• <em>RNASEH2B</em> Pathogenic Mutation Presenting with Pure, Apparently Non-Progressive Hereditary Spastic Paraparesis
• A Clinical Neurological Approach to the Child With Adenosine Deaminase Deficiency
• A historical look using virtual microscopy: the first case report of adrenomyeloneuropathy (AMN)
• A new phenotype of TUBB4A mutation in a family with adult-onset progressive spastic paraplegia and isolated hypomyelination leukodystrophy: A case report and literature review
• A Novel <em>SPAST</em> Variant Associated with Isolated Spastic Paraplegia
• A Novel Homozygous <em>ACBD5</em> Variant in an Emerging Peroxisomal Disorder Presenting with Retinal Dystrophy and a Review of the Literature
• A novel SPAST gene splicing variant (c.1617-2A>C) in a heterozygous carrier with hereditary spastic paraplegia
• A Novel SPAST Variant Associated with Isolated Spastic Paraplegia
• A rare case of adult-onset spastic paraparesis associated with Klinefelter syndrome
• A Textbook Case of Human T-lymphotropic Virus-1 (HTLV-1)-Induced Adult T-cell Leukemia Treated With Cyclophosphamide, Hydroxydaunorubicin, Oncovin, and Prednisone/Prednisolone (CHOP)
• Advances in the treatment of human T-cell lymphotropic virus type-I associated myelopathy
• An HTLV-1 envelope mRNA vaccine is immunogenic and protective in New Zealand rabbits
• An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review
• Anti-HTLV-1 immunity combined with proviral load as predictive biomarkers for adult T-cell leukemia-lymphoma
• Association between Brain White Matter Lesions and Disease Activity in HAM/TSP Patients
• Behr's syndrome mimicking a case of hereditary spastic paraparesis
• Blood-borne viruses and neurological manifestations: An overview
• Burden of illness and mortality in men with Adrenomyeloneuropathy: a retrospective cohort study
• Cannabinoid receptors as new targets for HTLV-1 associated myelopathy (HAM/TSP) treatment
• Complete Rescue of HTLV-1_p12KO Infectivity by Depletion of Monocytes Together with NK and CD8⁺ T Cells
• Comprehensive Insight into the Functional Roles of NK and NKT Cells in HTLV-1-Associated Diseases and Asymptomatic Carriers
• COQ7 splice site variant causing a spastic paraparesis phenotype in siblings
• Correction: Performance of the national institute of infectious diseases disability scale in HTLV-1-associated myelopathy/tropical spastic paraparesis
• Decoding dysregulated angiogenesis in HTLV-1 asymptomatic carriers compared to healthy individuals
• Determination of molecular epidemiologic pattern of human T-lymphotropic virus type 1 (HTLV-1) in Alborz province, Iran
• Developmental and epileptic encephalopathy produced by the ATP1A2 mutation
• Differential modulation of IL-4, IL-10, IL-17, and IFN-γ production mediated by IgG from Human T-lymphotropic virus-1 (HTLV-1) infected patients on healthy peripheral T (CD4+, CD8+, and γδ) and B cells
• Discovery of a Novel Yadav-Kunal Reflex in Context of Upper Motor Neuron Lesions: A Report of Three Cases
• Disseminated Cavernous Malformations Due to KRIT1 Gene Mutation Causing Seizure and Spastic Paraparesis
• Early-onset familial Alzheimer's disease with spastic paraparesis associated with PSEN1 gene
• Effectiveness of repeated injections of botulinum toxin A on gait and fatigue in adults with spastic paraparesis secondary to multiple sclerosis
• Effects of HTLV-1 on leukocyte trafficking and migration in ACs compared to healthy individuals
• Epidemiological and clinical profile of HTLV-1 patients: a closer look at a reference center in Bahia, Brazil
• Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia
• Founder SPG11 Mutation in the Baniya Community of India
• Gait analysis patterns and rehabilitative interventions to improve gait in persons with hereditary spastic paraplegia: a systematic review and meta-analysis
• Hepatic myelopathy neurological complication of chronic liver disease: two case reports
• Hereditary spastic paraparesis due to SPG5/CYP7B1 mutation with potential therapeutic implications
• Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability
• Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature
• Hereditary Spastic Paraplegia Type 11-Clinical, Genetic and Neuroimaging Characteristics
• Higher expression of BRCA1, and CHUK and lower expression of NFKBIA, ESR1, PIK3R1, and PPARG in HAM/TSP compared to ATLL, a diverse pathological consequence
• HLA-A*24 Increases the Risk of HTLV-1-Associated Myelopathy despite Reducing HTLV-1 Proviral Load
• How do socioeconomic determinants of health affect the likelihood of living with HTLV-1 globally? A systematic review with meta-analysis
• HTLV in Sweden
• HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP): Case based discussion of risk factors, clinical, and therapeutic considerations
• HTLV-1 induces an inflammatory CD4+CD8+ T cell population in HTLV-1-associated myelopathy
• HTLV-1 p12 modulates the levels of prion protein (PrP^C) in CD4⁺ T cells
• HTLV-1 Proviral Load Absolute RT-qPCR Development for Assessing on Clinical Outcomes in HAM/TSP Patients
• HTLV-1 reverse transcriptase homology model provides structural basis for sensitivity to existing nucleoside/nucleotide reverse transcriptase inhibitors
• HTLV-1 vaccination Landscape: Current developments and challenges
• HTLV-1-associated myelopathy in Spain
• HTLV-1/2 infection in Italy: a narrative review of epidemiological studies
• Human T-cell lymphotropic virus type 1 (HTLV-1) grip on T-cells: investigating the viral tapestry of activation
• Hyperargininemia: A Rare Diagnosis in Adulthood
• I¹²³-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review
• IL-10 predicts incident neuroinflammatory disease and proviral load dynamics in a large Brazilian cohort of people living with human T-lymphotropic virus type 1
• Imbalanced IL10/TGF-beta production by regulatory T-lymphocytes in patients with HTLV-1-associated myelopathy/ tropical spastic paraparesis
• Impact of video vector analysis of ankle foot orthoses in children with physical disability: A 10-year clinical review
• Infective dermatitis associated with human T-cell lymphotropic virus type-1, an underdiagnosed disease
• Intramedullary Spinal Epidermoid Cyst-A Rare Cause of Spastic Paraparesis
• Intrathecal baclofen for the management of hereditary spastic paraparesis: a systematic review
• KIF1A gene-associated neurological disease: the correlation between genotype and phenotype
• Lived Experience of Human T-cell Leukemia Virus type-1 -Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP): A Phenomenology Study
• Liver Transplantation Reverses Hepatic Myelopathy in the Decompensated Phase of Cirrhosis: Case Report and Literature Review
• Long-Term Recurrent Intramedullary Arachnoid Cyst: Case Report and Literature Review
• Movement disorders in hereditary spastic paraplegias
• Multicenter, randomized, double-blind, placebo-controlled phase 3 study of mogamulizumab with open-label extension study in a minimum number of patients with human T-cell leukemia virus type-1-associated myelopathy
• Mycophenolate mofetil for the long-term treatment of HTLV-1 associated myelopathy: A case report
• Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations
• Neurological aspects of HTLV-1 infection: symptoms in apparently asymptomatic carriers
• Non-cancerous complications in HTLV-1 carriers
• Nonpharmacological interventions and outcomes in the management of complications of human T-cell lymphotropic virus type 1-related myelopathy/tropical spastic paraparesis: A systematic review
• Novel genetic variant in hereditary spastic paraparesis
• Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)
• Novel insights into human T-lymphotropic virus type-1 (HTLV-1) pathogenesis-host interactions in the manifestation of HTLV-1-associated myelopathy/tropical spastic paraparesis
• Nucleotide metabolism, leukodystrophies, and CNS pathology
• Physiotherapy Methods Applied in the Prevention of Functional Loss Associated with Human T-Lymphotropic Virus 1 Infection: An Overview
• Prevalence and Classification of Pediatric Neuromuscular Disorders in the Central Region of Portugal
• Prevalence of Neurolathyrism and its associated factors in Grass pea cultivation areas of Dawunt District, North-eastern Ethiopia; 2022: a community based multilevel analysis
• Primary lateral sclerosis associated with PSEN1 Pro284Leu variant in a Colombian family: Clinical and neuropathological features
• Remarkable improvement of neurological deficits after surgery in patients with Idiopathic spinal cord herniations. The impact of peroperative neuromonitoring. Case reports
• RNASEH2B Pathogenic Mutation Presenting with Pure, Apparently Non-Progressive Hereditary Spastic Paraparesis
• Role of Interleukin-17 cytokine family in human T-cell lymphotropic virus type 1 (HTLV-1) infection and associated diseases
• SERAC1 Deficiency- A New Phenotype
• Spastic Paraparesis - A Rare Cause
• Spastic Paraparesis in Donnai-Barrow Syndrome: A Rare Case Report from India
• Spinal cord motor disorders
• Spinal Intramedullary Meningiomas: A Systematic Review with a Case Illustration
• Spinal lymphangiomas: Case-based review of a chameleonic disease entity
• Surgical management of a thoraco-lumbar extradural cyst in a pediatric patient with Klippel-Trenaunay syndrome: a case report
• Surgical Outcomes of Laminectomy, Durotomy and a Non-Synthetic Dura Substitute Application in Ten Dogs with a Spinal Subarachnoid Diverticulum
• T helper type 9 cell response and its role in the neurological clinic of patients with Human T-lymphotropic virus 1
• Teaching NeuroImage: Vertebrobasilar Dolichoectasia Presenting as Spastic Paraparesis
• Teaching Video NeuroImage: HTLV-1-Associated Myelopathy With Downbeat Nystagmus
• The hereditary spastic paraplegias
• The tyrosine kinase KDR is essential for the survival of HTLV-1-infected T cells by stabilizing the Tax oncoprotein
• Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis: A Case Report
• Unsatisfactory Neurological Outcome in an Intramedullary Thoracic Intermediate-Grade Melanocytoma-Systematic Review and Illustrative Case
• Viral Immune signatures from cerebrospinal fluid extracellular vesicles and particles in HAM and other chronic neurological diseases