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  1. Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran‐Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly)
  2. Patisiran in ATTRv amyloidosis with polyneuropathy: “PatisiranItaly” multicenter observational study
  3. Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy
  4. Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy
  5. Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth disease
  6. Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study
  7. Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome
  8. Magnetic resonance neurography and diffusion tensor imaging of the sciatic nerve in hereditary transthyretin amyloidosis polyneuropathy
  9. Risk of disease relapse, safety and tolerability of SARS‐CoV‐2 vaccination in patients with chronic inflammatory neuropathies
  10. Vasculitic flare in a patient with anti-myelin-associated glycoprotein (MAG) antibody following mRNA-1273 SARS-CoV-2 vaccine
  11. Aducanumab for the treatment of Alzheimer's disease
  12. Correction: Olfactory swab sampling optimization for α-synuclein aggregate detection in patients with Parkinson’s disease
  13. Olfactory swab sampling optimization for α-synuclein aggregate detection in patients with Parkinson’s disease
  14. Association between inflammatory central nervous system lesions and Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome (CANVAS): a case series
  15. Italian Real-Life Experience of Patients with Hereditary Transthyretin Amyloidosis Treated with Patisiran
  16. Real‐life experience with inotersen in hereditary transthyretin amyloidosis with late‐onset phenotype: Data from an early‐access program in Italy
  17. Neuropathic pain in Charcot–Marie‐Tooth disease: A clinical and laser‐evoked potential study
  18. Ischemic stroke due to sporadic and genetic pulmonary arteriovenous malformations
  19. Featured Cover
  20. Hereditary neuropathies: A pathological perspective
  21. Clinical and pathological characterization of RFC1 AAGGG expansion presenting as chronic axonal polyneuropathy
  22. RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy
  23. Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy
  24. Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies
  25. Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult‐onset Krabbe disease
  26. Mechanisms of Nerve Damage in Neuropathies Associated with Hematological Diseases: Lesson from Nerve Biopsies
  27. Hypothalamic-Bulbar MRI Hyperintensity in Anti-IgLON5 Disease with Serum-Restricted Antibodies: A Case Report and Systematic Review of Literature
  28. hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers
  29. Neuroimaging Findings in Chronic Hepatitis C Virus Infection: Correlation with Neurocognitive and Neuropsychiatric Manifestations
  30. Myelin uncompaction and axo‐glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b
  31. QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations
  32. Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis
  33. Microglial and Neuronal TDP-43 Pathology in Anti-IgLON5-Related Tauopathy
  34. Percutaneous alcohol injection under sonographic guidance in Morton’s neuroma: follow-up in 220 treated lesions
  35. A Simplified Callosal Angle Measure Best Differentiates Idiopathic-Normal Pressure Hydrocephalus from Neurodegenerative Dementia
  36. Accuracy of Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease Among Rapidly Progressive Dementia