1,105 results on '"Pedroso, José Luiz"'
Search Results
2. Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11
3. The GENESIS database and tools: A decade of discovery in Mendelian genomics
4. Clinical, neuroimaging and genetic findings in Brazilian patients with neurodegeneration with brain iron accumulation
5. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
6. An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean
7. Spinocerebellar ataxia type 2 has multiple ancestral origins
8. Fragile X premutation mimicking late onset hereditary spastic paraplegia
9. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
10. Immune-mediated ataxias: Guide to clinicians
11. A Diagnostic Approach to Spastic ataxia Syndromes
12. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia
13. Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
14. Subacute hemichorea and asymmetrical basal ganglia abnormalities: an archetypal scenario for anti-CV2 encephalitis
15. The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach
16. Combined assessment by transcranial sonography and Sniffin’ Sticks test has a similar diagnostic accuracy compared to brain SPECT for Parkinson's disease diagnosis.
17. Gluten Ataxia: an Overestimated Condition?
18. Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective
19. Teaching NeuroImage: Mobile Hypopyon as a Clinical Clue for the Diagnosis of Behçet Disease
20. Teaching Video NeuroImage: TWNK Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia
21. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
22. Family history as a clue to the diagnosis of orofacial abnormal movements in a 30-year-old man
23. A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7
24. Ataxias in Brazil: 17 years of experience in an ataxia center.
25. The clinical diagnosis of Parkinson's disease.
26. Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia.
27. FARS‐ADL across Ataxias: Construct Validity, Sensitivity to Change, and Minimal Important Change.
28. Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays
29. Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia
30. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study
31. Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy.
32. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
33. Childhood-onset writer's cramp and cerebellar ataxia: A neurological conundrum
34. Fragile X premutation mimicking late onset hereditary spastic paraplegia
35. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
36. Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease
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. Cranial nerve thinning distinguishes RFC1‐related disorder from other late‐onset ataxias
41. Spinocerebellar Ataxia Type 6 and Japanese Immigration to Brazil
42. Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1
43. What General Neurologists Should Know about Autoinflammatory Syndromes?
44. Spinocerebellar ataxia type 2 has multiple ancestral origins
45. Rehabilitation of Ataxia
46. Multimodal neuroimaging analysis in patients with SYNE1 Ataxia
47. Trigeminal ganglia hypoplasia as imaging clue for the diagnosis of Gómez-López-Hernández syndrome
48. Cognitive and Psychiatric Evaluation in SYNE1 Ataxia
49. Selective Forces Related to Spinocerebellar Ataxia Type 2
50. Functional ataxia in a specialized ataxia center
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