• A case of HTLV-1 associated myelopathy progressed in course over 30 years
• A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness
• Allgrove syndrome (triple A). Finding of a mutation not described in the AAAS gene
• An epidemic in Cuba of optic neuropathy, sensorineural deafness, peripheral sensory neuropathy and dorsolateral myeloneuropathy
• Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function
• Broadening the phenotype of the TWNK gene associated Perrault syndrome
• Community-based study of neurological disorders in rural central Ethiopia
• Familial spastic paraparesis and deafness. A new x-linked neurodegenerative disorder
• Idiopathic superficial siderosis of the central nervous system
• Low HTLV-1 seroprevalence in endemic tropical spastic paraparesis in Ethiopia
• Multi-system neurological disease is common in patients with OPA1 mutations
• Neurobrucellosis
• Neurological disorders associated with cassava diet: a review of putative etiological mechanisms
• Novel <em>SERAC1</em> Variant Presenting With Adult-Onset Extrapyramidal Dystonia-Parkinsonism Phenotype: A Case Report
• Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations
• POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients
• SERAC1 Deficiency- A New Phenotype
• Spastic paraparesis and sensorineural hearing loss in a patient with neurobrucellosis
• Spinocerebellar ataxia associated with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesis in two brothers
• Spinocerebellar ataxia with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesis
• Superficial siderosis of the central nervous system
• Superficial siderosis of the central nervous system: an uncommon cause of spastic paraparesia