213 results on '"Nóbrega, Paulo Ribeiro"'
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2. Identifying high-risk neurological phenotypes in adult-onset classic monogenic autoinflammatory diseases: when should neurologists consider testing?
3. Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy
4. Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11
5. Frequency of anti-MOG antibodies in serum and CSF of patients with possible autoimmune encephalitis: Results from a Brazilian multicentric study
6. Sleep disorders in cerebrotendinous xanthomatosis: A case series
7. Controversies in immunotherapy for anti-NMDA receptor encephalitis: a scoping review with a proposal of operational definitions
8. New observations on minifascicular neuropathy with sex-dependent gonadal dysgenesis: a case series with nerve ultrasound assessment
9. Spinocerebellar ataxia type 2 has multiple ancestral origins
10. Persistent psychosis associated with extreme delta brush in anti-NMDA receptor encephalitis: a case report
11. Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
12. Correlation between ABO blood type, susceptibility to SARS-CoV-2 infection and COVID-19 disease severity: A systematic review
13. Aseptic meningitis in Fabry disease due to a novel GLA variant: an expanded phenotype?
14. Characteristics and management of Susac syndrome in an emergent country: a multi-center case series from Brazil
15. Polyneuropathy in Cerebrotendinous Xanthomatosis: Diagnostic Challenges and Potential for Therapeutic Intervention.
16. Myasthenia gravis exacerbation and myasthenic crisis associated with COVID-19: case series and literature review
17. Moyamoya associated with Turner syndrome in a patient with type 2 spinocerebellar ataxia—Occam’s razor or Hickam’s dictum: a case report
18. Normal pressure hydrocephalus associated with COVID-19 infection: a case report
19. Central hypersomnia and chronic insomnia: expanding the spectrum of sleep disorders in long COVID syndrome - a prospective cohort study
20. Characterization of Headache in COVID-19: a Retrospective Multicenter Study
21. Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale
22. Letter response to “The Janus faces of SARS-COV-2 infection in myasthenia gravis and myasthenic crisis”
23. Intracranial mass lesions and skin discoloration in the armpits as unusual clues to Erdheim-Chester disease: a case report
24. Steroid responsive cavernous sinus syndrome due to Rosai-Dorfman disease: beyond Tolosa-Hunt syndrome – a case report
25. Editorial for Brain Sciences Special Issue: “Neurogenetic Disorders across Human Life: From Infancy to Adulthood”
26. Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report
27. Peculiar aetiology for orbital apex syndrome: Wyburn-Mason syndrome as orbital apex lesion
28. Caffeine as adjuvant therapy for Tension-Type Headache: A systematic review
29. Higher Prevalence of Nonsense Pathogenic DMD Variants in a Single-Center Cohort from Brazil: A Genetic Profile Study That May Guide the Choice of Disease-Modifying Treatments
30. Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy
31. Pompe disease misdiagnosed as polymyositis
32. Pregabalin Responsive Tongue and Arm Tremor after Guillain Barré Syndrome
33. Spinal cord compression by cystic IgG4-related spinal pachymeningitis mimicking neurocysticercosis: a case report
34. Bailey-Bloch Congenital Myopathy in Brazilian Patients: A Very Rare Myopathy with Malignant Hyperthermia Susceptibility
35. Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations
36. Pathophysiology and Treatment of Lipid Abnormalities in Cerebrotendinous Xanthomatosis: An Integrative Review
37. A case of mitochondrial DNA depletion syndrome type 11 – expanding the genotype and phenotype
38. Ceroid lipofuscinosis type 5: novel pathogenic variants and unexpected phenotypic findings
39. Immunoglobulin-responsive chikungunya encephalitis: two case reports
40. Diagnóstico por imagem de arteriopatia cerebral associada a mutação ACTA2: relato de caso
41. Response letter to: a homozygous p.Val120Leu (c.358G > C) SOD1 mutation led to slowly progressive amyotrophic lateral sclerosis in a Brazilian family.
42. Cerebellar Cognitive Affective/Schmahmann Syndrome Scale--Brazilian Portuguese Version
43. Cerebrotendinous Xanthomatosis: A practice review of pathophysiology, diagnosis, and treatment
44. Correlation between ABO blood type, susceptibility to SARS-CoV-2 infection and COVID-19 disease severity: A systematic review
45. Nutritional status and eating habits of patients with hereditary ataxias: a case–control study.
46. Mystery solved after 23 years: M syndrome is PIGT ‐associated multiple congenital anomalies‐hypotonia‐seizures syndrome 3
47. Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
48. Neuropsychological Characterization of Autosomal Recessive Intellectual Developmental Disorder 59 Associated with IMPA1 (MRT59).
49. Adult-onset subacute sclerosing panencephalitis manifesting as slowly progressive dementia
50. Nutritional status and eating habits of patients with hereditary ataxias: a case–control study
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