19. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
20. Teaching Video NeuroImage: TWNK Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia
21. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study
22. The clinical diagnosis of Parkinson's disease
23. Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy.
24. Family history as a clue to the diagnosis of orofacial abnormal movements in a 30-year-old man
25. A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7
26. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays
27. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
28. Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia.
29. FARS‐ADL across Ataxias: Construct Validity, Sensitivity to Change, and Minimal Important Change.
30. Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia
31. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
32. Fragile X premutation mimicking late onset hereditary spastic paraplegia
33. Cranial nerve thinning distinguishes RFC1‐related disorder from other late‐onset ataxias
34. Spinocerebellar Ataxia Type 6 and Japanese Immigration to Brazil
35. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease
36. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
37. Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach
38. Complex movement disorders associated with DEAF1 gene mutation
39. Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS
40. Expanding the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxia.
41. Cranial Nerve Thinning Distinguishes RFC1‐Related Disorder from Other Late‐Onset Ataxias.
42. Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2.
43. Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1
44. What General Neurologists Should Know about Autoinflammatory Syndromes?
45. Spinocerebellar ataxia type 2 has multiple ancestral origins
46. Juvenile Gerstmann‐Sträussler‐Scheinker disease mimicking anticipation phenomenon
47. Frequency of GAA-FGF14Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia
48. What General Neurologists Should Know about Autoinflammatory Syndromes?
49. Surgical mask-induced dyskinesia: a rare COVID-19 pandemics complication
50. Trigeminal ganglia hypoplasia as imaging clue for the diagnosis of Gómez-López-Hernández syndrome
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