310 results on '"Vale, Thiago Cardoso"'
Search Results
2. A Diagnostic Approach to Spastic ataxia Syndromes
3. Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
4. Family history as a clue to the diagnosis of orofacial abnormal movements in a 30-year-old man
5. Parkinsonism in a population-based study of individuals aged 75+ years: The Pietà study
6. Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1
7. Phenylketonuria in three siblings
8. Incidence Rate and Factors Associated with Delirium and Subsyndromal Delirium in Patients with COVID-19 in an Intensive Care Unit
9. Teaching Video NeuroImages: Hemichorea-hemiballismus secondary to nonketotic hyperglycemia
10. Movement disorders in hereditary spastic paraplegias
11. Handicap as a Measure of Perceived‐Health Status in Parkinson's Disease.
12. Dystonia, Chorea, and Ataxia: Three Challenging Cases
13. Fragile X-associated tremor or ataxia syndrome in a patient with difficulty walking, falls, a tremor, and erectile dysfunction
14. Perioral and tongue fasciculations in Kennedy’s disease
15. Teaching NeuroImages: Spinocerebellar ataxia type 3 presenting with a cock-walk gait phenotype
16. Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia
17. Optical coherence tomography in neurodegenerative disorders
18. A Diagnostic Approach to Spastic ataxia Syndromes
19. Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
20. Limb myorhythmia from spinal cord glioma
21. Obstructive Hydrocephalous Presenting with Bobble-Head Doll Syndrome
22. Clinicoradiological comparison between vascular parkinsonism and Parkinson’s disease
23. Painful legs and moving toes
24. Hypertrophic cervical spinal cord pachymeningitis due to Treponema pallidum infection
25. Weil Syndrome: A Rare Cause of Cerebral Venous Thrombosis
26. Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia.
27. Headache Prevalence in a Specialized Center
28. Doctor, I Had a Terrible Headache. What Is My Diagnosis?
29. Cranial hypertrophic pachymeningitis secondary to neurocysticercosis
30. Multiple myeloma with cauda equina infiltration
31. Superficial Siderosis, Traumatic Tap, and Xanthochromia—Reply
32. Neurosyphilis presenting as mania
33. Late-onset hummingbird sign in a woman with fragile X premutation
34. Idiopathic Superficial Siderosis
35. Schistosoma mansoni Encephalomyelitis
36. Facial grimacing and clinical correlates in spinocerebellar ataxia type 3
37. Huntington’s disease-like 2: a phenocopy not to miss
38. Symptomatic female carriers of mutations in the Duchenne muscular dystrophy gene
39. Postsurgical Myoclonus of the Pectoralis Major
40. No Correlation Between White Matter Changes and Mild Parkinsonian Signs in Individuals Aged Older Than 75 Years
41. Complex Movement Disorders in Ataxia with Oculomotor Apraxia Type 1: Beyond the Cerebellar Syndrome
42. Expanding the Phenotype of Dystonia‐Deafness Syndrome Caused by ACTB Gene Mutation
43. Acute cerebellar ataxia: differential diagnosis and clinical approach
44. Hemiballismus secondary to metastatic breast cancer
45. Cerebellar degeneration and progressive ataxia associated with HIV-virus infection
46. SPG7 with parkinsonism responsive to levodopa and dopaminergic deficit
47. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia
48. Stroke after lung biopsy
49. Acute cerebellar ataxia: differential diagnosis and clinical approach
50. Atypical clinical presentation in an anterior cerebral artery territory infarction
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