All Stories

  1. Neuropathology of central nervous system involvement in TTR amyloidosis
  2. Cadherin‐3 is a novel oncogenic biomarker with prognostic value in glioblastoma
  3. Peripheral neuropathy in Parkinson’s disease: prevalence and functional impact on gait and balance
  4. PD-L1 tumor expression is associated with poor prognosis and systemic immunosuppression in glioblastoma
  5. T2-FLAIR mismatch sign: a roadmap of pearls and pitfalls
  6. CNS Involvement in Hereditary Transthyretin Amyloidosis
  7. Cadherin Expression and EMT: A Focus on Gliomas
  8. Association Between Iron-Related Protein Lipocalin 2 and Cognitive Impairment in Cerebrospinal Fluid and Serum
  9. Advantages of an Automated Method Compared With Manual Methods for the Quantification of Intraepidermal Nerve Fiber in Skin Biopsy
  10. Adult polyglucosan body disease—an atypical compound heterozygous with a novel GBE1 mutation
  11. Peripheral neuropathy in systemic vasculitis and other autoimmune diseases – a report of five cases emphasizing the importance of etiologic characterization
  12. Letter to the Editor on “Copathology in Progressive Supranuclear Palsy: Does It Matter?”
  13. Diagnosis of Aicardi‐Goutières Syndrome in Adults: A Case Series
  14. Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia
  15. Brain biopsy in suspected non-neoplastic neurological disease
  16. Proinflammatory and anti-inflammatory cytokines in the CSF of patients with Alzheimer's disease and their correlation with cognitive decline
  17. Structural and molecular correlates of cognitive aging in the rat
  18. Clinicopathological correlations of sural nerve biopsies in TTR Val30Met familial amyloid polyneuropathy
  19. When Decrease Aβ1-42 in CSF May Not Mean Alzheimer's Disease
  20. Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery
  21. The etiology of spontaneous intracerebralhemorrhage: Insights from a neuropathological series
  22. Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study
  23. Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
  24. Supratentorial hemangioblastomas in von Hippel–Lindau wild-type patients – case series and literature review
  25. Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene
  26. Frontotemporal lobar degeneration-TDP with ‘multiple system atrophy phenocopy syndrome’
  27. Vascular Pathology Causing Late Onset Generalized Chorea: A Clinico-Pathological Case Report
  28. Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review
  29. Reply
  30. Clinical, biochemical, molecular, and histological features of 65 Portuguese patients with mitochondrial disorders
  31. Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome
  32. RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre
  33. Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration
  34. Post-mortem assessment in vascular dementia: advances and aspirations
  35. Interplay between aging and neuroinflammation in Alzheimer´s disease
  36. Nonprimary Cytomegalovirus Fetal Infection
  37. DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology
  38. New massive parallel sequencing approach improves the genetic characterization of congenital myopathies
  39. Appendectomy may delay Parkinson's disease Onset
  40. Chondroma of the Cerebral Falx: Case Report of a Very Rare Intracranial Tumor
  41. Neuropatia da Doença de Hansen: Um Diagnóstico a Considerar na Investigação da Neuropatia Periférica
  42. New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing
  43. Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
  44. Familial amyloid polyneuropathy
  45. CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings
  46. Ryanodine Myopathies Without Central Cores—Clinical, Histopathologic, and Genetic Description of Three Cases
  47. PARK2 presenting as a disabling peripheral axonal neuropathy
  48. Acute Ischemic Stroke Secondary to Glioblastoma
  49. Freezing of gait – First motor manifestation in late infantile variant neuronal ceroid lipofuscinosis
  50. Genetic Analysis of Inherited Leukodystrophies
  51. Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency
  52. Multiple cerebral infarcts and intravascular central nervous system lymphoma: A rare but potentially treatable association
  53. Hereditary Neuropathy with Liability to Pressure Palsy: A Recurrent and Bilateral Foot Drop Case Report
  54. Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database
  55. Clinical, Neuropathological, and Genetic Characteristics of the Novel IVS9+1delG GRN Mutation in a Patient with Frontotemporal Dementia
  56. TTC7B Emerges as a Novel Risk Factor for Ischemic Stroke Through the Convergence of Several Genome-Wide Approaches
  57. Permanent dysphagia in familial amyloid polyneuropathy (ATTRVal30Met)
  58. Sporadic hemiplegic migraine with normal imaging as the initial manifestation of CADASIL
  59. Clinico-Pathological Correlations of the Most Common Neurodegenerative Dementias
  60. Gliomatosis Cerebri Diagnostic Challenge
  61. Primary antiphospholipid antibody syndrome presenting with encephalopathy, psychosis and seizures
  62. Acute hemorrhagic leukoencephalitis with severe brainstem and spinal cord involvement: MRI features with neuropathological confirmation
  63. Medulloblastoma and gliomatosis cerebri: rare brain tumors in multiple sclerosis patients
  64. Task-specific contribution of the human striatum to perceptual–motor skill learning
  65. A case of haemophagocytic syndrome presenting with oculogyric crises
  66. Adult-onset dystonia in Aicardi-Goutières syndrome
  67. Kalirin: a novel genetic risk factor for ischemic stroke
  68. Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients
  69. Streptococcus suis meningitis: First case report from Portugal
  70. Specific Configuration of Dendritic Degeneration in Pyramidal Neurons of the Medial Prefrontal Cortex Induced by Differing Corticosteroid Regimens
  71. Morphological Correlates of Corticosteroid-Induced Changes in Prefrontal Cortex-Dependent Behaviors