Introduction: Oligodendroglioma is a rare, slow-growing glioma originating from oligodendrocytic cells and primarily affects adults. According to the 5th edition of the World Health Organization Classification of Tumors of the Central Nervous System, a definitive diagnosis requir...
Open access
Research Article10.9734/ajorrin/2026/v9i1169
Adekunle Fatai MUSTAPHA, Michael Bimbo FAWALE, Chiyememma Claire WORLU, Toluwalope David OYETUNDE, Aaron ThankGod UKA & Oluwadamilola Opeyemi ADENEKAN-OKONJI·Asian Journal of Research and Reports in Neurology·2026
Background: Access to anti-epileptic drugs (AEDs) remains a major challenge in low- and middle-income countries, despite significant advancements in epilepsy therapy. Availability of both older and newer AEDs varies widely across regions, and limited access contributes to poor se...
Open access
Research Article10.9734/ajorrin/2026/v9i1166
Chemotherapy-induced peripheral neuropathy (CIPN) is a frequent and clinically significant adverse effect associated with several commonly used chemotherapeutic agents, including platinum compounds, taxanes, vinca alkaloids, and proteasome inhibitors (Cavaletti and Marmiroli, 201...
Open access
Research Article10.9734/ajorrin/2026/v9i1167
Rajagiri Triveni, Koppula Sirisha, Lingineni Mani Deepa Chandrika, Nalam Vineela Nirmala, Singuluri Monica, Motupalli Poojitha & Konagala Arudra·Asian Journal of Research and Reports in Neurology·2026
Cauda Equina Syndrome (CES) is a very unusual and highly critical emergency in surgery, which is a result of the compression of nerve roots in the lumbar-spinal region and the thalamus, which could have irreversible neurological impairments in case it is not addressed in due time...
Open access
Research Article10.9734/ajorrin/2026/v9i1165
Aims: To emphasize the diagnostic challenge of primary cervical medulloblastoma mimicking a nerve sheath tumor in pediatric patients. Case Report: An 8-year-old boy presented with posterior neck swelling and spastic quadriparesis. MRI revealed a well-defined intradural extramedul...
Open access
Research Article10.9734/ajorrin/2026/v9i1164
Background: Charcot–Marie–Tooth disease type II (CMT2) is an inherited axonal sensorimotor neuropathy with heterogeneous and often subtle manifestations in early childhood. Delayed recognition may limit opportunities for timely preventive rehabilitation and early functional optim...
Open access
Research Article10.9734/ajorrin/2026/v9i1163
Aims: This systematic review aimed to critically evaluate the influence of post-translational modifications (PTMs) on α-synuclein structure, aggregation, and toxicity, and to clarify their relevance to the pathogenesis of Parkinson’s disease, dementia with Lewy bodies, and multip...
Open access
Research Article10.9734/ajorrin/2026/v9i1162
Background: Glioblastoma Multiforme (GBM) presents significant diagnostic and therapeutic challenges due to its complex molecular pathogenesis. Current diagnostic methods often fail to detect early molecular signatures critical for timely intervention. This study integrates micro...
Open access
Research Article10.9734/ajorrin/2025/v9i1161
Introduction: Precision neurorehabilitation represents a fundamental paradigm shift away from standardized, protocol-driven treatment toward dynamically adaptive therapies tailored to the unique biological and functional profiles of individual patients. The recognized high degree...
Open access
Research Article10.9734/ajorrin/2025/v8i1160
Background: Osmotic Demyelination Syndrome (ODS) is a rare neurological disorder typically linked to rapid correction of hyponatremia, but its occurrence due to hypernatremia, especially in the postpartum period, is exceedingly uncommon. Case Presentation: A 23-year-old woman, 14...
Open access
Research Article10.9734/ajorrin/2025/v8i1159